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  • Cell & Developmental Biology  (58)
  • development  (2)
  • 5HTP  (1)
  • 11
    Electronic Resource
    Electronic Resource
    Protein uptake by rat preimplantation stagesThis study was supported by grant HD 04962 from the National Institute of Child Health and Human Development. (1973)
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 175 (1973), S. 539-559 
    Details
    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.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ar.1091750304
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  • 12
    Electronic Resource
    Electronic Resource
    Uptake of exogenous protein by the preimplantation rabbitThis investigation was supported by grant 2 RO1 HD04962 from The National Institute of Child Health and Human Development. (1974)
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 179 (1974), S. 311-330 
    Details
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: A study of the uptake of exogenous proteins, peroxidase, ferritin, and myoglobin by rabbit blastomeres of different developmental stages was undertaken to determine some of the means by which these stages ingest protein. Exposure of embryos in preimplantation stages, ranging from fertilized ovum to late blastocyst, was carried out in vitro with selected in vivo controls. Blastomeres of early cleavage stages up to the morula show little uptake of peroxidase. However, the endocytosis of peroxidase greatly increases with the morula stages and continues at an elevated level through the blastocyst stages. The uptake of the tracer is initially accomplished via micropinocytotic vesicles and tubules and can have several subsequent fates. The tracer can pass into larger vacuoles and be transported into the cavity of the blastocyst, or can pass into multivesicular bodies where it is presumably degraded by the lysosomal system for cellular use. The use of myoglobin at selected blastocyst stages yielded results similar to those obtained with peroxidase. However, the response by the blastomeres to ferritin is different. Endocytosis of ferritin is scant at all preimplantation stages, even though the ferritin has no difficulty reaching the surface of the blastomeres. The experiment with mechanically denuded blastocysts indicated that ferritin did not adsorb to the cell surface.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ar.1091790304
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  • 13
    Electronic Resource
    Electronic Resource
    The implantation chamber, blastocyst and blastocyst imprint of the rat: A scanning electron microscope studyThis study was supported in part by Grant HD-04962 from the National Institute of Child Health and Human Development. Initial acquisition of the scanning electron microscope used was made possible by Health Sciences Advancement Award 5 SO4 RR 06115. (1975)
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 182 (1975), S. 137-149 
    Details
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Splitting the uterus longitudinally through implantation sites makes it possible to obtain access to blastocysts and implantation chambers during stages of implantation of the blastocyst in the rat. On the afternoon of day 5 of pregnancy, blastocysts lie in a shallow antimesometrial depression and tend to fall free of the uterus when the chamber is opened. On day 6, blastocysts are oriented in a mesometrial-antimesometrial plane, occupy a distinct implantation chamber, and tend to adhere to one side or the other of the uterus, leaving an imprint on the contralateral side. After about noon of day 6, some of the blastocysts split in half laterally, and by day 7 all blastocysts which are exposed are split. In addition to demonstrating increased adhesion of blastocyst to uterine epithelium, the procedure clearly shows the progressive elongation of the implantation chamber. The embryonic cell mass is specifically oriented on day 6, and is clasped but not distorted, whereas the abembryonic trophoblast is slightly compressed and indented by the uterine epithelium. The microvilli of the uterine epithelium within the imprint become progressively flattened when compared to the microvilli of the implantation chamber outside of the imprint. The method provides a means of gaining direct access to the surface of uterine epithelium precisely where it has been in association with the blastocyst not only for scanning electron microscopy but also for studies of the properties of the surface constituents.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ar.1091820202
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  • 14
    Electronic Resource
    Electronic Resource
    Differentiation and migration of endoderm in the rat and mouse at implantationThis study was supported by grants HD 04962 and HD 10342 from the National Institue of Child Health and Human Development. (1978)
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 190 (1978), S. 65-77 
    Details
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The initial differentiation of endoderm at the time of onset of implantation, and the subsequent rapid differentiation of visceral and parietal endoderm were studied in the rat and mouse. Transmission electron microscopy illustrates the reorientation and loosening of embryonic cell mass cells during implantation, as well as cytological evidence that endoderm cells have differentiated. Using scanning electron microscopy, parietal endoderm consists of individual stellate cells with numerous peripheral branching filopodia. As these cells migrate abembryonically, the rest of the embryonic cell mass becomes recom-pacted. The visceral endoderm proliferates and forms a columnar epithelium which has the cytological characteristic of an absorptive epithelium and is able to ingest exogenous proteins. Thus, by 24 hours after implantation, the two endo-dermal derivatives have assumed widely diverse shapes and different types of associations and rates of replication, and are probably performing different functions.
    Additional Material: 16 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ar.1091900107
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  • 15
    Electronic Resource
    Electronic Resource
    Surface coats of the mouse blastocyst and uterus during the preimplantation periodSupported by grant 2 R01 HD04962 from the National Institute of Child Health and Human Development. (1974)
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 180 (1974), S. 31-45 
    Details
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: A glycoprotein coat is demonstrable on the free surface of both the blastocyst and uterine luminal epithelium of the mouse on day 4 and day 5 of normal pregnancy, and on day 7 of delayed implantation, using concanavalin A-peroxidase and ruthenium red. The coats are apparently negatively charged, as shown by their binding with colloidal thorium dioxide. The cell coat on uterine epithelium is appreciably thicker than that on the blastocyst. The information currently available is sufficient to suggest that simplistic mechanisms such as change in charge or total thickness cannot be the sole basis of initial adhesion, but that some localized reduction of the uterine surface coat accompanies adhesion. However, considerably more information is necessary concerning the nature of the surface coats before a more comprehensive understanding of the role of adhesion in implantation can be achieved.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ar.1091800105
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  • 16
    Electronic Resource
    Electronic Resource
    Mouse uterine glands during the peri-implantation period II. Autoradiographic studies (1981)
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 199 (1981), S. 109-127 
    Details
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Protein synthesis and secretion in mouse uterine glands during the peri-implantation period were studied, by both light and electron microscopic autoradiography, after the in vivo administration of tritiated leucine (3H-leucine) and proline (3H-proline). Light microscopic autoradiography revealed that the time course of synthesis and secretion of labeled proteins was constant during days four, five, and six of pregnancy. Labeled material could be detected in the glandular lumen by 45 minutes after administration and in higher concentrations by 90 minutes after administration.Analysis of electron microscopic autoradiographs from days five and six of pregnancy showed that high levels of activity were initially present over the rough endoplasmic reticulum and Golgi complexes and subsequently declined at the longer time intervals (45 and 90 minutes), while activity over the glandular lumen increased with time. The pathway of intracellular transport to the glandular lumen appeared to be via small cytoplasmic vesicles on both days five and six of pregnancy. Additional pathways for transport of the labeled protein to the glandular lumen appeared to be present in the form of the large vesicles on day five and granules on day six of pregnancy.Throughout the peri-implantation period, mouse uterine glands were active secretory structures in which the mode of secretion was similar to other exocrine cells. Thus, the uterine glands of the mouse must be considered a source of uterine fluid proteins at the time of implantation that may contribute to quantitative changes in these proteins.
    Additional Material: 25 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ar.1091990111
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  • 17
    Electronic Resource
    Electronic Resource
    Trophoblast-decidual cell interactions and establishment of maternal blood circulation in the parietal yolk sac placenta of the rat (1987)
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 217 (1987), S. 203-219 
    Details
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Implantation sites from rats were studied on days 6, 7, and 8 of pregnancy to determine the sequence of events in the formation of blood spaces in the trophoblast that is part of the parietal wall of the yolk sac placenta and to determine how trophoblast gains access to maternal blood. The maternal blood flowing through these spaces is the source of nutrients that reach the embryo via the visceral endoderm. Tissues were prepared for light microscopy, scanning electron microscopy, and transmission electron microscopy. Trophoblast blood spaces are derived from the lateral intercellular spaces of trophoblast cells and are present in a collapsed condition until day 8, when maternal vessels are tapped by trophoblast. These spaces than contain circulating maternal blood, and trophoblast cells reflect adaptations for metabolic exchange including thinning of trophoblast covering Reichert's membrane and the appearance of numerous fenestrations, with and without diaphragms, in the areas where trophoblast is attenuated. Between days 6 and 7 decidual cells appear to form a barrier between the maternal circulation and trophoblast. On day 7, however, decidual cell processes penetrate the residual uterine luminal epithelial basal lamina, and then the decidual cells that are juxtaposed to trophoblast undergo degradative changes that resemble apoptosis. There is condensation of cytoplasmic contents, fragmentation of the cells, and phagocytosis of the fragments by trophoblast. Some decidual cells are interposed between endothelial cells in the walls of maternal vessels as early as day 7. Trophoblast may gain access to the maternal vessels by replacing decidual cells or by direct imposition of trophoblast cell processes between endothelial cells.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ar.1092170213
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  • 18
    Electronic Resource
    Electronic Resource
    Differentiation of trophoblast of the baboon blastocyst (1989)
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 225 (1989), S. 329-340 
    Details
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The structure of trophoblast of the baboon blastocyst undergoes a number of maturational changes from the early blastocyst to the late blastocyst stage. The striking expansion of the blastocyst that occurs during the preimplan tation period is accompanied by the development of an extensive endocytic apparatus. Cationized ferritin labels coated depressions and vesicles near the apical cell surface, numerous uncoated tubules and larger apical vesicles, and multivesicular bodies within trophoblast cells. Basally and laterally the labeled components are primarily small uncoated vesicles and tubules. Small, discrete clusters of ferritin particles were seen within the basolateral compartment between trophoblast and its basal lamina and beneath trophoblast cells that do not have a basal lamina. The results indicate that ingested materials may be directed in two pathways, one involving breakdown within the lysosomal system and one involving transcytosis. The zona pellucida is a trilaminar structure consisting of a fibrillar outer layer that often contains spermatozoa, an intermediate zone, and an inner layer containing columns of dense zonal material. Loss of the zona occurs after expansion of the blastocyst and development of the endocytic organelles. During the late blastocyst stage, syncytial trophoblast differentiates at the margin of the polar trophoblast. Because blastocysts were flushed from the uterus, it could not be determined whether azonal blastocysts had been adherent to the uterine surface prior to collection.
    Additional Material: 16 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ar.1092250409
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  • 19
    Electronic Resource
    Electronic Resource
    Differentiation of the inner cell mass of the baboon blastocyst (1990)
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 226 (1990), S. 237-248 
    Details
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: During the blastocyst stage of development in the baboon, the inner cell mass changes from an irregular accumulation of cells within the cavity of the blastocyst to a disk at one side of the blastocyst and finally to a spherial mass of epiblast cells exhibiting a distinct polarity. The cells that will become the primitive endoderm are first seen as flattened but undifferentiated cells on the cavity side of the disk-shaped inner cell mass. After endoderm cells develop their typical cytological characteristics, they extend well beyond the inner cell mass to form parietal endoderm. A basal lamina develops associated with the epiblast cells and mural trophoblast, but not with either parietal or visceral endoderm. Cytological differentiation of inner cell mass cells includes increased numbers of polyribosomes and a change in mitochondria from long, convoluted structures to short, more typical shapes. Evidence that epiblast is polarized is seen by the late zonal blastocyst stage. Apical junctional complexes develop within the center of the epiblast. These junctions presage the development of the potential amniotic cavity. Large vacuoles containing cell debris, some of which contain nuclear fragments, are present at all stages. Extensive cell death occurs during growth of the blastocyst, but the pattern appears to be random and products of cell death are readily phagocytized by adjacent cells.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ar.1092260213
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  • 20
    Electronic Resource
    Electronic Resource
    Comparative studies on the endometrium of delayed implantationSupported by a grant from the National Science Foundation. (1961)
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 139 (1961), S. 483-497 
    Details
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ar.1091390405
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