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  • 1975-1979  (7)
  • 1970-1974  (12)
  • Life and Medical Sciences  (19)
  • 11
    ISSN: 0002-9106
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Previous experiments have suggested that the guinea pig chorio-allantoic placenta is a barrier to the maternal-fetal passage of proteins. The means by which the placenta exercises this barrier function were investigated by electron microscopy after injection of peroxidase, ferritin, and Thorotrast. Uptake of protein was by coated vesicles which formed at the trophoblast surface, pinched off, and migrated deeper into the cytoplasm. Some vesicles emptied into multivesicular bodies; others migrated across the trophoblast, emptying their content into the underlying compartment. Peroxidase and ferritin were observed in basement membranes within 10-20 minutes after injection. At longer intervals, the proteins were increasingly difficult to demonstrate in basement membranes, although increased amounts were present in the trophoblast. Neither the basement membranes nor the fetal capillary endothelium constituted an effective barrier to proteins which crossed the trophoblast. The results suggest that the trophoblast is the major barrier to maternal-fetal protein transfer across the labyrinth. The trophoblast appears to exercise this barrier function by (a) having a low rate of protein absorption and (b) having multivesicular bodies and lysosomes which sequester and possibly degrade absorbed proteins. However, the trophoblast is not a complete barrier to the passage of these exogenous proteins which may indicate a normal, albeit minor, pathway of maternal-fetal protein transport.
    Type of Medium: Electronic Resource
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  • 12
    ISSN: 0002-9106
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: With both scanning and transmission electron microscopy, large ectoplasmic projections are found intruding into the lumen from the epithelial cells of the rat uterus. These projections, which are abundant both prior to implantation and during delayed implantation, communicate with the underlying cytoplasm only by a small pedicel as though in the process of pinching off. However, introduction of tracer material into the uterine lumen demonstrates the pinocytotic nature of these projections. Within three minutes after introduction of tracer the projections, termed pinopods, contain numerous vacuoles filled with tracer. Within ten minutes large vacuoles containing tracer are present in the apical cytoplasm subjacent to the individual pinopods.The varied images observed in the experimental and control materials suggest that there is a continual turnover of pinopods. Initially a simple ectoplasmic projection, the pinopod apparently develops rapidly into a mass of ectoplasm 2-3 μ in diameter with multiple folds and pockets at its surface and numerous internal vacuoles. Following a period of active endocytosis of fluid, the pinopod becomes more spherical and, together with contained material, is withdrawn into the apical cytoplasm.It is suggested that pinocytosis might play a role in producing apposition of the blastocyst to the luminal epithelium, in passing information from the blastocyst to the stroma, and in diminishing the molecular contents of the uterine lumen during specific times in the reproductive process.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 13
    ISSN: 0002-9106
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The annular hematoma of the shrew, Blarina brevicauda, is a specialized portion of the yolk-sac wall. In this study, we have examined the fine structure of the different cellular components of the annular hematoma. Small pieces of the gestation sacs from seven pregnant shrews were fixed in glutaraldehyde and osmium tetroxide and processed for transmission electron microscopy. In the area of the trophoblastic curtain, the maternal capillary endothelial cells were hypertrophied and syncytial trophoblast surrounded the capillaries. Cellular trophoblast covered part of the luminal surface of the curtain region, whereas masses of apparently degenerating syncytium were present on other areas of the surface. Maternal erythrocytes, released into the uterine lumen from the curtain region, were phagocytized and degraded by the columnar cells of the trophoblastic annulus. No evidence of iron or pigment accumulation was evident in the parietal endodermal cells underlying the annular trophoblast. Parietal endodermal cells were characterized by cuboidal shape, widely dilated intercellular spaces, and cytoplasm containing granular endoplasmic reticulum. Endodermal cells of the visceral yolk-sac accumulated large numbers of electron-dense granules as well as glycogen in their cytoplasm. Hemopoietic areas and vitelline capillaries were found subjacent to the visceral endoderm. The various portions of the yolk-sac wall of Blarina appear to perform complementary functions which are probably important in maternal-fetal iron transfer.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 14
    ISSN: 0002-9106
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The cytological basis for protein transport across the guinea pig visceral yolk sac at 36-44 days of gestation was studied by means of electron microscopy following injection of horseradish peroxidase and ferritin. These results were compared with those obtained after administration of colloidal thorium dioxide. Distribution of the tracer molecules was studied at 2, 10, 20, 40, and 160 minutes after injection into the uterine lumen. All three tracer molecules were rapidly absorbed by endoderm cells. Although most of the protein appeared to be retained in droplets in endoderm cells, some protein was transmitted. Peroxidase was found to be rapidly transmitted across the yolk sac, ferritin somewhat more slowly, and colloidal thorium was not transmitted at all. Protein which had exited from the endoderm cells followed any of three pathways: (1) it crossed the visceral basement membrane and entered the vitelline capillaries; (2) it crossed the mesodermal compartment, crossed the mesothelial cells and entered the exocoelomic cavity; or (3) some of the protein was sequestered by macrophages in the splanchnic mesoderm. The pathways observed are consistent with those suggested by previous authors for the passage of maternal antibodies and serum proteins to the guinea pig fetus.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 15
    ISSN: 0002-9106
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The structure of interacting trophoblast and uterine epithelium was studied in 16 rabbits from seven days zero hours to seven days 20 hours post coitus. The most common type of penetration of the uterus by the trophoblast consisted of a peg from a trophoblastic knob that extended to the basal lamina of the uterine luminal epithelium and was bordered by uterine epithelial cells with which it shared junctional complexes. In early implantation sites there was direct evidence of fusion of the syncytial trophoblast with apical ends of individual uterine epithelial cells. Since no evidence of epithelial dissociation or mechanical intrusion of trophoblast between epithelial cells was found, it is suggested that fusion is the normal method of epithelial penetration by the trophoblast in the rabbit. The cytoplasm of the fused uterine cells was apparently converted into syneytium of the trophoblastic knob. Subsequent to formation of the trophoblastic peg, penetration of the basal lamina and of maternal blood vessels occurred, and the attached trophoblastic knobs increased in width. At later stages when symplasma formation by the uterine epithelium was extensive, fusion included trophoblast between knobs. Since the penetration peg is formed by fusion of trophoblast with uterine epithelium, the cell membrane first associated with the maternal connective tissue is of maternal origin. However, new membrane formed after fusion would be expected to have histocompatibility factors from both the trophoblast and the fused maternal epithelial cells.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 16
    ISSN: 0002-9106
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The allantoic placenta of shrews has been classified as hemochorial, endotheliochorial and endothelioendothelial. Recent confusion has centered on the persistence of an intermediate cellular layer within the interhemal membrane and on its identity. Conflicting interpretations assert, (1) that the intermediate layer represents a continuous trophoblastic lamina (endotheliochorial placenta), or (2) that it consists of a discontinuous “maternal symplasma,” the trophoblast having disappeared early in development (endothelioendothelial placenta).Utilizing thin plastic sections for light microscopy and electron microscopy we find that the disputed intermediate layer comprises an exceedingly thin, but continuous layer of syncytiotrophoblast, and that the shrew placenta is indeed endotheliochorial. However, the interhemal membrane displays a most unusual organization. The trophoblast is sieve-like in that it is honeycombed with interstitial (extracellular) spaces which open freely at both its surfaces. Into these channels project numerous processes of the maternal endothelium, and where these contact trophoblast close junctions are often apparent; in rare instances endothelial processes were seen to penetrate to the fetal surface of the trophoblast, but not through its well-defined basal lamina. Maternal endothelium and trophoblast are separated by an irregular space filled with a dense amorphous material, but it lacks fibrillar components normally found in basal membrane. Peculiarities of the hypertrophied maternal endothelium include an abundance of oriented cytoplasmic fibrillar elements, moderate endoplasmic reticulum and ribosomes, and a marked alignment of mitochondria against the basal cell membrane. Hypertrophied fetal mesenchymal cells often intervene between the fetal endothelium and the rest of the interhemal membrane. Seldom does either abut directly against the basal lamina of the trophoblast; they are usually separated from it by a welter of cytoplasmic processes from both elements, which project into the fetal interstitial space. The fetal endothelial cells are somewhat hypertrophied, and their external processes, like those of the mesenchymal cells, often contain glycogen. Peculiarly, the fetal endothelium lacks a basal lamina. The mesenchymal cells display all the usual ultrastructural characteristics of protein synthesizing cells and appear highly active. Functional implications of the organizational peculiarities of the interhemal membrane are discussed.
    Type of Medium: Electronic Resource
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  • 17
    ISSN: 0002-9106
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The yolk sac of the little brown bat is unusual in that during the course of gestation both the inner endodermal cells (bordering the yolk sac cavity) and outer mesothelium (facing the exocelom) form simple columnar epithelia which persist throughout gestation. These endodermal cells develop an extensive system of agranular endoplasmic reticulum, numerous lipid droplets and unusual “giant” mitochondria. During development the Golgi apparatus changes position from the apical to the basal side of the nucleus, reversing the polarity of the cells. In general, the endodermal cells have cytological features suggestive of synthetic or secretory activity. The mesothelial cells develop an extensive “absorptive apparatus” in their apices, while large crystalloid-containing granules become numerous in their basal cytoplasm. The mesothelial cells have large deposits of glycogen, especially during mid-gestation, but few mitochondria and little granular endoplasmic reticulum. Endodermal cells do not absorb exogenous protein (peroxidase) even if it is injected directly into the yolk sac cavity. However, placement of peroxidase either in the exocelom or in the maternal vascular system results in the appearance of this protein in the “absorptive apparatus” of mesothelial cells as well as in macrophages in the stroma of the yolk sac. While evidence of absorption was clear, no direct evidence of transport of tracer to fetal blood vascular system was obtained. It is postulated that a major function of the hypertrophied mesothelial cells during gestation is the absorption of proteins and possibly other substances from the exocelomic fluid. The major function of the hypertrophied endodermal cells may be synthesis and secretion of substances into the fetal circulation.
    Type of Medium: Electronic Resource
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  • 18
    ISSN: 0002-9106
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The structure of the guinea pig visceral yolk sac from 26 days of gestation to term was studied by transmission and scanning electron microscopy. Particular emphasis was placed on the columnar endoderm cells of the villous portion of the yolk sac. The apical cytoplasm of the endoderm cells contained numerous membrane invaginations, endocytic vesicles, dense tubules and large vacuoles which appeared to form an interrelated absorptive system. The saccular invaginations of the apical cell membrane were specialized by the development of both an amorphous extracellular coat and an internal coat. Both the endocytic vesicles and dense tubules were thought to be derived from the saccular invaginations following detachment of the latter from the cell surface  -  the endocytic vesicles forming by fusion of saccules creating progressively larger structures, and the dense apical tubules forming by a process involving fluid loss from the saccules. Large vacuoles were present deeper in the apical cytoplasm; these probably were formed by fusion of smaller vesicles. The supranuclear cytoplasm contained numerous dense droplets and a Golgi zone. The possible relationships of the droplets to the vacuoles was discussed.
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  • 19
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    American Journal of Anatomy 133 (1972), S. 291-315 
    ISSN: 0002-9106
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Implantation in the ferret occurs during the 24 hours between 12 and 13 days post coitus. The thinned zona pellucida is disrupted irregularly along the lateral aspects of implantation chambers. Some of the trophoblastic cells enlarge and develop into plaques of syncytium. Protoplasmic projections from these syncytial plaques intrude between adjacent uterine luminal epithelial cells to which the syncytium is adhering. Interesting ectoplasmic pads from the syncytial trophoblast indent the uterine epithelial cells prior to adhesion, and there are ectoplasmic regions where trophoblast cell membrane is closely applied to uterine cell membranes at all sites of epithelial penetration. Intrusion of trophoblast between uterine luminal epithelial cells is apparently the major mechanism of epithelial penetration in the ferret.
    Type of Medium: Electronic Resource
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