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  • 1
    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
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  • 2
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The morphology and development of junctional complexes between blastomeres of the preimplantation rabbit embryo were investigated using several approaches. Electron microscopic examination of embryos stained en bloc with uranyl acetate, and the study of junction permeability using horseradish peroxidase and lanthanum nitrate provided information on structure, intermembrane spacing and permeability of the junctional complexes. In addition, the freeze fracture technique was used with day 5 and day 6 blastocysts, since the large size of these embryos facilitated use of this method. These experiments showed that although rudimentary junctions were present between blastomeres of the early cleavage stages, effective tight junctions were not present until the blastocyst stage. Electron microscopic examination of thin sections revealed apical foci of membrane approximation or “fusion” between trophoblast cells by day 4. Freeze fracturing revealed a lattice of interconnecting ridges (on the A face) and grooves (on the B face) in the apical region between trophoblast cells of the day 5 blastocyst. This lattice formed a continuous band along the apical margin of each cell, and therefore constituted a zonula occludens. The zonula occludens of the day 5 blastocyst averaged 2-3 ridges per lattice, while day 6 blastocysts had lattices that averaged 5-6 ridges. Also seen in the freeze fracture replicas from the day 5 and day 6 blastocysts were local accumulations of intramembranous particles on the A face. These particles were often observed in aggregates similar to those of previously described gap junctions. It could not be determined whether these small regions of particles were true gap junctions or a possible primitive form of gap junction because the complementary pitted surfaces (B face pits) were not demonstrated.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0002-9106
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: In order to extend the cytological information available on the structure of the interhemal membrane in cricetid rodents, in particular, and myomorph rodents, in general, we have examined the fine structure of the placental labyrinth in five genera of cricetid rodents (Lemmus, Dicrostonyx, Clethrionomys, Microtus and Peromyscus) and one genus of murid rodent (Acomys). Small pieces of labyrinth from near-term placentas were fixed in glutaraldehyde and osmium tetroxide and processed for electron microscopy. The interhemal membranes of all the species examined were hemotrichorial. The outermost layer of trophoblast, bordering the maternal blood spaces, was celular and often contained some patent fenestrae, whereas the middle and inner trophoblastic layers were apparently syncytial. The outermost trophoblastic layer of all the species contained abundant granular endoplasmic reticulum. The intercellular space between the outer and middle layers was variable in width, primarily due to the complex folding of the surface of the middle layer. The surfaces of the middle and inner layers were closely apposed. The middle trophoblastic layer in several species contained filamentous “glomerular bodies” and the innermost layer, particularly of Peromyscus, contained smooth membranous whorls. A basal lamina separated the innermost trophoblastic layer from the fetal capillary endothelium. The endothelial cells in most of the species contained fenestrated regions. These observations are compared to those on other hemochorial placentas, and common features of cricetid (and myomorph) rodent placental fine structure are emphasized.
    Type of Medium: Electronic Resource
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