Ultrastructural changes of the early visceral yolk sac layer of mouse embryos after maternal injection of trypan blue

1978 ◽  
Vol 153 (3) ◽  
pp. 287-293 ◽  
Author(s):  
G. Schl�ter
Development ◽  
1964 ◽  
Vol 12 (1) ◽  
pp. 1-14
Author(s):  
Aeleta N. Barber ◽  
Jack C. Geer

Since the discovery of the teratogenicity of trypan blue by Gillman, Gilbert, Gilhnan and Spence (1948) the dye has offered a very concise and convenient method for studying teratogenesis in mammals. Dijkstra & Gillman (1960) fractionated the dye and found that the purple component stimulated the endothelial system in rats, thereby raising the speculation that the varied effects of the dye were caused by contamination. According to our previous experiments (1957, 1963) and those of Wilson, Beaudoin & Free (1959) one aspect of the problem has remained fairly constant, namely, the narrow time limit of the maximal effect of the dye and the stability of the pattern of malformations. Wilson and his associates suggest that the teratogenic effect is due to direct access of the dye to the embryo before the visceral yolk-sac is completely formed.


Development ◽  
1978 ◽  
Vol 43 (1) ◽  
pp. 289-313
Author(s):  
M. Dziadek ◽  
E. Adamson

The localization and synthesis of alphafoetoprotein (AFP) during mouse embryogenesis were studied by immunoperoxidase and by immunoprecipitation after radioactive labelling, using an antiserum prepared against AFP. AFP is first detectable in embryos on the 7th day of gestation (7th day embryos). In 7th and 8th day embryos AFP is confined to visceral (proximal) endoderm cells around the embryonic region of the egg cylinder. Visceral extra-embryonic and parietal (distal) endoderm cells do not contain AFP. By the 9th day of gestation AFP is also present in the extra-embryonic ectoderm, mesoderm and embryonic ectoderm cells around the three cavities of the embryo. These tissues do not synthesize AFP when cultured in isolation, but can adsorb AFP when it is added to the medium. On the 12th day of gestation AFP synthesis is confined to the endoderm layer of the visceral yolk sac. It is concluded that the ability to synthesize AFP is a property which is restricted to the visceral endoderm during early post-implantation development. The presence of AFP in other tissues of the embryo appears to be due to adsorption.


2017 ◽  
Vol 130 (20) ◽  
pp. 3568-3577 ◽  
Author(s):  
Miho Oka ◽  
Keisuke Hashimoto ◽  
Yoshifumi Yamaguchi ◽  
Shin-ichiro Saitoh ◽  
Yuki Sugiura ◽  
...  

Development ◽  
1969 ◽  
Vol 22 (1) ◽  
pp. 115-125
Author(s):  
Marten M. Kernis ◽  
E. Marshall Johnson

Prior to 1927, when Brunschwig proposed that the rat visceral yolk sac is functionally a placenta, it was customary to consider the chorio-allantoic placenta as the primary organ for bringing nourishment to and taking waste from the developing embryo and growing fetus. Eight years later, Everett (1935) predicted that the visceral yolk sac is functionally at least as important as the chorio-allantoic placenta, while Noer & Mossman (1947) suggested that the yolk sac functions differently from the placenta and is therefore complementary in its role. More recently, Halliday (1955) indicated that the proximal yolk sac of the rat is capable of absorbing antibodies by day 17 of gestation. This was confirmed by Brambell & Halliday (1956), who were able to demonstrate that the vitelline epithelium and its underlying vascular system are partly responsible for antibodies penetrating into the embryo.


Development ◽  
1968 ◽  
Vol 19 (2) ◽  
pp. 137-143
Author(s):  
E. Marshall Johnson ◽  
Ralph Spinuzzi

During early gestation in the rat, at the time of rapid embryonic differentiation and prior to the full formation of the chorioallantoic placenta, the function of ‘placental’ nutrition was attributed to the yolk-sac by Brunschwig (1927). Such a paraplacental function of the yolk-sac would assume that nutrients pass through the parietal wall into the yolk-sac cavity and thence into the embryo via the visceral yolk-sac epithelium and its underlying vitelline vessels. Supporting this concept were the findings of Everett (1935) who demonstrated in 13-day embryos that toluidine blue was able to pass into the omphalomesenteric vessels more rapidly than it could reach the umbilical veins via the chorioallantoic placenta. Furthermore, the visceral entodermal cells appeared to exert some selectivity in that trypan blue did not pass into the embryo but was localized in the apical cytoplasm. More recently, Padykula, Deren ' Wilson (1966) demonstrated that the rat yolk-sac concentrated both vitamin B12 and vitamin B12 plus intrinsic factor throughout most of gestation.


Author(s):  
William P. Jollie

A technique has been developed for visualizing antibody against horseradish peroxidase (HRP) in rat visceral yolk sac, the placental membrane across which passive immunity previously has been shown to be transferred from mother to young just prior to birth. Female rats were immunized by injecting both hind foot pads with 1 mg HRP emulsified in complete Freund's adjuvant. They were given a booster of 0.5mg HRP in 0.1 ml normal saline i.v. after one week, then bred and autopsied at selected stages of pregnancy, viz., 12, 1 7 and 22 days post coitum, receiving a second booster, injected as above, five days before autopsy. Yolk sacs were removed surgically and fixed immediately in 2% paraformaldehye, 1% glutaraldehye in 0.1 M phosphate buffer with 0.01% CaCl2 at pH 7.4, room temperature, for 3 hr, rinsed 3X in 0.1 M phosphate buffer plus 5% sucrose, then exposed to 1 mg HRP in 1 ml 0.1 M phosphate buffer at pH 7.4 for 1 hr. They were refixed in aldehydes, as above, for 1 5 min (to assure binding of antigen-antibody complex). Following buffer washes, the tissues were incubated in 3 mg diaminobenzidine tetrahydrochloride and 0.01% H2O2 in 0.05 M Tris-HCl buffer for 30 min. After brief buffer washes, they were postfixed in 2% OsO4. in phosphate buffer at pH 7.4, 4°C for 2 hr, dehydrated through a graded series of ethanols, and embedded in Durcupan. Thin sections were observed and photographed without contrast-enhancement with heavy metals. Cytochemical reaction product marked the site of HRP (i.e., antigen) which, in turn, was present only where it was bound with anti-HRP antibody.


Placenta ◽  
1991 ◽  
Vol 12 (2) ◽  
pp. 143-151 ◽  
Author(s):  
John D. Grubb ◽  
Thomas R. Koszalk ◽  
Joseph J. Drabick ◽  
Robert M. Metrione

Sign in / Sign up

Export Citation Format

Share Document