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Journal ArticleDOI

Factors affecting the time of formation of the mouse blastocoele.

Rosita Smith, +1 more
- 01 Oct 1977 - 
- Vol. 41, Iss: 1, pp 79-92
TLDR
In normal mouse embryos developing in vivo, the first appearance of the blastocyst cavity was found to be associated more closely with developmental age, judged by cell number, than with chronological age, i.e. elapsed time since ovulation.
Abstract
In normal mouse embryos developing in vivo, the first appearance of the blastocyst cavity was found to be associated more closely with developmental age, judged by cell number, than with chronological age, i.e. elapsed time since ovulation. When development was slowed by in vitro culture, formation of the blastocoele was delayed. However, cell number itself was not a critical factor, since the number of cells per embryo could be doubled or tripled or halved by experimental manipulation without substantially affecting the timing of blastocoele formation. Experiments in which one cell division was suppressed with cytochalasin-B, leading to tetraploidy, showed that the number of cell divisions since fertilization was also not critical. A possible role is suggested either for nucleocytoplasmic ratio, or for the number of nuclear or chromosomal divisions or DNA replications since fertilization, all of which increase during cleavage.

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Citations
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Journal ArticleDOI

The human blastocyst: cell number, death and allocation during late preimplantation development in vitro

TL;DR: The development of 181 surplus human embryos, including both normally and abnormally fertilized, was observed from day 2 to day 5, 6 or 7 in vitro, and there was widespread cell death in both the TE and ICM as evidenced by fragmenting nuclei, which increased substantially by day 7.
Journal ArticleDOI

Development of Early Porcine Embryos In Vitro and In Vivo

TL;DR: Results indicate that despite the lower nuclear numbers caused by in vitro conditions, the cultured embryos were developmentally competent.
Journal ArticleDOI

Zygotic Genome Activation in Vertebrates.

TL;DR: Progress in understanding vertebrate ZGA dynamics in frogs, fish, mice, and humans is reviewed to explore differences and emphasize common features.
Journal ArticleDOI

The preimplantation pig embryo: cell number and allocation to trophectoderm and inner cell mass of the blastocyst in vivo and in vitro.

TL;DR: Although total cell number did not reach in vivo levels, morphological development and cell number increase was sustained better in the immature mice than in vitro and the proportion of ICM cells in blastocysts formed in vitro was in the normal range.
Journal ArticleDOI

Oligosaccharides containing fucose linked α(1–3) and α(1–4) to N-acetylglucosamine cause decompaction of mouse morulae

TL;DR: It is proposed that LNFP III and II inhibit an endogenous lectin-saccharide interaction between membranes involved in the stabilization of compaction, which is associated with the decrease in the ability of calcium-free medium to cause decompaction.
References
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Journal ArticleDOI

An Air-Drying Method for Chromosome Preparations from Mouse Eggs

TL;DR: The eggs, after being washed out from the genital tract, are put into hypotonic (1%) sodium citrate and left to stand at room temperature for 5–15 minutes and the duration of treatment is not very long.
Journal ArticleDOI

Development of blastomeres of mouse eggs isolated at the 4- and 8-cell stage.

TL;DR: Investigations by Seidel and Tarkowski have shown that although the majority of 1/2 blastomeres can regulate and develop into smaller but otherwise normal blastocysts, som e of them give rise to purely trophoblastic vesicles devoid of the inner cell mass.
Journal ArticleDOI

Immunosurgery of mouse blastocyst.

TL;DR: The results suggest that the mouse blastocyst is not permeable for certain antibodies, and the inner cell masses can easily be separated from the remnants of trophoblastic cells and are then able to grow and differentiate in vitro.
Book ChapterDOI

Nutrient requirements for the culture of preimplantation embryos in vitro

W. K. Whitten
TL;DR: All normal mouse embryos develop from the pronuclear stage to blastocysts when cultured in a simple chemically defined medium and a high proportion of these develop into normal mice if introduced into the uteri of pseudopregnant females.
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