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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Experimental dermatology 8 (1999), S. 0 
    ISSN: 1600-0625
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Abstract: Type XII and XIV collagens localize near the surface of banded collagen fibrils and most likely work as a molecular bridge between collagen fibrils. We have shown that both collagens can modulate the interactions between collagen fibrils, allowing fibroblasts to act upon the fibrils to vary the deformability. In the present study the effect of the globular domains (collagenase-resistant domains) of type XII and XIV collagens (XII-NC-3 and XIV-NC-3) on the migration of fibroblasts into the reconstituted type I collagen gel was investigated. Cell attachment and proliferation on the collagen gel were unaffected. The migration of fibroblasts into the gel was increased proportionally to the concentration of collagen. We found that XII-NC-3 and XIV-NC-3 domains caused decreases in the numbers of fibroblasts that migrated into the gel. Heat treatment of XII-NC-3 and XIV-NC-3 or the addition of polyclonal antibodies eliminated the suppressive activity on fibroblast migration, showing that the intact conformation of NC-3 domain is important for suppression of migration. The results suggest that both NC-3 domains influence the deformability of type I collagen fibril networks, which may cause the change in fibroblast migration.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Tetrahedron: Asymmetry 3 (1992), S. 1369-1372 
    ISSN: 0957-4166
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Tetrahedron: Asymmetry 3 (1992), S. 1381-1384 
    ISSN: 0957-4166
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1365-2133
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Background  The epidermal basement membrane (BM) plays important roles in adhesion between epidermis and dermis, and in controlling epidermal differentiation. The BM has been reported to be damaged in sun-exposed skin. Although matrix metalloproteinases (MMPs) are believed to be involved in the BM damage, there is no good in vitro model for examining BM damage by MMPs or for exploring methods to protect the BM.Objectives  To examine the involvement of MMPs in BM damage and approaches to protect the BM from such damage by using an in vitro skin-equivalent (SE) model.Method  SE was prepared by culturing human keratinocytes on contracted collagen gel including human fibroblasts. MMP-1, -2, -3 and -9, laminin 5 and type IV and VII collagens were determined by specific sandwich ELISAs, and MMP-2 and MMP-9 were analysed by gelatin zymography. Histological examination of SE was also carried out.Results  Despite production of BM components such as laminin 5 and type IV and VII collagens in SEs, BM was rarely observed at the dermal–epidermal junction. Several MMPs, such as MMP-1, -2, -3 and -9, were observed to be present in conditioned media and some of them were in active forms. Tissue inhibitor of metalloproteinase (TIMP)-2 was not detected, although TIMP-1 was present. Synthetic MMP inhibitors, CGS27023A and MMP-inhibitor I, which inhibit MMP-1, -2, -3 and -9, markedly augmented deposition of laminin 5 and type IV and VII collagens at the dermal–epidermal junction, resulting in the formation of continuous epidermal BM.Conclusions  Our results indicate that MMPs are involved in the degradation of BM in SEs, and that MMP inhibitors exert a protective effect against BM damage.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 61 (1987), S. 3158-3160 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Nonstoichiometric FexO1−x and FexMyO1−x−y films, where M is either a nonmagnetic element, e.g., Si, or a magnetic element, e.g., Co, were prepared by sputter deposition. They showed increasing ferromagnetic magnetization with decreasing oxygen concentration below 1−x−y〈0.5, and strong perpendicular magnetic anisotropy which overwhelmed the shape anisotropy of the thin ferromagnetic films in certain composition ranges. The magnetization of perpendicular magnetic films attained more than 500 emu/cm3 with an anisotropy energy of 2×106 erg/cm3. Ferromagnetic amorphous metallic phases precipitated between columnar structure of nonmagnetic oxide phase were considered to be responsible for the ferromagnetism of these films. The perpendicular anisotropy was also interpreted by the internal shape effect arising from fine elongated ferromagnetic phases distributed in a nonmagnetic phase with their long axis perpendicular to the film plane. They had an appropriate coercivity for the perpendicular magnetic recording media with a high resistance against wear and corrosion and a low friction constant.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Ltd
    British journal of dermatology 151 (2004), S. 0 
    ISSN: 1365-2133
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Background  Laminin 5 is known to induce the adhesion, spreading and migration of human keratinocytes. In skin wound healing, laminin 5 deposition beneath migrating keratinocytes occurs early and is followed by the formation of hemidesmosomes and then basement membrane.Objectives  To identify factors that regulate the synthesis and secretion of laminin 5 by human keratinocytes during acute wound healing.Methods  Laminin 5 synthesis by human keratinocytes was determined by a specific sandwich enzyme-linked immunosorbent assay. To determine the total amount of laminin 5 synthesized, laminin 5 deposited on culture dishes and inside cells was solubilized by detergent solution and determined separately from conditioned medium, and the total laminin 5 synthesis was calculated. A quantitative polymerase chain reaction method was used to measure the expression levels of laminin 5 genes, LAMA3, LAMB3 and LAMC2, which correspond to the α3, β3 and γ2 chains of laminin 5. We also examined the effects of lysophospholipids, proinflammatory cytokines and growth factors, which are components in acute wound fluids, on laminin 5 synthesis in keratinocytes.Results  Human acute wound fluid at days 1, 2 and 3 stimulated laminin 5 synthesis in cultured human keratinocytes in a concentration-dependent manner, although findings are restricted to one case. Human serum also increased laminin 5 production by human keratinocytes as strongly as the wound fluid did, suggesting that the major active components in acute wound fluid may be derived from those in human serum. Lysophospholipids such as lysophosphatidic acid (LPA), lysophosphatidylcholines (LPCs) and sphingosine-1-phosphate (S1P) increased laminin 5 synthesis in a concentration-dependent manner. Among growth factors, epidermal growth factor, insulin-like growth factor-1, interferon-γ and keratinocyte growth factor increased laminin 5 production in keratinocytes, while platelet-derived growth factor, hepatocyte growth factor and basic fibroblast growth factor were ineffective. Although interleukin-1α had no effect, transforming growth factor (TGF)-α, tumour necrosis factor (TNF)-α and TGF-β1 also stimulated laminin 5 synthesis, and TGF-α and TGF-β1 showed a synergistic effect. Neutralizing antibodies to TGF-α and TGF-β1 markedly inhibited the enhanced laminin 5 synthesis by human serum, suggesting that TGF-α and TGF-β1 are important components to increase laminin 5 in human serum. In line with the increase of laminin 5 synthesis, the expression levels of all three laminin 5 genes were also augmented by TGF-α and TGF-β1.Conclusions  Laminin 5 synthesis in human keratinocytes was augmented by inflammatory cytokines and growth factors such as TGF-α, TGF-β1 and TNF-α, and lysophospholipids such as S1P, LPA and LPCs, which are supposed to be present in acute wound fluid. The increased laminin 5 protein in the wound area presumably enhances wound repair by stimulating adhesion and migration of keratinocytes on the wound bed and by facilitating basement membrane formation at the dermal–epidermal junction.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Journal of Magnetism and Magnetic Materials 104-107 (1992), S. 781-782 
    ISSN: 0304-8853
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Physics
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Journal of Magnetism and Magnetic Materials 104-107 (1992), S. 781-782 
    ISSN: 0304-8853
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Physics
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Applied Surface Science 60-61 (1992), S. 39-44 
    ISSN: 0169-4332
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Physics
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 1437-7772
    Keywords: Key words Rectal cancer ; Poorly differentiated adenocarcinoma ; Multidisciplinary treatment ; Radiotherapy ; Tegafur suppository ; OK-432
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract We administered multidisciplinary treatment to a 37-year-old man with poorly differentiated adenocarcinoma of the rectum which exhibited a fistula between the rectum and the urinary bladder; the tumor was considered unresectable because of extensive local spread at initial evaluation, including a laparotomy. The patient received radiotherapy, consisting of a total dose of 50 Gy, given as fractions of 2 Gy per day 4 days a week. Concurrently with the radiation, the patient also received twice daily a tegafur [1-(2-tetrahydrofuryl)-5-fluorouracil] suppository (750 mg) and 5-fluorouracil ointment (2.5 g) applied to the perianal involved skin lesion. In addition, 5 KE of OK-432 was injected into the tumor nine times during the course of radiation. Because the tumor responded well to this radio-chemo-immunotherapy, the patient was discharged, and was treated only with tegafur suppositories for almost 3 years on an outpatient basis (total dose of tegafur, approximately 1500 g). As a result of the combined therapy, the tumor completely disappeared, while only the recto-urinary fistula remained. The patient has survived without recurrence for 50 months after his initial presentation, and his levels of carcinoembryonic antigen and immunosuppressive acidic protein have decreased from pretreatment values of 85 ng/ml and 1220 μg/ml, respectively, to 0.8 ng/ml and 459 μg/ml, respectively. Although this is only one case, it shows that appropriate multidisciplinary treatment may achieve excellent results even in patients with unresectable poorly differentiated adenocarcinomas of the rectum.
    Type of Medium: Electronic Resource
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