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  • Cell & Developmental Biology  (58)
  • Uterus  (2)
  • Agrobacterium  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Molecular genetics and genomics 209 (1987), S. 580-584 
    ISSN: 1617-4623
    Keywords: Rhizobium ; Agrobacterium ; TDNA ; Insertion sequence
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The DNA sequence from a Rhizobium leguminosarum 300 (RL300) plasmid that contains homology to the Tc-DNA of Agrobacterium tumefaciens is described. The RL300 sequence has 78% homology to a 359 bp sequence in the Tc-DNA of pTi15955. The RL300 homology starts approximately 100 bp from the 24 bp border sequence of the TL-DNA and ends approximately 3 bp from an IS66 homolog in the Tc-DNA. An unusual feature of the RL300 homology is the presence of 81 bp direct repeats with Tc-DNA homology, separated by 201 bp. One end of each direct repeat has a 12 bp palindrome. Four cloned sequences of RL300 with homology to the T DNA region were hybridized to plasmid lysates of RL300 derivatives to determine the source of each plasmid. The sequenced homolog, originally on pRH228, was isolated from pRL7JI; the other 3 homologs were isolated from the transmissable plasmids pRL7JI (pRH235) and pRL8JI (pRH235 and pRH236).
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-0878
    Keywords: Trophoblastic cells ; Spiral artery ; Extracellular matrix ; Uterus ; Macaca fascicularis (Primates) ; Macaca mulatta (Primates)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract The processes by which trophoblast cells invade and modify the walls of the uteroplacental arteries of macaques during the course of gestation were examined. Antibodies to cytokeratins were employed to identify trophoblast, anti-desmin antibody to identify smooth muscle, and antibodies to type IV collagen, laminin, and fibronectin to examine changes in extracellular matrix distribution in the arterial wall. During early gestation, endovascular trophoblast adhered to the arterial wall, often in an asymmetrical distribution. As trophoblast cells moved outwardly into the tunica media, the basement membrane underlying the endothelium was lost, as indicated by gaps in the layer when stained for type IV collagen and laminin. Trophoblast cells became sequestered in the vessel wall where they hypertrophied and became surrounded by a capsule containing type IV collagen and laminin. As the trophoblast cells became established in the vessel wall, the muscular layer of the artery became discontinuous. Throughout gestation it was common for trophoblast cells to invade the vessel intimal layer and share the lining of the artery with typical endothelial cells. This general disposition of endovascular and intramural trophoblast persisted into late gestation. In addition, and contrary to the results of earlier studies of macaques, we identified trophoblastic invasion and modification of myometrial segments of the uteroplacental arteries in later gestation. We also found evidence of interstitial trophoblast cells among the stromal cells of the endometrium, especially during early gestation.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Cellular Physiology 125 (1985), S. 127-134 
    ISSN: 0021-9541
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Methylcellulose cultures containing mouse marrow cells at low densities and partially purified preparations of erythropoietin and Interleukin-3 were scored after 2 weeks for the presence of macroscopic multilineage colonies (from “primary” CFU-macro GEMM). Whole cultures were then harvested and replated to assess the number of “secondary” CFU-macro GEMM produced, but not detected, during the primary culture period. In such experiments adherent marrow cells yielded significantly higher numbers of secondary CFU-macro GEMM than did either fresh or nonadherent marrow cells. Removal of macroscopic colonies prior to replating showed that most secondary CFU-macro GEMM were not derived from primary CFU-macro GEMM. In vivo studies also revealed a differential effect of adherence separation on the frequency of day 10 CFU-S, which decreased, by comparison to cells capable of long-term repopulation, which increased. Primary adherent CFU-macro GEMM from 5-fluorouracil (5-FU) treated mice showed an 18-fold higher self-renewal capacity than their counterparts in normal marrow. Nevertheless the majority of secondary CFU-macro GEMM obtained from primary cultures of adherent 5-FU cells were again not derived from primary CFU-macro GEMM. Cells capable of immediately generating large multilineage colonies thus appear to represent an intermediate compartment of pluripotent progenitors whose self-renewal properties, may, however, vary over a considerable range. Our results further suggest that these progenitors are derived ultimately from a more primitive adherent cell whose tendency to begin to divide in vitro is low and whose presence correlates with cells capable of long-term myeloid repopulation in vivo.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The placental membranes of the four-eyed opossum were studied by light and electron microscopy. The individual fetuses in each uterus were surrounded by amnion, had allantoic sacs of approximately the same size as each fetus, and were situated in a common yolk sac cavity. The extent of the choriovitelline placenta was marked by a prominent sinus terminalis, and at this margin there was a region where the trophoblast cells penetrated folds of the endometrium. Elsewhere the choriovitelline placenta was closely applied to the uterine epithelium along most of its surface, but the microvilli of the two epithelia did not interdigitate. Numerous inclusion bodies were seen in the trophoblast of both the choriovitelline and bilaminar omphalopleure portions of the placenta, but the aggregates were larger in the latter. The endoderm cells of the choriovitelline placenta had extensive endoplasmic reticulum and numerous mitochondria, but did not have conspicuous absorption canaliculi.Placentation in the four-eyed opossum appears to represent a progressive advance over that of the Virginia opossum both in confluence of the yolk sacs of the fetuses and in having a region of penetration of the maternal endometrium by trophoblast.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The chorioallantoic placenta of the bat (Myotis lucifugus) is hemodichorial and has an ectoplasmic layer and an intrasyncytial lamina interposed between the maternal blood space and the underlying endoplasmic portion of the syncytial trophoblast. The barrier and/or transport function of the trophoblast of this species was investigated. When Thorotrast was injected into the maternal vascular system, only small amounts appeared in the trophoblast, and it could not be demonstrated deep to the syncytial trophoblast.Injected peroxidase and ferritin were both rapidly taken up by the trophoblast, these tracers being found in coated vesicles and tubules, in multivesicular bodies, and in dense bodies. Peroxidase was transported across the trophoblast and could be found in macrophages in the fetal connective tissue and in vesicles in the fetal endothelium. Since ferritin is present in the cytotrophoblast, macrophages and fetal endothelium in uninjected as well as injected animals, the exogenous material could not be followed beyond the syncytium. In addition to demonstrating the cytological pathway by which absorbed proteins cross the trophoblast of the chorioallantoic placenta of the bat, the results of this study suggest that the labyrinth in this species should be considered a possible route for passage of endogenous proteins to the fetus.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 167 (1970), S. 231-251 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Cytological investigation of Hofbauer cells in various stages of gestation reveals that they are similar to normal macrophages except for unusually large cytoplasmic flanges and included vacuoles. The system of vacuoles is apparently the result of macropinocytotic activity. The individual vacuoles undergo asymmetrical collapse in regions adjacent to small juxtavacuolar tubules thought to be derived from the agranular endoplasmic reticulum. In addition, coated micropinocytotic vesicles are common. Hofbauer cells thus appear to be a type of macrophage with an unusual capacity for fluid ingestion. In younger placentas, Hofbauer cells are usually associated with extracellular compartments within the stroma. These compartments are relatively free of collagen fibrils and demonstrable ground substance and are clearly demarcated from the rest of the stroma by processes of fibroblasts. The abundance of these cells in early placentas, their location in the stroma, and evidence of their pinocytotic activity suggest that these cells may play a role in removal of proteins from interstitial fluid. Hofbauer-like cells were also studied in the guinea pig and the little brown bat. Of these two species, the Hofbauer-like cells of the bat more closely resemble human Hofbauer cells in that they show evidence of extensive macropinocytotic activity.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 175 (1973), S. 539-559 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The protein tracers, horseradish peroxidase and ferritin, are demonstrable in the subzonal space of all preimplantation stages within ten minutes when incubated in vivo or in vitro. However, there is very little uptake of these proteins by ova and two-cell stages. By the blastocyst stage there is greatly increased uptake of exogenous protein. The proteins appear in coated micropinocytotic vesicles and tubules, larger vacuoles, and more complex bodies. Blastocysts from the period of lactationally delayed implantation show an even greater amount of uptake, especially in the supranuclear region. Peroxidase reaction product can be demonstrated in the cavity of day 5 blastocysts in 30 minutes, and in the cavity and basal lamina of the blastocysts during delayed implantation in ten minutes. Ferritin was more sparsely distributed, and was not seen in the blastocyst cavity in any of the time periods. Peroxidase is apparently transported via an intracellular pathway, since it is not seen in the elaborate intercellular spaces between trophoblast cells. Acid phosphatase activity is demonstrable in vacuoles, dense bodies and Golgi cisternae in all stages, indicating that the potential for degradation of ooplasm and phagocytized material by a lysosomal system is present in all of the preimplantation stages examined.
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