Crystalline inclusion bodies in rabbit embryos

Development ◽  
1978 ◽  
Vol 44 (1) ◽  
pp. 31-43
Author(s):  
Joseph C. Daniel ◽  
John R. Kennedy

Crystalline inclusion bodies (CIB) may be found as prominent ultrastructural components of the trophoblast cells of rabbit blastocysts and of progestational uterine endometrium. In the work reported here we have sought to describs developmental steps in crystal formation, to correlate these events with embryonic age and to determine if the uterus is essential (either as a source or an environment) for crystal formation in the embryo. CIB, which are of a size and periodicity to make them appear to be clusters or packages of microtubules, are first detectable in embryos 4 days 6 h post coitum and by 4½ days are well established in significant numbers. Another structural component, granular vesicles, may bs seen in embryos as early as 2½ days post coitum, and decrease in number during the same time the CIB are increasing. We believe that the CIB originate from the pre-existing granular vesicles and present electron micrograph evidence of crystal formation progressing from such vesicles. CIB formation does not occur in 4½- to 5-day-old embryos which have been lockedin the oviduct by a suture around the utero-tubal junction. However, when such tube-locked embryos are transplanted into the uterus, they develop crystals within 36 h thereafter.We conclude that the uterus is essential for CIB formation to occur in the rabbit embryo.

Biology ◽  
2021 ◽  
Vol 10 (3) ◽  
pp. 238
Author(s):  
Malgorzata Kloc ◽  
Ahmed Uosef ◽  
Jacek Z. Kubiak ◽  
Rafik M. Ghobrial

Human placenta formation relies on the interaction between fused trophoblast cells of the embryo with uterine endometrium. The fusion between trophoblast cells, first into cytotrophoblast and then into syncytiotrophoblast, is facilitated by the fusogenic protein syncytin. Syncytin derives from an envelope glycoprotein (ENV) of retroviral origin. In exogenous retroviruses, the envelope glycoproteins coded by env genes allow fusion of the viral envelope with the host cell membrane and entry of the virus into a host cell. During mammalian evolution, the env genes have been repeatedly, and independently, captured by various mammalian species to facilitate the formation of the placenta. Such a shift in the function of a gene, or a trait, for a different purpose during evolution is called an exaptation (co-option). We discuss the structure and origin of the placenta, the fusogenic and non-fusogenic functions of syncytin, and the mechanism of cell fusion. We also comment on an alleged danger of the COVID-19 vaccine based on the presupposed similarity between syncytin and the SARS-CoV-2 spike protein.


1976 ◽  
Vol 86 (3) ◽  
pp. 266-269 ◽  
Author(s):  
F. J. Föglein ◽  
Á. Nyitrai ◽  
A. Gulyás ◽  
G. Premecz ◽  
T. Oláh ◽  
...  

1980 ◽  
Vol 26 (4) ◽  
pp. 486-491 ◽  
Author(s):  
Donovan E. Johnson ◽  
Debra M. Niezgodski ◽  
George M. Twaddle

Six oligosporogenic (Spo−) mutant strains of Bacillus thuringiensis were selected from survivors of treatment with N-methyl-N′-nitro-N-nitrosoguanidine. Each strain was blocked at or before stage II of spore development, but all produced typical bipyramidal-shaped crystalline inclusion bodies. Toxicity of the parasporal endotoxin isolated from the mutant strains was assayed by an in vitro technique using cultured insect cells, and was comparable with that of normal wild-type parasporal protein. Multiple parasporal inclusion bodies per cell were often produced, and smaller embedded particles were numerous and distinct.


Development ◽  
2007 ◽  
Vol 134 (9) ◽  
pp. 1809-1817 ◽  
Author(s):  
E. D. Watson ◽  
C. Geary-Joo ◽  
M. Hughes ◽  
J. C. Cross

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