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Biomedical subjects

G L Vankin

Publications and source records attributed to G L Vankin.

2 recordsLinked to original sources

Developmental studies of the lethal gene Bld in the mouse. I. Post-implantation development of the lethal homozygote.

In matings of Bld/+ x Bld/+ mice a characteristic type of abnormal embryo is found on days 6 and 7 after impregnation which dies at 8 days and accounts for about 25% of all living embryos. These embryos are regarded as the fethal Bld/Bld homozygotes. Before 6 days the embryos appear slightly retarded. Entodermal cells invade the yolk sac and the trophectoderm does not fuse to the uterine decidua. Late on day 6 the yolk sac is filled with a cap of unorganized cells of entodermal origin, surrounded by both a thick membrane of non-living material, corresponding to Reichert's membrane, and external to this a continuous layer of trophectoderm: there is still almost no contact with uterine tissue. At 7 days 10 h amniotic folds are formed. Mesoderm appears occasionally but is not always present; when it appears it does not grow out from its place of origin. Entodermal cells, particularly in the proximal part of the extra-embryonic region, become polyploid. At the same time, the trophectoderm makes contact with the uterine decidua and gives rise to primary giant cells. Twelve hours later, the embryonic cells begin to degenerate, first in the region of the amniotic fold and the mesoderm. The embryo dies shortly afterwards. It is suggested that the primary target tissues affected by the Bld/Bld constitution are trophectoderm and entoderm. Many but not all of the abnormal features appearing later can by ascribed to insufficient nutrition of the embryo, due to failure of attachment of the trophectoderm and the filling of the yolk sac with entodermal cells.

Animals

C-type virus-lymphocyte interactions in developing mouse thymus.

The appearance of C-type virus particles in thymus cells of Swiss mouse embryos, 11.5 to 15.5 days post-conception age (PCA), was studied with the electron microscope. In thymic rudiments of all specimens examined, virus particles were seen in epithelial cytoplasm, budding from epithelial cell surfaces and in extracellular spaces. Lymphoid cells were first seen in thymic rudiments of 13.5 days PCA, and did not display virus particles at this stage. At 14.5 days PCA, thymic lymphocytes had localized plasmalemmal thickenings of high electron-density which were adjacent to extracellular virus particles. Viruses appeared to be penetrating thymic lymphocytes by viropexis in embryos of 15.5 days PCA. At this stage, many lymphocytes also had cytoplasmic virus-containing vesicles and viral buds at their surfaces. These observations suggest the possibility that, in embryos, C-type viruses are transmitted horizontally from thymic epithelium to early populations of thymic lymphocytes.

Animals