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  • 301
    Electronic Resource
    Electronic Resource
    New York, N.Y. : Wiley-Blackwell
    Journal of Cellular Biochemistry 70 (1998), S. 338-345 
    ISSN: 0730-2312
    Keywords: sphingosine ; interleukin-6 ; osteoblast ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: We previously reported that prostaglandin (PG)E1 and PGF2α induce the synthesis of interleukin-6 (IL-6) via activation of protein kinase (PK)A and PKC, respectively, in osteoblast-like MC3T3-E1 cells. In addition, we have shown that basic fibroblast growth factor (bFGF) elicits IL-6 synthesis through intracellular Ca2+ mobilization in these cells and that tumor necrosis factor-α (TNF) induces IL-6 synthesis through sphingosine 1-phosphate produced by sphingomyelin hydrolysis. In the present study, among sphingomyelin metabolites, we examined the effect of sphingosine on IL-6 synthesis induced by various agonists in MC3T3-E1 cells. Sphingosine inhibited the IL-6 synthesis induced by PGF2α or 12-O-tetradecanoylphorbol-13-acetate, an activator of PKC. Sphingosine suppressed the PGE1-induced IL-6 synthesis. The IL-6 synthesis induced by cholera toxin, forskolin, or dibutyryl cAMP was inhibited by sphingosine. Sphingosine inhibited the IL-6 synthesis induced by bFGF or A23187. However, sphingosine did not affect the IL-6 synthesis induced by interleukin-1. On the contrary, sphingosine enhanced the TNF-induced IL-6 synthesis. DL-threo-Dihydrosphingosine, an inhibitor of sphingosine kinase, reduced the enhancement by sphingosine as well as the TNF-effect. These results indicate that sphingosine modulates the IL-6 synthesis stimulated by various agonists in osteoblasts. J. Cell. Biochem. 70:338-345. © 1998 Wiley-Liss, Inc.
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  • 302
    ISSN: 0730-2312
    Keywords: cadherin ; catenins ; thyroid carcinoma cell ; epithelial cell ; cell-cell adhesion ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: E-cadherin is the major cell-cell adhesion molecule expressed by epithelial cells. Cadherins form a complex with three cytoplasmic proteins, α-, β-, and γ-catenin, and the interaction between them is crucial for anchoring the actin cytoskeleton to the intercellular adherens junctions. The invasive behavior of cancer cells has been attributed to a dysfunction of these molecules. In this study, we examined the distribution of the cadherin-catenin complex in a Chinese human thyroid cancer cell line, CGTH W-2, compared with that in normal human thyroid epithelial cells. In the normal cells, using immunofluorescence staining, E-cadherin and α-, β-, and γ-catenin were found to be localized at the intercellular junction and appeared as 135, 102, 90, and 80 kD proteins on Western blots. In CGTH W-2 cells, no E-cadherin and γ-catenin immunoreactivity was detected by immunofluorescence or Western blotting; α- and β-catenin were detected as 102 and 90 kD proteins on blots but gave a diffuse cytoplasmic immunofluorescence staining pattern in most cells, while β-catenin was also distributed throughout the cytoplasm in most cells but was found at the cell junction in some, where it colocalized with α-actinin. The present data indicate that the loss of cell adhesiveness in these cancer cells may be due to incomplete assembly of the cadherin-catenin complex at the cell junction. However, this defect did not affect the linkage of actin bundles to vinculin-enriched intercellular junctions. J. Cell. Biochem. 70:330-337, 1998. © 1998 Wiley-Liss, Inc.
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  • 303
    Electronic Resource
    Electronic Resource
    New York, N.Y. : Wiley-Blackwell
    Journal of Cellular Biochemistry 70 (1998), S. 433-441 
    ISSN: 0730-2312
    Keywords: AKT2 ; serine-threonine kinase ; oncogene ; insulin ; phosphatidylinositol 3-kinase ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: The AKT2 oncogene encodes a protein-serine/threonine kinase that was recently shown to be activated by a variety of growth factors. In addition, we previously showed that AKT2 is abundant in brown fat and skeletal muscle, tissues that are highly insulin responsive and that play a role in glucose metabolism. In this study, we demonstrate that AKT2 is activated in response to stimulation by insulin in a dose- and time-dependent manner in human ovarian carcinoma cells and that activation of AKT2 is abolished in cells pretreated with wortmannin, an inhibitor of phosphatidylinositol 3-kinase (PI 3-kinase). Activation of AKT2 is manifested by changes in its phosphorylation state. Immunofluorescence experiments demonstrate that AKT2 is translocated to the plasma membrane after insulin stimulation, and this translocation is abolished by wortmannin. Both wild-type AKT2 activated by insulin and constitutively active AKT2, which has been targeted to the membrane by the addition of a myristoylation signal, were found to inactivate glycogen synthase kinase-3 (GSK-3) in vitro. GSK-3 was not inactivated by a catalytically inactive AKT2 mutant. Collectively, these data indicate that activation of AKT2 by insulin is mediated by PI 3-kinase and that GSK-3 is a downstream target of AKT2, suggesting a potentially important role of AKT2 in glycogen synthesis and other GSK-3 signaling pathways. J. Cell. Biochem. 70:433-441, 1998. © 1998 Wiley-Liss, Inc.
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  • 304
    Electronic Resource
    Electronic Resource
    New York, N.Y. : Wiley-Blackwell
    Journal of Cellular Biochemistry 70 (1998), S. 425-432 
    ISSN: 0730-2312
    Keywords: nerve growth factor ; tyrosine kinase receptors ; differentiation ; PC12 cells ; mitogen-activated protein kinase ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Activation of receptor tyrosine kinases stimulates a diverse array of cellular responses such as proliferation and differentiation. The first events in the signal transduction pathways mediated by different receptor tyrosine kinases are similar and include activation of the mitogen-activated protein kinase (MAPK) pathway and the induction of immediate early genes. The precise signaling pathways leading to each of the cellular responses mediated by receptor tyrosine kinases are still unknown, although it has been proposed that sustained activation of the MAPK pathway by receptor tyrosine kinases such as the nerve growth factor (NGF) receptor TrkA is sufficient to induce differentiation in PC12 cells. In the present study we examined the effect of NGF on mutant PC12 cells that were derived spontaneously in our cultures. NGF induced normal activation of immediate early genes in these cells, whereas the activation of some delayed response genes, as well as neurite outgrowth, was impaired. Furthermore, activation of the NGF-induced extracellular signal-regulated kinase (ERK) in these cells was transient, not sustained. These results support the hypothesis that sustained activation of ERK plays an important role in activating the induction of delayed response genes. However, sustained ERK activation is not a mandatory condition for the promotion of all the features of differentiated PC12 cells, as NGF could induce transcription of the delayed response gene, transin, in PC12 mutant cells. Taken together, our results suggest that NGF induces differentiation of PC12 cells via several signaling pathways, an important one of which is the MAPK pathway. J. Cell. Biochem. 70:425-432, 1998. © 1998 Wiley-Liss, Inc.
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  • 305
    Electronic Resource
    Electronic Resource
    New York, N.Y. : Wiley-Blackwell
    Journal of Cellular Biochemistry 70 (1998), S. 455-467 
    ISSN: 0730-2312
    Keywords: collagen ; gene regulation ; DNA-binding proteins ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Both the mouse and human α2(I) procollagen promoters contain an inverted CCAAT box at -80, but only the human promoter contains an additional regulatory element, the collagen modulating element (CME), immediately downstream of the CCAAT box [Collins et al. (1997): Biochem J 322:199-206]. In this study, the transcription factors that bind to the G/CBE and CME within the human promoter were characterized in SVWI-38 and CT-1 nuclear extracts. Two distinct proteins bind to the CME, and both were identified as heat-labile factors that were sensitive to high ionic strengths and required Zn2+ for DNA-binding activity. These proteins had Stokes radii of 4.12 and 3.15 nm, sedimentation coefficients of 3.9 and 3.2 S and native molecular weights of 66 and 41 kDa, respectively. On the basis of biochemical and DNA-binding properties, the CME binding proteins are probably novel factors involved in the regulation of the human α2(I) procollagen gene. By contrast, the G/CBE binding proteins were more resistant to heat, ionic strength, and divalent metal ion chelators, demonstrating that the G/CBE and CME binding proteins had distinct DNA-binding properties. The above properties suggest that this factor is a member of the previously characterized family of CCAAT box-binding factors, CBF, NF-Y, CP-1 and α-CP1. Taken together, these physicochemical properties of the COL1A2 CCAAT box and CME-binding proteins demonstrated that they were distinct unrelated transcription factors. These results also suggest that there is a distinct difference in the DNA-binding activity between the equivalent region of the mouse and human α2(I) procollagen promoters. J. Cell. Biochem. 70:455-467, 1998. © 1998 Wiley-Liss, Inc.
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  • 306
    Electronic Resource
    Electronic Resource
    New York, N.Y. : Wiley-Blackwell
    Journal of Cellular Biochemistry 70 (1998), S. 442-454 
    ISSN: 0730-2312
    Keywords: UV irradiation ; PAK2 ; apoptosis ; CPP32/caspase-3 ; A431 cells ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Exposure of mammalian cells to ultraviolet (UV) light elicits a cellular response and can also lead to apoptotic cell death. In this report, we show that a 36-kDa myelin basic protein (MBP) kinase detected by an in-gel kinase assay can be dramatically activated during the early stages of UV irradiation-triggered apoptosis of A431 cells. Immunoblot analysis revealed that this 36-kDa MBP kinase could be recognized by an antibody against the C-terminal regions of a family of p21Cdc42/Rac-activated kinases (PAKs). By using this antibody and a PAK2-specific antibody against the N-terminal region of PAK2 as studying tools, we further demonstrated that UV irradiation caused cleavage of PAK2 to generate a 36-kDa C-terminal catalytic fragment and a 30-kDa N-terminal fragment in A431 cells. The appearance of the 36-kDa C-terminal catalytic fragment of PAK2 matched exactly with the activation of the 36-kDa MBP kinase in A431 cells upon UV irradiation. In addition, UV irradiation also led to activation of CPP32/caspase-3, but not ICH-1L/caspase-2 and ICE/caspase-1, in A431 cells and the kinetics of activation of CPP32/caspase-3 appeared to correlate well with that of DNA fragmentation and of cleavage/activation of PAK2, respectively. Moreover, blockage of activation of CPP32/caspase-3 by pretreating the cells with two specific tetrapeptidic inhibitors for caspases (Ac-DEVD-cho and Ac-YVAD-cmk) could significantly attenuate the extent of cleavage/activation of PAK2 induced by UV irradiation. Collectively, the results demonstrate that cleavage and activation of PAK2 can be induced during the early stages of UV irradiation-triggered apoptosis and indicate the involvement of CPP32/caspase-3 in this process. J. Cell. Biochem. 70:442-454, 1998. © 1998 Wiley-Liss, Inc.
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  • 307
    Electronic Resource
    Electronic Resource
    New York, N.Y. : Wiley-Blackwell
    Journal of Cellular Biochemistry 70 (1998), S. 22-28 
    ISSN: 0730-2312
    Keywords: Msx-1 ; Msx-2 ; homeobox ; adhesion ; sorting ; cadherin ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Msx-1 and Msx-2 are two closely related homeobox genes expressed in cephalic neural crest tooth buds, the optic cup endocardial cushions, and the developing limb [Hill and Davidson, 1991; Monaghan et al., 1991; Robert et al., 1991]. These sites correspond to regions of active cell segregation and proliferation under the influence of epithelial-mesenchymal cell interactions [Brown et al., 1993; Davidson et al., 1991], suggesting that Msx-1 and Msx-2 regulate cell-cell interactions. We have investigated the potential relationship between expression of the Msh homeobox genes (Msx-1 and Msx-2) and cadherin-mediated cell adhesion and cell sorting. We report that cell lines stably expressing Msx-1 or Msx-2 differentially sort on the basis of Msh gene expression. We demonstrate in vitro that initial cell aggregation involves calcium-dependent adhesion molecules (cadherins) and that Msh genes regulate cadherin-mediated adhesion. These results support the hypothesis that Msh genes play a role in the regulation of cell-cell adhesion and provide a link between the genetic phenomena of homeobox gene expression and cellular events involved in morphogenesis, including cell sorting and proliferation. J. Cell. Biochem. 70:22-28, 1998. © 1998 Wiley-Liss, Inc.
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  • 308
    Electronic Resource
    Electronic Resource
    New York, N.Y. : Wiley-Blackwell
    Journal of Cellular Biochemistry 70 (1998), S. 38-48 
    ISSN: 0730-2312
    Keywords: GABAA receptor ; N-glycosylation ; radioligand binding ; in situ trypsinization ; galactosylation ; mannosylation ; immunoblotting ; immunocytochemistry ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: The significance of N-linked glycosylation and oligosaccharide processing was examined for the expression of γ-aminobutyric acidA receptor (GABAAR) in cultured neurons derived from chick embryo brains. Incubation of cultures with 5 μg/ml of tunicamycin for 24 h blocked the binding of 3H-flunitrazepam and 3H-muscimol, probes for the benzodiazepine and GABA sites on the receptor, by about 20% and 28%, respectively. The loss of ligand binding was due to a reduction in the number of binding sites with no significant changes in receptor affinity. Light microscopic immunocytochemistry also revealed that the treatment reduced approximately 13% of the intensity of GABAAR immunoreactivity in the neuronal somata. Furthermore, the fraction of intracellular receptors was decreased to 24% from 34% of control in the presence of the agent, as revealed by trypsinization of cells in situ followed by 3H-flunitrazepam binding. The molecular weight of the receptor subunit protein was lowered around 0.5 kDa after tunicamycin treatment, in accordance with that following N-glycosidase F digestion, indicating the blockade of N-linked glycosylation of GABAAR by tunicamycin. Moreover, intense inhibitions of 91% and 44%, respectively, were detected to the general galactosylation and mannosylation in the tunicamycin-treated cells, whereas the protein synthesis was hindered by 13%, through assaying the incorporation of 3H-sugars and 3H-leucine. Nevertheless, treatment with castanospermine or swainsonine (10 μg/ml, 24 h), inhibitors to maturation of oligosaccharides, failed to produce significant changes in the ligand binding. In addition, in situ hybridization analysis showed that these three inhibitors did not perturb the mRNA of GABAAR α1-subunit. The data suggest that tunicamycin causes the downregulation and subcellular redistribution of GABAAR by producing irregularly glycosylated receptors and modifying their localization. Both galactosylation and mannosylation during the process of N-linked glycosylation may be important for the functional expression and intracellular transport of GABAAR. J. Cell. Biochem. 70:38-48, 1998. © 1998 Wiley-Liss, Inc.
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  • 309
    Electronic Resource
    Electronic Resource
    New York, N.Y. : Wiley-Blackwell
    Journal of Cellular Biochemistry 70 (1998), S. 60-69 
    ISSN: 0730-2312
    Keywords: opossum kidney cells ; opioid receptors ; actin ; microfilament reorganization ; cell proliferation ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Recently we identified and characterized opioid binding sites in OK (opossum kidney) cells and observed decreased proliferation of these cells in response to opioids. In the present study we investigated the effects of opioids on the actin cytoskeleton and explored whether their antiproliferative action may relate to alterations in the distribution or the dynamics of actin microfilaments. Exposure of OK cells to the opioids αS1 casomorphin and ethylketocyclazocine resulted in a rapid and substantial actin microfilament reorganization. This was documented by a significant dose-dependent decrease in the amounts of F-actin, determined by measurements of quantitative fluorescence, by immunoblot analysis and by a concomitant increase of the G/total-actin ratio measured by the DNase I inhibition assay. These changes were verified by confocal laser scanning microscopy, which showed marked redistribution of the microfilamentous structures in the presence of the opioids without affecting the organization of microtubules or vimentin intermediate filaments. The effect of opioids on actin polymerization dynamics occurred within 15 min and persisted for at least 2 h, while their restoration to control levels was accomplished 6 h later, indicating a reversible phenomenon. Northern blot analysis showed that the concentration of the actin transcript was unaffected. The addition of diprenorphine, a general opioid antagonist, prevented the effects of opioids on the actin cytoskeleton. The inhibition of OK cell proliferation, induced by ethylketocyclazocine and αS1 casomorphin was partially prevented in the presence of phallacidin, which stabilizes microfilaments. Our findings demonstrate that opioids, acting via kappa 1 binding sites, induce rapidly modifications in the dynamics of actin polymerization, and in the organization of microfilaments in OK cells, which may relate to their antiproliferative effect on these cells. J. Cell. Biochem. 70:60-69, 1998. © 1998 Wiley-Liss, Inc.
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  • 310
    ISSN: 0730-2312
    Keywords: arthritis ; cartilage ; gene regulation ; kinases ; signaling ; tissue inhibitors of metalloproteinases ; transforming growth factor beta ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: The balance between matrix metalloproteinases (MMPs) and tissue inhibitors of metalloproteinases (TIMPs) regulates extracellular matrix turn-over in normal animal development, cancer cell metastasis, atherosclerotic plaque rupture and erosion of arthritic cartilage. Transforming growth factor beta (TGF-β), an inducer of matrix synthesis, potently enhances mRNA and protein of a recently characterized MMP inhibitor, TIMP-3, in bovine articular chondrocytes. We examined the implication of protein kinases in the TGF-β-mediated induction of TIMP-3 expression by utilizing activators and inhibitors of these enzymes. Protein kinase A activators, dibutyryl cyclic AMP, or forskolin had little or no effect, respectively, while phorbol 12-myristate 13-acetate (PMA), a PKC activator, increased TIMP-3 gene expression. H7, a serine/threonine protein kinase inhibitor, markedly reduced the response of TIMP-3 gene to TGF-β. Furthermore, two protein tyrosine kinase inhibitors, genistein and herbimycin A, inhibited TGF-β induction of TIMP-3. H7 and genistein also suppressed TGF-β-induced TIMP-3 protein expression. These results suggest that TGF-β signaling for TIMP-3 gene induction involves H7-sensitive serine/threonine kinase as well as herbimycin A- and genistein-sensitive protein tyrosine kinases. J. Cell. Biochem. 70:517-527, 1998. © 1998 Wiley-Liss, Inc.
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  • 311
    Electronic Resource
    Electronic Resource
    New York, N.Y. : Wiley-Blackwell
    Journal of Cellular Biochemistry 70 (1998), S. 478-488 
    ISSN: 0730-2312
    Keywords: osteoporosis ; osteopenia ; aging ; bone formation ; growth factors ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: One of the universal characteristics of the long bones and spines of middle-age and older mammals is a loss in bone mass (osteopenia). In humans, if this bone loss is severe enough, it results in osteoporosis, a skeletal disorder characterized by a markedly increased incidence of fractures with sequelae that may include pain, loss of mobility, and in the event of hip fracture, even death within a relatively few months of injury. An important contributing factor to the development of osteopororsis appears to be a diminution in the number and activity of osteoblasts responsible for synthesizing new bone matrix. The findings in the present and other similar studies suggest that this reduction in osteoblast number and activity is due to an age-related diminution in the size and osteogenic potential of the bone marrow osteoblast progenitor cell (OPC or CFU-f) compartment. We previously postulated that these regressive changes in the OPC/CFU-f compartment occurred in old animals because of a reduction in the amount and/or activity of TGF-β1, an autocrine growth factor important in the promotion of OPC/CFU-f proliferation and differentiation. In support of this hypothesis, we now report that (1) the osteogenic capacity of the bone marrow of 24-month-old BALB/c mice, as assessed in vivo, is markedly reduced relative to that of 3-4-month-old animals, (2) that the matrix of the long bones of old mice contains significantly less TGF-β than that of young mice, (3) that OPC's/CFU-f's isolated from old mice produce less TGF-β in vitro than those recovered from young mice, and (4) that OPC's/CFU-f's from old mice express significantly more TGF-β receptor (Types I, II, and III) than those of young animals and that such cells are more responsive in vitro to exogenous recombinant TGF-β1. We also find that colony number and proliferative activity of OPC's/CFU-f's of young mice and old mice, respectively, are significantly reduced when incubated in the presence of neutralizing TGF-β1 antibody. Collectively, these data are consistent with the hypothesis that in old male mice the reduction in the synthesis and, perhaps, availability from the bone matrix of TGF-β1 contributes to a diminution in the size and development potential of the bone marrow osteoprogenitor pool. J. Cell. Biochem. 70:478-488. © 1998 Wiley-Liss, Inc.
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  • 312
    Electronic Resource
    Electronic Resource
    New York, N.Y. : Wiley-Blackwell
    Journal of Cellular Biochemistry 70 (1998), S. 528-542 
    ISSN: 0730-2312
    Keywords: c-Myc ; Cdk ; Cdk inhibitors ; keratinocytes ; cell cycle ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: The function of the c-myc proto-oncogene in cell cycle progression remains unclear. In order to examine the role c-myc may play in cell cycle progression, we have expressed the hormone-inducible MycER protein in the nontransformed, EGF-dependent mouse keratinocyte cell line BALB/MK. We have found that activation of MycER, but not a mutant MycER, Gal4ER, or FosER, leads to an EGF-dependent and hormone-dependent increased incorporation of labeled thymidine only during the S phase of the cell cycle in BALB/MK cells. A possible explanation for the increase in thymidine incorporation comes from flow cytometric analyses that reveal that activation of MycER leads to an increase in the total number of cells that enter S phase after EGF restimulation. Investigation of the intracellular effects of Myc activation shows that the expression of several putative Myc-sensitive proteins, cyclins A, E, and D1, and the E2F-1 protein are unaffected by Myc induction. Interestingly, we find that the histone H1 kinase activity associated with an E2F-1 complex containing Cyclin A and Cdk-2, but not that associated with Cyclin E, in late G1 and early S phases is increased in cells containing hormone-activated MycER, but not FosER. Although the mechanism for this Myc-dependent effect on E2F-1-associated kinase activity is still unknown, it does not appear to involve dissociation of the Cdk inhibitor p27Kip1 from the complexes as suggested by others. However, we have also found that hormone-treated cells actually show more p16INK4A inhibitor associated with another kinase, Cdk-4, as the cells are entering S phase. Altogether, the data suggest that the presence of excessive Myc protein in keratinocytes can stimulate otherwise noncycling cells to enter the cell cycle, and that this effect of Myc involves both positive effects on E2F-1-associated Cdk-2 and negative effects on Cdk-4 in late G1. J. Cell Biochem. 70:528-542, 1998. © 1998 Wiley-Liss, Inc.
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  • 313
    Electronic Resource
    Electronic Resource
    New York, N.Y. : Wiley-Blackwell
    Journal of Cellular Biochemistry 70 (1998), S. 543-552 
    ISSN: 0730-2312
    Keywords: SPARC ; endothelial cell ; cell spreading ; focal adhesion ; actin ; vinculin ; PTK inhibitors ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: SPARC, a counteradhesive matricellular protein, inhibits endothelial cell adhesion and proliferation, but the pathways through which these activities are blocked are not known. In this study, we used inhibitors of major signaling proteins to identify mediators through which SPARC exerts its counteradhesive and antiproliferative functions. Pretreatments with the general protein tyrosine kinase (PTK) inhibitors, herbimycin A and genistein, protected against the inhibitory effect of SPARC on bovine aortic endothelial (BAE) cell spreading by more than 60 %. Similar pretreatments with PTK inhibitors significantly blocked the diminishment of focal adhesions by SPARC in confluent BAE cell monolayers, as determined by the formation of actin stress-fibers and the distribution of vinculin in focal adhesion plaques. Inhibition of endothelial cell cycle progression by SPARC and a calcium-binding SPARC peptide, however, was not affected by PTK inhibitors. Inhibition of DNA synthesis by SPARC was not reversed by inhibitors of the activity of protein kinase C (PKC), or of cAMP-dependent protein kinase (PKA), but was sensitive to pertussis (and to a lesser extent, cholera) toxin. The counteradhesive effect of SPARC on endothelial cells is, therefore, mediated through a tyrosine phosphorylation-dependent pathway, whereas its antiproliferative function is dependent, in part, on signal transduction via a G protein-coupled receptor. J. Cell. Biochem. 70:543-552, 1998. © 1998 Wiley-Liss, Inc.
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  • 314
    Electronic Resource
    Electronic Resource
    New York, N.Y. : Wiley-Blackwell
    Journal of Cellular Biochemistry 70 (1998), S. 553-562 
    ISSN: 0730-2312
    Keywords: coimmunoprecipitation of Gβ subunit and tubulin ; in situ incorporation of Gβ protein into microtubules ; microtubule assembly ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Previously, we have identified the association of G protein β subunit (Gβ) with mitotic spindles in various mammalian cells. Since microtubules are the main component of mitotic spindles, here we have isolated bovine brain microtubules and purified Gβ subunit to identify the close association of Gβ subunit with purified brain microtubules and have shown the direct incorporation of Gβ subunit into the microtubules both in vitro and in vivo. It was found that: (1) microtubular fraction isolated from bovine brain contained Gβ subunit, (2) coimmunoprecipitation demonstrated that Gβ subunit could be coprecipitated with tubulin, (3) addition of purified Gβ subunit into cytosolic extract for microtubule assembly caused direct incorporation of Gβ subunit into assembled microtubules and increased the association of microtubule-associated proteins with microtubules, and (4) incubation of exogenous Gβ subunit with detergent-permeabilized cells resulted in direct incorporation of Gβ subunit into microtubule fibers and depolymerized tubulin molecules. We conclude that G protein β subunit is closely associated with microtubules and may play an important role in the regulation of microtubule formation in addition to its regulatory role in cellular signal transduction. J. Cell. Biochem. 70:553-562, 1998. © 1998 Wiley-Liss, Inc.
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  • 315
    ISSN: 0730-2312
    Keywords: breast carcinoma ; ERK pathway ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: The AU565 breast carcinoma cell line was used to determine the role of the extracellular-regulated kinase (ERK) pathway in mediating Heregulinβ1 (HRGβ1)-induced mammary cell differentiation. ERK activation remained elevated for 2 h following high doses of HRG which induce differentiation. In contrast, a transient 5 min peak of ERK activation in response to doses of HRG which induce proliferation was observed. A MEK specific inhibitor, PD98059, which inhibited activation of ERK in response to HRG, completely blocked HRG-induced differentiation and reversed cell growth arrest. To further assess the importance of sustained ERK activity in cellular differentiation, we transiently transfected a mutant constitutively active MEK1 construct into AU565 cells. Differentiation was induced in the absence of HRG and treatment with HRG potentiated this response. These data indicate that sustained activation of the MEK/ERK pathway is both essential and sufficient for HRG-induced differentiation of AU565 cells. J. Cell. Biochem. 70:587-595, 1998. © 1998 Wiley-Liss, Inc.
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  • 316
    ISSN: 0730-2312
    Keywords: heparan sulfate and growth factors ; heparan sulfate and phorbol ester ; heparan sulfate and cell cycle ; proteoglycans and cell cycle ; cell cycle; phorbol ester and heparan sulfate ; heparan sulfate and PKC ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Fetal calf serum (FCS) and PMA (phorbol 12-myristate-13-acetate) specifically stimulate the synthesis of heparan sulfate proteoglycan in endothelial cells. Staurosporine and n-butanol, kinase inhibitors, abolish the PMA effect. Forskolin and 8-bromo adenosine 3′:5′-cyclic monophosphate, activators of, respectively, adenylate cyclase and protein kinase A cannot reproduce the PMA effect. The kinetics of cell entry into S phase of the endothelial cells was determined by DNA synthesis ([3H]-thymidine and Br-dU incorporation), and flow cytometry. The mitogenic effect of fetal calf serum is abolished by PMA. Also, PMA pre-treatment inhibits the enhanced synthesis of heparan sulfate proteoglycan after a second PMA exposure. Remarkably, the stimulation of heparan sulfate proteoglycan synthesis by fetal calf serum and PMA seems to be mainly restricted to G1 phase. Therefore fetal calf serum and PMA cause an enhanced synthesis of heparan sulfate proteoglycan, and PMA causes a cell cycle block at G1 phase. J. Cell. Biochem. 70:563-572, 1998. © 1998 Wiley-Liss, Inc.
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  • 317
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    Journal of Cellular Biochemistry 71 (1998), S. 491-501 
    ISSN: 0730-2312
    Keywords: diabetic microangiopathy ; endothelium ; HMEC-1 ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Diabetic microangiopathy has been implicated as a fundamental feature of the pathological complications of diabetes including retinopathy, neuropathy, and diabetic foot ulceration. However, previous studies devoted to examining the deleterious effects of elevated glucose on the endothelium have been performed largely in primary cultured cells of macrovessel origin. Difficulty in the harvesting and maintenance of microvascular endothelial cells in culture have hindered the study of this relevant population. Therefore, the objective of this study was to characterize the effect of elevated glucose on the proliferation and involved signaling pathways of an immortalized human dermal microvascular endothelial cell line (HMEC-1) that possess similar characteristics to their in vivo counterparts. Human dermal microvascular endothelial cells (HMEC-1) were grown in the presence of normal (5 mM) or high D-glucose (20 mM) for 14 days. The proliferative response of HMEC-1 was compared under these conditions as well as the cAMP and PKC pathways by in vitro assays. Elevated glucose significantly inhibited (P 〈 0.05) HMEC-1 proliferation after 7, 10, and 14 days. This effect was not mimicked by 20 mM mannitol. The antiproliferative effect was more pronounced with longer exposure (1-14 days) to elevated glucose and was irreversible 4 days after a 10-day exposure. The antiproliferative effect was partially reversed in the presence of a PKA inhibitor, Rp-cAMP (10-50 μM), and/or a PKC inhibitor, Calphostin C (10 nM). HMEC-1 exposed to elevated glucose (20 mM) for 14 days caused an increase in cyclic AMP accumulation, PKA, and PKC activity but was not associated with the activation of downstream events such as CRE and AP-1 binding activity. These data support the hypothesis that HMEC-1 is a suitable model to study the deleterious effects of elevated glucose on microvascular endothelial cells. Continued studies with HMEC-1 may prove advantageous in delineation of the molecular pathophysiology associated with diabetic microangiopathy. J. Cell. Biochem. 71:491-501, 1998. © 1998 Wiley-Liss, Inc.
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  • 318
    ISSN: 0730-2312
    Keywords: HMG-CoA ; MVA ; HPLC ; dolichol-like lipids ; DNA synthesis ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Substantial evidence has suggested that a nonsterol product of mevalonic acid (MVA) is essential for the initiation of DNA synthesis in mammalian cells. Several possible isoprenoid candidates have been suggested, but the identity of this compound still remains unknown. In this study we have isolated and purified MVA products from SV40-transformed human fibroblasts and identified fractions with a growth-stimulatory effect. The cells were labelled with [14C]MVA in the presence of inhibitors of 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase. After lipid extraction, the [14C]MVA-labelled lipids were subjected to high performance liquid chromatography and size-exclusion chromatography, and the effect of the fractionated eluate on the DNA synthesis of arrested MVA-depleted target cells was tested. Thereby we found a fraction of [14C]MVA-labelled lipids with a substantial stimulatory effect on DNA synthesis. The chromatographic behavior suggested that the growth-stimulating fractions contained dolichol-20. This was confirmed by mass spectrometric analysis. Similar results were obtained when lipids from hepatocellular carcinoma cells and a sample from breast tumor were isolated and analyzed by the same procedure. The mechanisms by which these compounds induce DNA synthesis are unknown. Recent data obtained in our laboratory have provided evidence that dolichyl groups are covalently linked to tumor cell proteins, which implicates a new biological function for long-chain polyisoprenoid alcohols (Hjertman et al. [1997] FEBS Lett 416:235-238). In this study we demonstrate that tumor cells containing dolichol-like growth-stimulatory lipids also contained dolichylated proteins. This raises the question whether the growth-stimulatory dolichol-like lipids serve as substrates for the dolichylation reaction. J. Cell. Biochem. 71:502-514, 1998. © 1998 Wiley-Liss, Inc.
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  • 319
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    Journal of Cellular Biochemistry 71 (1998), S. 515-523 
    ISSN: 0730-2312
    Keywords: binding ; complex formation ; retinoic X receptor ; TFIIB ; vitamin D receptor ; VDRE ; steroid receptor ; nuclear extract ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: The vitamin D receptor (VDR) elicits a transcriptional response to 1,25-dihydroxyvitamin D3 by binding to specific response elements (VDRE) in the promoter of target genes. Retinoic X receptor (RXR) is required for formation of the VDR-VDRE complex when VDR is supplied at physiologic concentrations. When porcine intestinal nuclear extract is used as a source of VDR, two distinct complexes are always observed with native gel electrophoresis. Both complexes contain VDR and RXR. We now show that the faster-migrating complex requires another heretofore unknown nuclear factor for its formation. In addition, we provide evidence that the formation of the slower-migrating complex is enhanced by transcription factor IIB (TFIIB). Using ligand binding assays, we determined that both complexes contain the same ratio of VDR to VDRE. Using RXR subtype-specific antibodies in gel shift assays, we show that the complexes contain more than one RXR subtype. Therefore, the present results demonstrate VDR-RXR-VDRE complexes formed with pig intestinal nuclear extracts contain other proteins and that the complexes formed between VDR and VDRE are not simply heterodimers of VDR and RXR. J. Cell. Biochem. 71:515-523, 1998. © 1998 Wiley-Liss, Inc.
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  • 320
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    Journal of Cellular Biochemistry 71 (1998), S. 524-535 
    ISSN: 0730-2312
    Keywords: caveolae ; caveolin-1 ; tyrosine kinase ; cell transformation ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Members of the nonreceptor tyrosine kinase family appear to be targeted to caveolae membrane. We have used a Rat-1 cell expressing a temperature sensitive pp60v-src kinase to assess the initial changes that take place in caveolae after kinase activation. Within 24-48 h after cells were shifted to the permissive temperature, a set of caveolae-specific proteins became phosphorylated on tyrosine. During this period there was a decline in the caveolae marker protein, caveolin-1, a loss of invaginated caveolae, and a 70% decline in the sphingomyelin content of the cell. One of the phosphorylated proteins was caveolin-1 but it was associated in coimmunoprecipitation assays with both a 30 kDa and a 27 kDa tyrosine-phosphorylated protein. Finally, the cells changed from having a typical fibroblast morphology to a rounded shape lacking polarity. In light of the recent evidence that diverse signaling events originate from caveolae, pp60v-src kinase appears to cause global changes to this membrane domain that might directly contribute to the transformed phenotype. J. Cell. Biochem. 71:524-535, 1998. © 1998 Wiley-Liss, Inc.
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  • 321
    ISSN: 0730-2312
    Keywords: intestinal epithelium ; cell growth ; cell differentiation ; HIEC ; Caco-2 ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: The integrin α9β1 is one of the recently identified integrins whose expression is restricted to specialized tissues. Its exact function is still unknown. In the present study, we have analyzed the expression of the α9 subunit in human fetal and adult small intestinal and colonic epithelia as well as in intestinal cell lines by indirect immunofluorescence, immunoprecipitation, Western blot, and Northern blot. In intact tissues, the antigen was restricted to the basolateral domain of epithelial cells in intestinal crypts at the fetal stage and was absent in the adult. The α9β1 integrin was also detected in the intestinal cell lines HIEC-6 and Caco-2/15. The presence of α9β1 in HIEC-6 was found to be consistent with their proliferative crypt-like status. In Caco-2/15 cells, the integrin was present at high levels in proliferating cells but was downregulated when cells cease to grow and undertake their differentiation. EGF treatment, which is known to maintain Caco-2/15 cells in a proliferative state, resulted in higher levels of α9 as compared to control cells. Taken together, these observations suggest a relation between integrin α9β1 expression and proliferation in human intestinal cells. J. Cell. Biochem. 71:536-545, 1998. © 1998 Wiley-Liss, Inc.
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  • 322
    ISSN: 0730-2312
    Keywords: matrix metalloproteinase ; sea urchin ; development ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: We have purified and characterized a collagenase/gelatinase activity expressed during sea urchin embryonic development. The native molecular mass was determined to be 160 kDa, while gelatin substrate gel zymography revealed an active species of 41 kDa, suggesting that the native enzyme is a tetramer of active subunits. Incubation in the presence of EGTA resulted in nearly complete loss of activity and this effect could be reversed by calcium. Calcium-induced reactivation appeared to be cooperative and occurred with an apparent kd value of 3.7 mM. Two modes of calcium binding to the 41-kDa subunit were detected; up to 80 moles of calcium bound with a kd value of 0.5 mM, while an additional 120 moles bound with a kd value of 5 mM. Amino acid analysis revealed a carboxy plus carboxyamide content of 24.3 mol/100 mol, indicating the availability of substantial numbers of weak Ca2+-binding sites. Calcium binding did not result in either secondary or quaternary structural changes in the collagenase/gelatinase, suggesting that Ca2+ may facilitate activation through directly mediating the binding of substrate to the enzyme. The collagenase/gelatinase activity was detected in blastocoelic fluid and in the hyalin fraction dissociated from 1-h-old embryos. Immunolocalization studies revealed two storage compartments in the egg; cortical granules and small granules/vesicles dispersed throughout the cytoplasm. After fertilization, the antigen was detected in both the apical and basal extracellular matrices, the hyaline layer, and basal lamina, respectively. J. Cell. Biochem. 71:546-558, 1998. © 1998 Wiley-Liss, Inc.
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  • 323
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    Journal of Cellular Biochemistry 71 (1998), S. 559-568 
    ISSN: 0730-2312
    Keywords: plasma cell ; CD19 ; CD38 ; naphthol AS-D chloroacetate esterase ; B cells ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: This study demonstrates that the multiple myeloma cell (MMC) in its plasma cell form is morphologically indistinguishable from human osteoclast-like cells that form in culture when peripheral blood mononuclear cells (PBMCs) are plated at high density in serum containing medium. MM has been described as a disease of B-cell lineage, monoclonal immunoglobulin (Ig) producing cells with unique properties: MM precursor cells lodge in bone, where they proliferate and differentiate into plasma cell tumors. Then, by some mechanism, presumably involving cytokines, these cells mediate an increase in neighboring osteoclast numbers and activity, leading to excessive bone erosion and hypercalcemia. Three days after plating PBMCs, tartrate resistant acid phosphatase- (TRAP-) blasts as well as TRAP+ cells, each with an eccentric nucleus, appear in culture. By day 10, TRAP+, vitronectin+ (VR+) cells, appear to be morphologically indistinguishable from multiple myeloma plasma cells (MMPCs) on cytocentrifuge preparations. These cells are CD19- and CD38++, as are MMCs reported by others. Other surface markers are also shared. Furthermore, Ig mRNA is demonstrated in the cytoplasm of cells at 8 days by in situ hybridization with the IgG FcA3 sequence. This novel finding is not unusual, in light of reports, demonstrating non-B-lineage Ig-producing cells. Thus, this study raises some serious questions about the true nature of MMCs. J. Cell. Biochem. 71:559-568, 1998. © 1998 Wiley-Liss, Inc.
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  • 324
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    Journal of Cellular Biochemistry 71 (1998), S. 569-576 
    ISSN: 0730-2312
    Keywords: regucalcin ; calmodulin ; protein kinase ; calcium-binding protein ; liver nuclei ; regenerating rat liver ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: The effect of Ca2+-binding protein regucalcin on protein kinase activity in the nuclei of normal and regenerating rat livers was investigated. Protein kinase activity in the nuclei isolated from normal rat liver was significantly increased by addition of Ca2+ (500 μM) and calmodulin (10 μg/ml) in the enzyme reaction mixture. Nuclear protein kinase activity was significantly decreased in the presence of EGTA (1.0 mM), trifluoperazine (TFP; 20 μM), dibucaine (10-4 M), or staurosporine (10-7 M), indicating that Ca2+-dependent protein kinases are present in the nuclei. Protein kinase activity was significantly elevated in the liver nuclei obtained at 6 to 48 h after a partial hepatectomy. Hepatectomy-increased nuclear protein kinase activity was significantly decreased in the presence of EGTA (1.0 mM), TFP (20 μM), or staurosporine (10-7 M) in the enzyme reaction mixture. The presence of regucalcin (0.1-0.5 μM) caused a significant decrease in protein kinase activity in the nuclei obtained from normal and regenerating rat livers. Meanwhile, the nuclear protein kinase activity from normal and regenerating livers was significantly elevated in the presence of anti-regucalcin monoclonal antibody (50-200 ng/ml). The present study suggests that regucalcin plays a role in the regulation of protein kinase activity in the nuclei of proliferative liver cells. J. Cell. Biochem. 71:569-576, 1998. © 1998 Wiley-Liss, Inc.
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  • 325
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    Journal of Cellular Biochemistry 72 (1998), S. iv 
    ISSN: 0730-2312
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: No abstract.
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  • 326
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    Journal of Cellular Biochemistry 71 (1998), S. 577-583 
    ISSN: 0730-2312
    Keywords: hsp70 ; translation ; heat shock proteins ; stress response ; restimulation ; feedback inhibition ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: To develop an alternative to hyperthermia for the induction of hsp70 for presurgical cytoprotection, we investigated the optimal exposure conditions for magnetic field induction of hsp70. Normal human breast cells (HTB124) were exposed to 60-Hz magnetic fields and hsp70 levels were measured following three different exposure conditions: continuous exposure up to 3 h, a single 20-min exposure, and a single 20-min exposure followed by repeated 20-min exposures at different field strengths. In cells exposed continuously for 3 h, hsp70 levels peaked (46%) within 20 min and returned to control levels by 2 h. Following a single 20-min exposure, the return of hsp70 levels to control values extended to more than 3 h. When cells underwent a 20-min exposure followed by repeated 20-min exposures (restimulation) with different field strengths, additional increases in hsp70 levels were induced: 31% at 1 h, 41% at 2 h, and 30% at 3 h. J. Cell. Biochem. 71:577-583, 1998. © 1998 Wiley-Liss, Inc.
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  • 327
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    Journal of Cellular Biochemistry 72 (1998), S. 1-7 
    ISSN: 0730-2312
    Keywords: S phase ; DNA replication ; gene replication ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Events in the S phase of the cell cycle have been investigated to a relatively limited extent in comparison with those in G1 and M phases. Four aspects of S are briefly discussed in this report: (1) the final biochemical step permitting initiation of DNA synthesis, (2) determination of replication timing of individual genes and its mechanism, (3) S phase processes that lead to the onset of M phase, and (4) resetting the S-phase machinery. J. Cell. Biochem. Suppls. 30/31:1-7, 1998. © 1999 Wiley-Liss, Inc.
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  • 328
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    Journal of Cellular Biochemistry 72 (1998), S. 18-29 
    ISSN: 0730-2312
    Keywords: mammalian DNA replication fork ; DNA synthesome ; PCNA ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: The process of DNA replication in mammalian cells is highly complex and has several unique features that distinguish it from simpler prokaryotic systems. The study of mammalian DNA replication lagged behind that of prokaryotes for many years. This was because of the lack of a reliable and efficient mammalian cell-based in vitro DNA replication system. In 1984, the first mammalian-based DNA replication system that initiated DNA synthesis successfully in vitro was developed. The employment of the mammalian in vitro DNA replication system has led to the identification of several DNA replication proteins. This article describes the current knowledge regarding the proteins mediating mammalian DNA replication, as well as how they are proposed to function during DNA synthesis. There is also a discussion of the role the mammalian cell nuclear architecture plays in DNA replication. The evidence for the existence of an organized DNA replication machine in mammalian cells is also presented. J. Cell. Biochem. Suppls. 30/31:18-29, 1998. © 1998 Wiley-Liss, Inc.
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  • 329
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    Journal of Cellular Biochemistry 72 (1998), S. 8-17 
    ISSN: 0730-2312
    Keywords: eukaryote ; DNA replication ; replication origin ; pre-replication complex ; initiation proteins ; origin recognition complex ; DNA unwinding ; nuclear structure ; chromatin structure ; DNA methylation ; animal development ; metazoa ; mammal ; frog ; fly ; yeast ; Xenopus ; Drosophila ; Sciara ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Our understanding of the process by which eukaryotes regulate initiation of DNA replication has made remarkable advances in the past few years, thanks in large part to the explosion of genetic and biochemical information on the budding yeast, Saccharomyces cerevisiae. At least three major concepts have emerged: 1) The sequence of molecular events that determines when replication begins and how frequently each replication site is used are conserved among most, if not all, eukaryotes; 2) specific replication origins are used in most, if not all, eukaryotes that consist of a flexible modular anatomy; and 3) epigenetic factors such as chromatin structure and nuclear organization determine which of many potential replication origins are used at different stages in animal development. Thus, the current state of our knowledge suggests a simple unifying concept - all eukaryotes utilize the same basic proteins and DNA sequences to initiate replication, but the metazoa can change both the number and locations of replication origins in response to the demands of animal development. J. Cell. Biochem. Suppls. 30/31:8-17, 1998.
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  • 330
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    Journal of Cellular Biochemistry 72 (1998), S. 30-36 
    ISSN: 0730-2312
    Keywords: tumor suppressor family ; regulatory mechanisms ; retinoblastoma ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: The intense investigation of the retinoblastoma “tumor suppressor family” members, pRb, pRb2/p130, and p107, has revealed impressive mechanisms evolved to safeguard development and homeostasis in higher eukaryotes. Members of the retinoblastoma family are involved in implementing and controlling three major aspects of cellular life: (1) proliferative growth, (2) differentiation, and (3) apoptosis. The activities of these proteins are highly regulated, enabling them to precisely establish control. The pRb protein is well understood in its regulatory abilities and is considered a classical tumor suppressor. The role of pRb2/p130 protein in growth suppression and its potential as a tumor suppressor have been established during the last few years. The p107 protein, structurally and functionally similar to, but yet distinctive from, pRb2/p130, is characterized at a more rudimentary level. In this report, we review the latest data on the retinoblastoma protein family and its web of regulatory mechanisms. J. Cell. Biochem. Suppls. 30/31:30-36, 1998. © 1998 Wiley-Liss, Inc.
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  • 331
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    Journal of Cellular Biochemistry 72 (1998), S. 37-42 
    ISSN: 0730-2312
    Keywords: cyclin-dependent kinases ; cell growth ; genomic stability ; restriction point control ; tumorigenesis ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: No abstract.
    Additional Material: 1 Ill.
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  • 332
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    Journal of Cellular Biochemistry 72 (1998), S. 50-54 
    ISSN: 0730-2312
    Keywords: p53 ; cell cycle regulation ; p21 ; wip21 ; cancer ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: No abstract.
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  • 333
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    Journal of Cellular Biochemistry 72 (1998), S. 43-49 
    ISSN: 0730-2312
    Keywords: tumor suppression ; p53 ; angiogenesis ; signal transduction ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Tumor suppressors act along diverse biochemical pathways to function as safeguards against cancer. This review summarizes how these pathways can be regulated, primarily by focusing on the well-characterized wild-type p53 tumor suppressor as a paradigm. Specifically, we discuss recent data linking p53 to the processes of signal transduction and angiogenesis. J. Cell. Biochem. Suppls. 30/31:43-49, 1998 © 1998 Wiley-Liss, Inc.
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  • 334
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    Journal of Cellular Biochemistry 72 (1998), S. 55-61 
    ISSN: 0730-2312
    Keywords: osteoblasts ; osteoclasts ; osteoporosis ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Bone is subject to continuous breakdown (resorption) by osteoclasts and rebuilding (formation) by osteoblasts in order to fulfill its functions. Most bone diseases including osteoporosis are due to excessive bone resorption relative to formation. Recent research has generated new insights into the regulation of osteoclast and osteoblast differentiation and function and the interaction between the two cell types. There is increased awareness of the role of mechanical stimuli in bone homeostasis and by inference the function of bone cells. This information can lead to new therapeutic modalities for maintaining a healthy skeleton into old age. J. Cell. Biochem. Suppls. 30/31:55-61, 1998. © 1998 Wiley-Liss, Inc.
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  • 335
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    Journal of Cellular Biochemistry 72 (1998), S. 62-72 
    ISSN: 0730-2312
    Keywords: osteocalcin gene ; osteoblast growth ; osteoblast differentiation ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: The bone tissue-specific osteocalcin gene remains one of a few genes that exhibits osteoblast-restricted expression. Over the last decade, characterization of the promoter regulatory elements and complexes of factors that control suppression of the osteocalcin gene in osteoprogenitor cells and transactivation in mature osteoblasts has revealed transcriptional regulatory mechanisms that mediate development of the osteoblast phenotype. In this review, we have focused on emerging concepts related to molecular mechanisms supporting osteoblast growth and differentiation based on the discoveries that the osteocalcin gene is regulated by homeodomain factors, AP-1 related proteins, and the bone restricted Cbfa1/AML3 transcription factor. J. Cell. Biochem. Suppls. 30/31:62-72, 1998. © 1998 Wiley-Liss, Inc.
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  • 336
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    Journal of Cellular Biochemistry 72 (1998), S. 83-91 
    ISSN: 0730-2312
    Keywords: biomineralization ; calcification ; bone ; dentin ; matrix proteins ; matrix vesicles ; collagen ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Biomineralization is the process by which mineral crystals are deposited in an organized fashion in the matrix (either cellular or extracellular) of living organisms. Over the past 25 years, new insights into the mechanisms that control these processes have been obtained, yet questions asked then still persist, especially in terms of vertebrate mineralization. Specifically, there are still debates concerning the chemical nature of the first mineral crystals formed in bone, dentin, and cementum; the factors leading to the initial deposition of these crystals; and the functions of macromolecules found associated with these crystals. In this review, emphasis is placed on the currently accepted answers to these questions, drawing insight from nonvertebrate systems. It is suggested that there are redundant calcification mechanisms and that, by taking advantage of our current knowledge of these mechanisms, opportunities will be provided for therapeutic manipulation of diseases in which biomineralization is impaired. J. Cell. Biochem. Suppls. 30/31:83-91, 1998. © 1998 Wiley-Liss, Inc.
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  • 337
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    Journal of Cellular Biochemistry 72 (1998), S. 92-102 
    ISSN: 0730-2312
    Keywords: osteopontin ; enhanced cell survival ; inhibition of apoptosis ; bone remodeling ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: The cytokine and cell attachment protein osteopontin (OPN) is not necessary for the development and survival of mice in a clean animal facility. The primary role of OPN appears to be that of facilitating recovery of the organism after injury or infection, which generally causes an increase in its expression. It also is essential for some forms of bone remodeling. OPN stimulates cellular signaling pathways via various receptors found on most cell types and can encourage cell migration. OPN modulates immune and inflammatory responses and possibly negatively regulates Ras signaling pathways. Its apparent ability to enhance cell survival by inhibiting apoptosis may explain why the metastatic proficiency of tumor cells increases with increased OPN expression. J. Cell. Biochem. Suppls. 30/31:92-102, 1998. © 1998 Wiley-Liss, Inc.
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  • 338
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    Journal of Cellular Biochemistry 71 (1998), S. 169-181 
    ISSN: 0730-2312
    Keywords: intermediate filaments ; mitogen-activated protein ; kinase-activated protein kinase-2 ; vimentin ; okadaic acid ; phosphorylation ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Organization of intermediate filament, a major component of cytoskeleton, is regulated by protein phosphorylation/dephosphorylation, which is a dynamic process governed by a balance between the activities of involved protein kinases and phosphatases. Blocking dephosphorylation by protein phosphatase inhibitors such as okadaic acid (OA) leads to an apparent activation of protein kinase(s) and to genuine activation of phosphatase-regulated protein kinase(s). Treatment of 9L rat brain tumor cells with OA results in a drastically increased phosphorylation of vimentin, an intermediate filament protein. In-gel renaturing assays and in vitro kinase assays using vimentin as the exogenous substrate indicate that certain protein kinase(s) is activated in OA-treated cells. With specific protein kinase inhibitors, we show the possible involvement of the cdc2 kinase- and p38 mitogen-activated protein kinase (p38MAPK)-mediated pathways in this process. Subsequent in vitro assays demonstrate that vimentin may serve as an excellent substrate for MAPK-activated protein kinase-2 (MAPKAPK-2), the downstream effector of p38MAPK, and that MAPKAPK-2 is activated with OA treatment. Comparative analysis of tryptic phosphopeptide maps also indicates that corresponding phosphopeptides emerged in vimentin from OA-treated cells and were phosphorylated by MAPKAPK-2. Taken together, the results clearly demonstrate that MAPKAPK-2 may function as a vimentin kinase in vitro and in vivo. These findings shed new light on the possible involvement of the p38MAPK signaling cascade, via MAPKAPK-2, in the maintenance of integrity and possible physiological regulation of intermediate filaments. J. Cell. Biochem. 71:169-181, 1998. © 1998 Wiley-Liss, Inc.
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  • 339
    ISSN: 0730-2312
    Keywords: T-lymphocyte ; apoptosis ; signal transduction ; HgCl2 ; tyrosine phosphorylation ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Exposure to Hg2+ at a wide range of concentrations (approximately 1-100 μM) more or less caused the death of murine thymic T-lymphocytes, and exposure to 1 μM but not 10 μM (or more) of Hg2+ induced DNA fragmentation. Exposure of cells to Hg2+ caused phosphorylation of multiple cellular proteins at the tyrosine residue in a concentration-dependent manner. We found that not only the DNA fragmentation induced by 1 μM Hg2+ but also the cell death bypassing DNA fragmentation caused by 10 μM or more Hg2+ was partly inhibited by protein kinase inhibitors such as staurosporine and herbimycin A. This result suggested the involvement of a protein phosphorylation-linked signal in the mechanism of the Hg2+-mediated cell death with or without DNA fragmentation. Analysis of proteins by both one- and two-dimensional electrophoresis and immunoblot showed that a 52-kDa Shc protein was heavily phosphorylated by an early signal delivered by a high concentration of Hg2+, which also phosphorylated extracellular signal-regulated kinase 1 (ERK1; p44) and ERK2 (p42) of the mitogen-activated protein kinase (MAPK) family in a concentration- and time-dependent manner. The c-Jun amino terminal kinase (p54), which is a distant relative of the MAPK family, was also phosphorylated by the treatment with Hg2+. This eventually formed the signaling cascade that ended with a nuclear target by phosphorylating c-jun at the serine 73. This phosphorylation of c-jun was inhibited by staurosporine. These results suggest that a high level of Hg2+-mediated protein phosphorylation-linked signal induces rapid cell death bypassing DNA fragmentation, whereas a lower level induces cell death accompanying DNA fragmentation. This conclusion in turn implies that DNA fragmentation is not always a prerequisite for the signal transduction-dependent cell death of T-lymphocytes. J. Cell. Biochem. 71:243-253, 1998. © 1998 Wiley-Liss, Inc.
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  • 340
    ISSN: 0730-2312
    Keywords: apoptosis ; necrosis ; phospholipases ; tumor necrosis factor ; Fas ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Phospholipases generate important secondary messengers in several cellular processes, including cell death. Tumor necrosis factor (TNF) can induce two distinct modes of cell death, viz. necrosis and apoptosis. Here we demonstrate that phospholipase D (PLD) and cytosolic phospholipase A2 (cPLA2) are differentially activated during TNF-induced necrosis or apoptosis. Moreover, a comparative study using TNF and anti-Fas antibodies as cell death stimuli showed that PLD and cPLA2 are specifically activated by TNF. These results indicate that both the mode of cell death and the type of death stimulus determine the potential role of phospholipases as generators of secondary messengers. J. Cell. Biochem. 71:392-399, 1998. © 1998 Wiley-Liss, Inc.
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  • 341
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    Journal of Cellular Biochemistry 71 (1998), S. 375-381 
    ISSN: 0730-2312
    Keywords: insulin-like growth factor-I ; insulin-like growth factor binding protein-5 ; smooth muscle cells ; atherosclerosis ; substratum ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Insulin-like growth factor binding protein-5 (IGFBP-5) is synthesized and secreted by smooth muscle cells (SMC). IGFBP-5 synthesis is stimulated five- to sixfold by IGF-I, and IGFBP-5 has been shown to augment IGF-I-stimulated DNA synthesis in this cell type. The ability of IGFBP-5 to augment the SMC response to IGF-I is dependent upon its binding to extracellular matrix. A highly charged region of IGFBP-5 that contains amino acids in positions 201-218 has been shown to mediate binding of IGFBP-5 to human fibroblast extracellular matrix (ECM), and a synthetic peptide containing this sequence inhibits IGFBP-5 binding to fibroblast ECM. In this study we show that exposure of SMC cultures that are constituitively synthesizing IGFBP-5 to a synthetic peptide (termed peptide A) containing this sequence has no effect on its synthesis but reduces its abundance within the ECM. The addition of increasing concentrations of the peptide to SMC cultures resulted in a concentration-dependent reduction in ECM-associated IGFBP-5. In contrast, a control peptide (peptide B), which contained the region of amino acids in positions 131-141 and had a similar charge-to-mass ratio, caused a minimal decrease in ECM binding. This effect was functionally significant since the addition of 10 μg/ ml of peptide A inhibited the cellular replication response to 10 ng/ ml IGF-I by 51%, and peptide B had no effect. The effects of peptide A were not due to nonspecific cytotoxicity since it had no inhibitory effect on the response of these cells to human serum and was associated with only minimal inhibition of the cellular response to platelet-derived growth factor. The findings suggest that inhibiting IGFBP-5 binding to porcine SMC ECM results in reduced cellular responses to IGF-I. J. Cell. Biochem. 71:375-381, 1998. © 1998 Wiley-Liss, Inc.
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  • 342
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    Biologie in unserer Zeit 28 (1998) 
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  • 343
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    Biologie in unserer Zeit 28 (1998), S. 6-15 
    ISSN: 0045-205X
    Keywords: Life and Medical Sciences
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Wir haben bei wesentlichen Teilen unseres Tuns das Gefühl, daß wir freientscheiden können, das heißt ohne äußeren und inneren Zwang. Die allgemeine überzeugung, daß es sich hierbei nicht um eine Täuschung handelt, ist die Grundlage dafür, daß wir für solche Willenshandlungen zur Verantwortung gezogen werden können. Sie werden uns zugerechnet  -  im Gegensatz zu den Handlungen, bei denen wir als unzurechnungsfäbig gelten. Nach herkömmlicher Meinung geht den Willkür-handlungen ein mentales Ereignis voraus, nämlich ein Willensakt dieser gilt als der Verursacher der Handlung (Abbildung 1). Nach Kant ist der Wille das Vermögen des Menschen, eine Handlungskette von sich aus ohne vorausgehende Fremdverursachung zu beginnen [20]. Dieser philosophischen Auffassung entspricht das alltagspsychologische Verständnis: Ich habe bei Willkürhandlungen das unabweisliche Gefühl, daß ich es bin, der das wollte, was gerade von meinem Körper getan wird, ganz im Gegensatz zu Reflexen oder neurotischen Zwangshandlungen, bei denen die Betroffenen das Gefühl haben, daß sie diese Verhaltensweisen ohne oder gar gegen ihren Willen tun.Die genaue Erforschung von Willenshandlungen durch die Volitionspsychologie (die Psychologie, die sich mit „Volitionen“, Willenshandlungen, beschäftigt) fördert freilich ein viel komplizierteres Bild zutage.
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    Biologie in unserer Zeit 28 (1998), S. 41-41 
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  • 345
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    Biologie in unserer Zeit 28 (1998), S. 44-44 
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    Biologie in unserer Zeit 28 (1998), S. 47-47 
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    Biologie in unserer Zeit 28 (1998), S. 45-48 
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  • 348
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    Biologie in unserer Zeit 28 (1998), S. 50-50 
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  • 349
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    Biologie in unserer Zeit 28 (1998), S. 60-61 
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  • 351
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    Biologie in unserer Zeit 28 (1998), S. 63-63 
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  • 352
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    Biologie in unserer Zeit 28 (1998), S. 62-63 
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    Biologie in unserer Zeit 28 (1998), S. 64-71 
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    Keywords: Life and Medical Sciences
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Viele Erkenntnisse über das Geschehen in einer Zelle vermitteln uns das Bild eines Fließgleichgewichts, das es der Zelle erlaubt, sich flexibel auf änderungen der Umwelt einzustellen. Während dieses Prinzip für Stoffwechselprozesse schon lange akzeptiertes Lehrbuchwissen darstellt, haben Untersuchungen zum Proteinabbau dieses Dogma nun auch auf proteolytische Prozesse erweitert. Die meisten zelluläen Proteine werden ständig neu gebildet und ebenso auch wieder abgebaut. Hierbei können sich ihre individuellen Halbwertszeiten je nach Funktion der Proteine stark voneinander unterscheiden. So besitzen Enzyme, die wichtige metabolische Kontrollfunktionen in der Zelle ausüben, Halbwertszeiten im Bereich von Minuten, während andere Proteine über Monate stabil vorliegen können. Der gezielte Proteinabbau stellt für die Zelle ein wirkungsvolles Kontrollinstrument dar, um die Konzentrationen wichtiger regulatorischer Proteine schnell und irreversibel zu senken. Auf diese Weise kann sich die Zelle zudem von abnormalen, wie zum Beispiel falsch gefalteten oder mutierten, und damit funktionsunfähigen Proteinen befreien, deren Ansammlung sie auf längere Sicht hin schäadigen würde. überdies werden wertvolle Aminosäurebausteine im Sinne eines effektiven Recyclings wieder zur Synthese neuer Proteine eingesetzt. Da die Proteinbiosynthese ein energieaufwendiger Prozeß ist, muß der regulierend eingesetzte Proteinabbau einer strikten Kontrolle unterliegen. Wir beginnen gerade zu verstehen, wie die Zelle das Kunststück fertigbringt, aus der großen Vielzahl aller zelluläen Proteine mit hoher Präzision diejenigen auszuwählen, die zu einem bestimmten Zeitpunkt abgebaut werden sollen.
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  • 354
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    Biologie in unserer Zeit 28 (1998), S. 72-81 
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    Keywords: Life and Medical Sciences
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Vor etwa zwölf Jahren habe ich bereits an gleicher Stelle eine übersicht über Trypanosomen vorgestellt [3] und bemerke nun erstaunt, welche Entwicklung die Forschung in diesem Dezennium genommen hat und welch tiefe Einblicke in die molekulare Organisation und die zellbiologische Funktionsweise dieser Parasiten erzielt wurden, nur: Eine wirksame Kontrolle der Schlafkrankheit oder eine unbedenkliche Behandlungsmethode, die in jedem Fall eingesetzt werden kann und Parasiten aller Stadien ohne Nebenwirkungen climiniert, ist noch immer nicht gefunden. Im Gegenteil, sozialpolitische Umwälzungen, ethnische Rivalitäten und massenhafte Flüchtlingsbewegungen in Zentralafrika haben bedenkliche Auswirkungen auch- und besonders- auf die Infektionserkrankungen. Tatsächlich sind in dieser Region in den letzten Jahren wieder verstäkt lokale Epidemien der Schlafkrankheit beobachtet worden, und die Gefahr verheerender Massenerkrankungen, denen wie um die Jahrhundertwende Millionen von Menschen zum Opfer fallen könnten, ist keinesfalls gebannt. Vor diesem Hintergrund mußman die faszinierenden molekularen Details betrachten, mit denen dieser Parasitseinen überlebenskampf führt und sich gegen die geballte Macht des Immunsystems durchsetzt.In den letzten Jahren wurde aber auch deutlich, daß Trypanosomen im Verlauf der Evolution auf einer sehr frühen Stufe aus der allgemeinen Entwicklung der Eukaryoten ausgeschert sind und somit den Blick auf die Entstehungsgeschichte der Organismen von den Prokaryoten zu den höheren Lebensformen freigeben. Diese Erkenntnis hat die Parasiten zu beliebten Forschungsobjekten gemacht und mittlerweile eine Reihe detailreicher Bilder zellbiologischer Phänomene geliefert, die bis dahin unbekannt waren. Im ersten Teil dieses Aufsatzes wird eine Auswahl interessanter Beispiele aus diesem Bereich veranschaulicht, im zweiten Teil stehen die parasitologischen Probleme im Vordergrund.
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    Biologie in unserer Zeit 28 (1998), S. 107-113 
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    Keywords: Life and Medical Sciences
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Beim Prozeß der Genexpression wird die in Form doppelsträngiger DNA gespeicherte genetische Information durch Transkription und Translation in Proteinsequenzen umgewandelt. Da zu einem gegebenen Zeitpunkt nur eine begrenzte Anzahl von Genprodukten benötigt wird, unterliegt das Abrufen dieser Information auf mehreren Ebenen einer strengen Kontrolle. Hierbei ist die Regulation der Transkriptionsinitation der ökonomischste und deshalb am häufigsten vorkommende Mechanismus, durch den die Aktivität von Genen zeitlich und  -  in mehrzelligen Organismen-auch räumlich kontrolliert wird.In diesem Artikel wird an den Beispielen natürlicher und synthetischer Promotoren aus Escberichia coli erläutert, welchen Einfluß die DNA-Sequenz eines prokaryo tischen Promotors auf sein Funktionsprogramm ausübt und nach welchen Prinzipien dieses Programm wiederum das Aktivierungs- oder Repressionspotential regulatorischer Proteine beeinflußt. Die dabei vorgestellten Ergebnisse führen zu einem überwiegend kinetisch determinierten Modell der Transkriptionskontrolle eines bakteriellen Operons. Da die Kontrolle pro- und eukaryotischer Transkriptionssignale denselben kinetischen und thermodynamischen Gesetzmäßigkeiten unterliegt, kann mit Hilfe prokaryotischer Regulationselemente auch in höheren Eukaryoten die Aktivität eines Promotors schr effizient kontrolliert werden. Die Funktionsfähigkeit eines solchen heterologen Genregulationssystems Iäßt sich am Modell einer transgenen Maus demonstrieren.
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    Biologie in unserer Zeit 28 (1998), S. X 
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    Biologie in unserer Zeit 28 (1998), S. XIII 
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    Biologie in unserer Zeit 28 (1998), S. XVI 
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    Biologie in unserer Zeit 28 (1998), S. XVIII 
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    Biologie in unserer Zeit 28 (1998), S. 137-144 
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    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Planktonorganismen sind häufig sehr klein und leicht. Ihre Sinkgeschwindigkeiten in ruhendem Wasser sind sehr gering, bei mittelgroßen Formen typischerweise wenige Dezimeter, bei sehr kleinen und leichten wenige Zentimeter pro Tag. Das hat weitreichende ökologische Konsequenzen. Wie kommt es aber, daß kleine Plankter so langsam absinken? Einfache geometrische Beziehungen, Gedankenexperimente und Formelbetrachtungen können helfen, dieses hydrobiologisch bedeutsame Phänomen richtig einzuschätzen.
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    Biologie in unserer Zeit 28 (1998), S. 157-165 
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    Topics: Biology
    Notes: Eine Neuauflage des Streits um den von Ernst Haeckel als „biogenetisches Grundgesetz“ bezeichneten Kausalzusammenhang zwischen Phylogenese und Ontogenese erfuhr im letzten Jahr eine bemerkenswerte Beachtung in den Medien. Ernst Haeckel ein Fälscher? Das biogenetische Grundgesetz widerlegt? Ein kurzer Blick zurück in die Geschichte läßt am Sensationswert dieser Meldungen jedoch zweifeln. Denn bereits zu Beginn dieses Jahrhunderts war dieser Streit, geführt mit nahezu denselben Argumenten wie heute, Gegenstand der öffentlichen Diskussion. In den folgenden Beiträgen wird die historische Entwicklung der Auseinandersetzung nachgezeichnet und aktuell bewertet.
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    Biologie in unserer Zeit 28 (1998), S. 165-166 
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    Biologie in unserer Zeit 28 (1998), S. 270-280 
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    Notes: Die alljährlichen Wanderungen von Millionen von Zugvögeln gehören dit zu den faszinierendsten Schauspielen der Natur. Vogelzug ist auf allen Kontinenten zu finden; seine Formen sind vielfältig. In unserer heimischen Vogelwelt reicht dies von Arten, die nicht alljährlich wandern und dann meist nur harschen Wintern ausweichen, wie der Kohlmeise, über solche Arten, die nur relativ kurz ziehen und dennordischen Winter im südlichen Europa verbringen, wie viele Greifvögel, das Rotkehlchen oder der Star, bis zu denen, die regelmäßlig;ig über riesige Distanzen wandern, wie viele der heimischen Grasmücken, die Laubsänger oder der Gartenrotschwanz, die im tropischen Westafrika überwintern. Der Weißlig;storch oder die Rauchschwalbe „Überwintern bis im südlichen Afrika, und die Küstenseeschwalbe pendelt sogar alljährlich zwischen arktischen Brutgebieten und antarktischen „überwinterungsgebieten“, eine Strecke von bis zu 40 000 km jährlich [10].Während bei vielen der Kurz- und Mittelstreckenzieher häufig unmittelbare Witterungsfaktoren den zeitlichen Verlauf des Zuges bestimmen („Winterflucht“), geschieht die Steuerung bei den Fernziehern vornehmlich nach einem angeborenen, also genetisch bestimmten Raum-Zeit-Programm [12]. Der Aufbruch zum Zug, er erfolgt vielfach, wenn die Um weltbedingungen noch komfortabel sind, die Zugweglänge, die Richtungsfindung einschließlig;lich Richtungsänderungen und die Beendigung des Zuges folgen angeborenen Programmen, die über innere Jahreskalender organisiert sind [9, 13]. Zur Orientierung dienen biologische Kompasse, die Sonne, die Gestirne und vor allem das Magnetfeld der Erde [13].
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    Biologie in unserer Zeit 28 (1998), S. 314-321 
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    Topics: Biology
    Notes: Die heilige Lotusblume gilt in den asiatischen Religionen als Symbol der Reinheit: Makellos sauber entfalten sich die Blätter aus dem Schlamm der Gewässer. Dieses Phänomen der Selbstreinigung wurde im Detail untersucht und gewährt erstaunliche Einblicke in die Möglichkeiten der Natur, sich gegen den allgegenwärtigen Schmutz, aber auch gegen Pathogene zu wehren. Es zeigt sich darüber hinaus, daßlig; es möglich ist, künstliche Oberflächen mit vergleichbaren Eigenschaften zu entwickeln, etwa durch die Oberflächenbehandlung von Gebäudefassaden oder Autos, die selbst starkem Regen und Verschmutzungen standhalten oder beides abweisen. Dieses dürfte nur noch ein Frage der Zeit sein.
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    Biologie in unserer Zeit 28 (1998), S. 322-323 
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    Biologie in unserer Zeit 28 (1998), S. 324-330 
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    Biologie in unserer Zeit 28 (1998), S. 330-330 
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    Keywords: Life and Medical Sciences
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  • 368
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    Biologie in unserer Zeit 28 (1998), S. 332-332 
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    Keywords: Life and Medical Sciences
    Source: Wiley InterScience Backfile Collection 1832-2000
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  • 369
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    Biologie in unserer Zeit 28 (1998), S. XIV 
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  • 370
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    Biologie in unserer Zeit 28 (1998), S. XII 
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    Keywords: Life and Medical Sciences
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  • 371
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    Biologie in unserer Zeit 28 (1998), S. 340-340 
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    Keywords: Life and Medical Sciences
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  • 372
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    Biologie in unserer Zeit 28 (1998), S. 348-361 
    ISSN: 0045-205X
    Keywords: Life and Medical Sciences
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Ozon (O3) wird hinsichtlich seiner direkten und indirekten Einwirkung auf Pflanzen diskutiert (Abbildung 1). Die indirekte Einwirkung resultiert aus der seit mehreren Jahren beobachteten Zerstörung der Ozonschicht in der Stratosphäre (Ozonloch). Aufgrund dieses O3-Abbaus gelangt die schädigende UV-B-Strahlung in erhöhtem Maßlig;e zur Erdoberfläche. Direkt als Gas wirkt Ozon in der bodennahen Troposphäre auf Pflanzen ein, hier vor allem aufgrund einer erfolgten O3-Anreicherung. Beide Wirkungspfade werden durch anthropogene Luftverunreinigungen vermittelt. Die folgende Abhandlung betrachtet die Wirkung des troposphärischen Ozons auf Pflanzen.
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  • 373
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    Biologie in unserer Zeit 28 (1998), S. 362-370 
    ISSN: 0045-205X
    Keywords: Life and Medical Sciences
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: ANT XV/3, wie es nüchtern im technischen Sprachgebrauch heißt, ist abgeschlossen. Diese Expedition des Forschungseisbrechers „Polarstern“ (Abbildung 1) begann ann 13. Januar 1998 in Kapstadt (Sädafrika), führte uns in die Packeiszone des sädöstlichen Weddellmeeres im atlantischen Sektor des antarktischen Ringozeans und endete am 26. März in Punta Arenas (Chile). Die einzigartige Tierwelt auf dem bis 500 m tiefen antarktischen Kontinentalsockel ist stellenweise so unglaublich reich an verschiedenen systematischen Gruppen und Lebensformen, daßlig; wir noch während der Expedition beschlossen, einige von uns als besonders interessant empfundene Ergebnisse einem breiten Leserkreis vorzustellen.
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  • 374
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    Biologie in unserer Zeit 28 (1998), S. 386-386 
    ISSN: 0045-205X
    Keywords: Life and Medical Sciences
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Additional Material: 2 Ill.
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  • 375
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    Biologie in unserer Zeit 28 (1998), S. 390-394 
    ISSN: 0045-205X
    Keywords: Life and Medical Sciences
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Neben dem Regenwurm spielen die weißlig;lichen Enchytraciden eine wichtige Rolle in der Bodenbiologie. In Schulwerken werden sie eher am Rande berücksichtigt [3]. Dabei bieten die „Topfwürmer“ für praktische Untersuchungen im Unterricht manche Vorzüge: Ihr durchscheinender Körper erlaubt unter dem Mikroskop direkte Einblicke in Körperbau und -funktionen [8]. Als Versuchstiere sind sie wegen ihrer geringen Groößlig;e sowie ihrer Anspruchslosigkeit einfach zu halten. Ohne nennenswerten Aufwand können Schüler der Mittel- und Oberstufe weitgehend selbständig mit dem kleinen weißlig;en Bruder des prominenten Regenwurms experimentieren.
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  • 376
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    Bioelectromagnetics 19 (1998), S. 75-78 
    ISSN: 0197-8462
    Keywords: electromagnetic fields ; pulsed magnetic fields (PEMFs) ; osteoporosis ; bone density ; microgravity ; Life and Medical Sciences ; Occupational Health and Environmental Toxicology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Physics
    Notes: A 1984 study determined the effect of a 72 Hz pulsating electromagnetic field (PEMF) on bone density of the radii of post-menopausal (osteoporosis-prone) women, during and after treatment of 10 h daily for 12 weeks. Bone mineral densities of the treated radii increased significantly in the immediate area of the field during the exposure period and decreased during the following 36 weeks. Bone density determination of the radii of these women, remeasured after eight years, suggests no long-term changes. The bone density-enhancing effect of PEMFs should be further studied, alone and in combination with exercise and pharmacologic agents such as the bisphosphonates and hormones, as prophylaxis in the osteoporosis-prone postmenopausal woman and as a possible block to the demineralization effect of microgravity. Bioelectromagnetics 19:75-78, 1998. © 1998 Wiley-Liss, Inc.
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  • 377
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    Bioelectromagnetics 19 (1998), S. 79-84 
    ISSN: 0197-8462
    Keywords: memory ; radial arm maze ; rodents ; ELF ; Life and Medical Sciences ; Occupational Health and Environmental Toxicology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Physics
    Notes: A series of four experiments was performed to determine the effect of exposure to a 50 Hz magnetic field on memory-related behaviour of adult, male C57BL/6J mice. Experimental subjects were exposed to a vertical, sinusoidal magnetic field at 0.75 mT (rms), for 45 min immediately before daily testing sessions on a spatial learning task in an eight-arm radial maze. Control subjects were only exposed to a background time-varying field of less than 50 nT and the ambient static field of about 40 μT. In each experiment, exposure significantly reduced the rate of acquisition of the task but did not affect overall accuracy. This finding is consistent with the results of another study that found that prior exposure to 60 Hz magnetic fields affected spatial learning in rats. Bioelectromagnetics 19:79-84, 1998. © 1998 Wiley-Liss, Inc.
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  • 378
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    Bioelectromagnetics 19 (1998), S. 85-91 
    ISSN: 0197-8462
    Keywords: extremely low-frequency electromagnetic fields (ELF-EMF) ; micronucleus formation ; apoptosis ; SCL II cells ; amniotic fluid cells (AFC cells) ; cytogenetic effects ; Life and Medical Sciences ; Occupational Health and Environmental Toxicology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Physics
    Notes: Effects of applying extremely low-frequency electromagnetic fields (ELF-EMF) for different durations (24, 48, and 72 h) and different field intensities (0.1-1.0 mT) on micronucleus (MN) formation and induction of apoptosis were examined in a human squamous cell carcinoma cell line (SCL II) and in a human amniotic fluid cell line (AFC). A statistically significant increase of MN frequency and of induction of apoptosis in SCL II cells after 48-h and 72-h continuous exposure to 50 Hz magnetic field (MF) (0.8 and 1.0 mT) was found. However, exposure of AFC cells to EMF of different intensities and for different exposure times showed no statistically significant differences when compared with controls. These results demonstrate that different human cell types respond differently to EMF. Dose-dependent induction of apoptosis and genotoxic effects, resulting in increased micronucleus formation, could be demonstrated in the transformed cell line, whereas the nontransformed cell line did not show statistically significant effects. These findings suggest that EMF could be a promotor but not an initiator of carcinogenic effects. Bioelectromagnetics 19:85-91, 1998. © 1998 Wiley-Liss, Inc.
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  • 379
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    Bioelectromagnetics 19 (1998), S. 92-97 
    ISSN: 0197-8462
    Keywords: action potentials ; excitable membrane ; postsynaptic potentials ; electronic circuit ; stimulation ; Life and Medical Sciences ; Occupational Health and Environmental Toxicology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Physics
    Notes: Entrainment of output action potentials from repetitively firing pacemaker cells, brought about by regularly spaced excitatory or inhibitory postsynaptic inputs, is a well-known phenomenon. Synchronization of neural firing patterns by extremely low frequency (ELF) external electric fields has also been observed. Whereas current densities of ≈10 A-m-2 are required for direct excitation of otherwise quiescent neural tissue, much lower peak current densities (≈10-2 A-m2) have been reported to entrain spontaneously firing molluscan pacemaker cells. We have developed a neural spike generator circuit model that simulates repetitive spike generation by a space clamped patch (area ≈ 10-7 m2) of excitable membrane subjected to depolarizing current. Picoampere (pA) range variation of DC depolarizing current causes a corresponding smooth variation of neural spike frequency, producing a physiologically realistic stimulus-response (S-R) characteristic. When lower pA range 60 Hz AC current is superposed upon the DC depolarizing current, smooth variation of the S-R characteristic is distorted by subharmonic locking of the spike generator at 30, 20, 15, 12, 10 Hz, and higher order subharmonic frequencies. Although the additional superposition of a physiologically realistic level of “white” current noise, covering the bandwidth 4-200 Hz, suffices to obscure higher order subharmonic locking, locking at 30, 20, and 15 Hz is still clearly evident in the presence of noise. Subharmonic locking is observed at a root mean square AC simulated tissue current density of ≈10-5 A-m-2. Bioelectromagnetics 19:92-97, 1998. © 1998 Wiley-Liss, Inc.
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  • 380
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    Bioelectromagnetics 19 (1998), S. 107-111 
    ISSN: 0197-8462
    Keywords: culture growth cycle ; in vitro cell differentiation ; short- and long-term exposure ; adaptation ; Life and Medical Sciences ; Occupational Health and Environmental Toxicology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Physics
    Notes: The generalized polarization function of the fluorescent probe 2-dimethylamino-6-lauroylnaphthalene has been used to evaluate the lipid dynamics in Friend erythroleukemia cell membrane. The values of this function varied during the culture growth cycle, showing decreased lipid dynamics 24-48 h from the cell seeding. When the cycle occurred in a solenoid producing a magnetic field of 70 μT at 50 Hz in addition to the 45 μT DC of the earth (short-term 4-day exposure), the membrane lipid dynamics during this same time-period decreased by about 10% (P 〈 .04). After long-term (184 days) or extremely long-term (395 days) exposure of the cells to the magnetic field, little additional variation in the membrane lipid dynamics was observed, suggesting an adaptation phenomenon. A variation of membrane lipid dynamics was also observed due to in vitro cell differentiation (P 〈 .02). Nevertheless, the exposure of both undifferentiating and differentiating cells to a highly attenuated magnetic field in a magnetically shielded room (20 nT DC plus 2.5 pT AC) did not induce any modification of membrane lipid dynamics. Bioelectromagnetics 19:107-111, 1998. © 1998 Wiley-Liss, Inc.
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  • 381
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    Bioelectromagnetics 19 (1998), S. 98-106 
    ISSN: 0197-8462
    Keywords: power-frequency ; heart rate variability ; EKG ; HRV ; EMF ; Fourier transform ; Life and Medical Sciences ; Occupational Health and Environmental Toxicology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Physics
    Notes: Heart rate variability (HRV) results from the action of neuronal and cardiovascular reflexes, including those involved in the control of temperature, blood pressure and respiration. Quantitative spectral analyses of alterations in HRV using the digital Fourier transform technique provide useful in vivo indicators of beat-to-beat variations in sympathetic and parasympathetic nerve activity. Recently, decreases in HRV have been shown to have clinical value in the prediction of cardiovascular morbidity and mortality. While previous studies have shown that exposure to power-frequency electric and magnetic fields alters mean heart rate, the studies reported here are the first to examine effects of exposure on HRV. This report describes three double-blind studies involving a total of 77 human volunteers. In the first two studies, nocturnal exposure to an intermittent, circularly polarized magnetic field at 200 mG significantly reduced HRV in the spectral band associated with temperature and blood pressure control mechanisms (P = 0.035 and P = 0.02), and increased variability in the spectral band associated with respiration (P = 0.06 and P = 0.008). In the third study the field was presented continuously rather than intermittently, and no significant effects on HRV were found. The changes seen as a function of intermittent magnetic field exposure are similar, but not identical, to those reported as predictive of cardiovascular morbidity and mortality. Furthermore, the changes resemble those reported during stage II sleep. Further research will be required to determine whether exposure to magnetic fields alters stage II sleep and to define further the anatomical structures where field-related interactions between magnetic fields and human physiology should be sought. Bioelectromagnetics 19: 98-106, 1998. © 1998 Wiley-Liss, Inc.
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  • 382
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    Bioelectromagnetics 19 (1998), S. 112-116 
    ISSN: 0197-8462
    Keywords: combined magnetic fields ; gamma rays ; rat tracheal epithelial cells ; AP-1 ; Life and Medical Sciences ; Occupational Health and Environmental Toxicology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Physics
    Notes: The effect of magnetic fields (50 Hz, 100 μTrms sinusoidal magnetic field combined with a 55 μT geomagnetic-like field) and/or gamma rays of 60 Cobalt on the expression of the c-jun and c-fos proteins was investigated in primary rat tracheal epithelial cells and two related immortalized cell lines. Quite similar patterns and amplitudes of induction of these proteins were evidenced after either ionizing radiation or magnetic field exposure. No synergism after both treatments was observed. These findings suggest that magnetic fields explored in the present study may be considered as an insult at the cellular level. Bioelectromagnetics 19: 112-116, 1998. © 1998 Wiley-Liss, Inc.
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  • 383
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    Bioelectromagnetics 19 (1998), S. 117-122 
    ISSN: 0197-8462
    Keywords: 60 Hz ; magnetic field ; water-maze ; spatial learning ; memory ; Life and Medical Sciences ; Occupational Health and Environmental Toxicology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Physics
    Notes: Rats were trained in six sessions to locate a submerged platform in a circular water-maze. They were exposed to a 1 mT, 60 Hz magnetic field for one hour in a Helmholtz coil system immediately before each training session. In addition, one hour after the last training session, they were tested in a probe trial during which the platform was removed and the time spent in the quadrant of the maze in which the platform was located during the training sessions was scored. Control animals were sham-exposed using the exposure system operating with the coils activated in an anti-parallel direction to cancel the fields. A group of “non-exposed” control animals was also included in the study. There was no significant difference between the magnetic field-exposed and control animals in learning to locate the platform. However, swim speed of the magnetic field-exposed rats was significantly slower than that of the controls. During the probe trial, magnetic field-exposed animals spent significantly less time in the quadrant that contained the platform, and their swim patterns were different from those of the controls. These results indicate that magnetic field exposure causes a deficit in spatial “reference” memory in the rat. Rats subjected to magnetic field exposure probably used a different behavioral strategy in learning the maze. Bioelectromagnetics 19: 117-122, 1998. © 1998 Wiley-Liss, Inc.
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  • 384
    ISSN: 0197-8462
    Keywords: UWB ; recombination ; mutagenesis ; yeast ; ultraviolet light ; Life and Medical Sciences ; Occupational Health and Environmental Toxicology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Physics
    Notes: Cell samples of the yeast Saccharomyces cerevisiae were exposed to 100 J/m2 of 254 nm ultraviolet (UV) radiation followed by a 30 min treatment with ultra-wide band (UWB) electromagnetic pulses. The UWB pulses (101-104 kV/m, 1.0 ns width, 165 ps rise time) were applied at the repetition rates of 0 Hz (sham), 16 Hz, or 600 Hz. The effect of exposures was evaluated from the colony-forming ability of the cells on complete and selective media and the number of aberrant colonies. The experiments established no effect of UWB exposure on the UV-induced reciprocal and non-reciprocal recombination, mutagenesis, or cell survival. Bioelectromagnetics 19: 128-130, 1998. © 1998 Wiley-Liss, Inc.
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  • 385
    ISSN: 0197-8462
    Keywords: melatonin ; magnetic fields ; rat ; single cells ; gland dissociation ; Life and Medical Sciences ; Occupational Health and Environmental Toxicology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Physics
    Notes: The objective of this study was to develop a model for testing various hypotheses concerning possible mechanisms whereby electromagnetic fields might induce suppression of nighttime melatonin production in rodents. A published method for digesting freshly obtained pineal glands to the single cell level was modified, yielding better than 95% viability. An in vitro exposure facility developed for the Food and Drug Administration was used for 12-h overnight exposures of primary pinealocyte cultures to 0.05 mT, 60 Hz, vertical AC and 0.06 μT, DC fields. After exposure, cells were separated from the supernatant by centrifugation. Supernatant melatonin was measured by ELISA assays. Data from 10 experiments demonstrated an average 46% reduction in norepinephrine-induced production of melatonin in the pinealocytes. The results support the hypothesis that EM exposure can produce pineal gland melatonin suppression by affecting individual cells. Bioelectromagnetics 19:123-127, 1998. Published 1998 Wiley-Liss, Inc.
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  • 386
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    Biologie in unserer Zeit 28 (1998), S. 166-167 
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    Keywords: Life and Medical Sciences
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  • 387
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    Biologie in unserer Zeit 28 (1998), S. 186-186 
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    Keywords: Life and Medical Sciences
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  • 388
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    Biologie in unserer Zeit 28 (1998), S. 169-180 
    ISSN: 0045-205X
    Keywords: Life and Medical Sciences
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Die belebte Welt hat über Millionen von Jahren raffinierte biomolekulare Funktionssysteme geschaffen, die es dem Organismus gestatten, auf kleinste Veranderungen in der jeweiligen Umgebung empfindlich zu reagieren. Rezeptoren, die wie Antennen den Kontakt zwischen der Zelle und der Umgebung herstellen, erlauben es, ein bestimmtes Zielmolekül neben Tausenden von anderen Molekülen zu erkennen. Dabei werden unzählige biochemische Reaktionen in Gang gesetzt, die es dem Organismus ermöglichen, das Signal urn ein Vielfaches zu verstärken und ganz gezielt darauf zu antworten. So liegt esnahe, diese ausgeklügelten Mechanismen der Erkennung und Umwandlung zu nut-Zen, um analytische Fragestellungen zu lösen. Dies geschieht heute in einer Vielzahl von unterschiedlichen Varianten auf dem Gebiet der Analytischen Biochemie. Als besonders reizvoll und zukunftsweisend sind dabei Entwicklungen auf dem Gebiet der Biosensorik zu betrachten. Durch Kombination der spezifischen biomolekularen Erkennungssysteme mit den relativ unspezifischen, aber sehr empfindlich messenden und miniaturisierbaren Sensoren sind neue Analyseverfahren in Sicht. Die Fortschritte, die zur Zeit auf den Gebieten der Biotechnologie und der Mikroelektronik gemacht werden, lassen in Zukunft auf einen breiten Einsatz der Biosensoren hoffen.
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    Biologie in unserer Zeit 28 (1998), S. 192-192 
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    Keywords: Life and Medical Sciences
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    Biologie in unserer Zeit 28 (1998), S. 201-213 
    ISSN: 0045-205X
    Keywords: Life and Medical Sciences
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Die Aufgabe jeder Pflanzenzüchtung besteht darin, Pflanzen weiter zu entwickeln, die den ständig wachsenden Bedürfnissen der Gesellschaft entsprechen. Im Gegensatz zur Landwirtschaft ist in der Forstpflanzenzüchtung wegen der langen Nutzungs- und Reproduktionszeiträume von Bäumen eine nennenswerte Selektion hinsichtlich forstwirtschaftlich bedeutender Merkmale nur in sehr begrenztem Umfang möglich. Dennoch erscheint auch bei langlebigen Bäumen eine Anwendung gentechnischer Methoden sinnvoll, wobei die Erarbeitung des Gentransfers nicht nur aus züchterischen Gründen nötig, sondern auch für die biologische Grundlagenforschung bedeutsam ist.
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    Biologie in unserer Zeit 28 (1998), S. 223-223 
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    Keywords: Life and Medical Sciences
    Source: Wiley InterScience Backfile Collection 1832-2000
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  • 392
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    Biologie in unserer Zeit 28 (1998), S. 226-226 
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    Keywords: Life and Medical Sciences
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  • 393
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    Biologie in unserer Zeit 28 (1998), S. 259-259 
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    Keywords: Life and Medical Sciences
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
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  • 394
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    Biologie in unserer Zeit 28 (1998), S. 241-245 
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    Keywords: Life and Medical Sciences
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Die Raffinesse, mit der carnivore Pflanzen Beute fangen, verlockt zur Beschäftigung mit diesen Pflanzen. Carnivore Pflanzen sind autotroph und können daher auch ohne tierische „Kost“ wachsen. Selektionsvorteile könnten sich aber bei der Besiedlung nährstoffarmer Standorte ergeben. Die Fangorgane selbst sind mehr oder minder metamorphosierte Blätter. Die Beute, häufig flinke Insekten, muß gefangen und festgehalten werden. Außerdem müssen Verdauungsenzyme nach außen abgegeben werden, um die Beutetiere zu zersetzen, deren Bausteine von der Pflanze aufgenommen und verwendet werden. Die Abgabe proteolytischer Enzyme ist bei den carnivoren Pflanzen besonders ausgeprägt und bekannt, aber auch keimende Samen, Pilze und Bakterien sezernieren sie. Das hier beschriebene Experiment zum Nachweis proteolytischer Enzyme ist sehr einfach, man verwendet Filmstücke, die normalerweise als Abfall weggeworfen werden.
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  • 395
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    Biologie in unserer Zeit 28 (1998), S. 268-268 
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    Keywords: Life and Medical Sciences
    Source: Wiley InterScience Backfile Collection 1832-2000
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  • 396
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    Biologie in unserer Zeit 28 (1998), S. 281-293 
    ISSN: 0045-205X
    Keywords: Life and Medical Sciences
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Essentielle Aminosäuren sind Eiweißlig;bausteine, die der menschliche und tierische Stoffwechsel selbst nicht bereitstellen kann. Sie müssen mit der Nahrung aufgenommen werden. Der Bedarf wächst überdurchschnittlich mit den steigenden Ernährungsansprüchen der Weltbevölkerung, die in nur zwölf Jahren von jetzt sechs auf sieben Milliarden Menschen im Jahr 2010 zunehmen wird. Kann der Bedarf von der Agrarwirtschaft oder durch fermentative Herstellung und chemische Synthese gedeckt werden?
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 397
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Biologie in unserer Zeit 28 (1998), S. XV 
    ISSN: 0045-205X
    Keywords: Life and Medical Sciences
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Type of Medium: Electronic Resource
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  • 398
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Biologie in unserer Zeit 28 (1998), S. 371-380 
    ISSN: 0045-205X
    Keywords: Life and Medical Sciences
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Die Entwicklung der heute in der Landwirtschaft und im Gartenbau genutzten Kulturpflanzen ist eine der wichtigsten Leistungen in der Geschichte der Menschheit. Züchterische Maßlig;nahmen des Menschen haben zum Ziel, Pflanzen so zu verändern, daßlig; sie besser an seine Bedürfnisse angepaßlig;t sind. Die Eingriffe durch Züchtung nennt man „gelenkte Evolution“. Ausgehend von wild vorkommenden Arten hat der Mensch Nutzpflanzen geschaffen, die ohne seine Hilfe in der freien Natur auf Dauer nur geringe überlebenschancen hätten. Neben den Nutzpflanzen findet man in der Natur noch viele wilde Arten, die mit den Kulturpflanzen verwandt sind und sich häufig mit ihnen kreuzen lassen. Die wilden Arten verfügen über ein genetisches Potential, auf das in den letzten Jahren immer häufiger zurückgegriffen worden ist, um Zuchtziele des Menschen zu verwirklichen. Vor allem müssen ständig neue Resistenzen gegen Krankheiten und Schädlinge gefunden werden, um dem Infektionsdruck der Krankheitserreger zu widerstehen. Aber auch Gene für Toleranz gegenüber abiotischem Streßlig;, wie Kälte, Dürre, Salz oder Aluminiumtoxizität, sind in den Wildarten vorhanden. Sie können in die Kulturpflanzen eingekreuzt werden, um sie gegen diese Streßlig;faktoren widerstandsfähiger zu machen.Voraussetzung für den Gentransfer von einer Wildart in eine Kulturart ist ihre Kreuzbarkeit. Darüber hinaus mußlig; im Kreuzungsbastard crossing over zwischen homologen Chromosomen gewährleistet sein. Wenn die Chromosomen nicht zu natürlichem crossing over in der Lage sind, können genetische Paarungsmechanismen in der Meiose eingesetzt werden, die zu dem gewünschten Gentransfer führen.Im folgenden soll anhand von drei Beispielen die Bedeutung des genetischen Potentials wilder und verwandter Pflanzenarten für die Verbesserung der Krankheitsresistenz und Inhaltsstoffe sowie Toleranz gegen abiotischen Streßlig; bei Kulturpflanzen demonstriert werden.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 399
    ISSN: 0045-205X
    Keywords: Life and Medical Sciences
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 400
    ISSN: 0045-205X
    Keywords: Life and Medical Sciences
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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