Literature DB >> 6825925

Cell interactions influence the fate of mouse blastomeres undergoing the transition from the 16- to the 32-cell stage.

M H Johnson, C A Ziomek.   

Abstract

Newly formed polar and apolar 1/16 blastomeres were isolated and cultured singly, or in various combinations, through division to form 32-cell blastomeres. The morphology of the resulting cell cluster appeared to depend upon the nature and composition of the cell combination used. In most polar + apolar couplets, the polar cell enveloped the apolar cell, and following division, a 4/32 cluster was thereby generated containing two trophectoderm-like external cells derived from the polar cell and two ICM-like internal cells derived from the apolar cells. A polar cell cultured in isolation divided to give either two trophectoderm-like external cells or a trophectoderm-like cell and an ICM-like cell. Two polar cells cultured together generated clusters in which the ratio of trophectoderm-like:ICM-like cells was 4:0 or 3:1. Most apolar cells cultured together in couplets polarized, and generated 4/32 clusters containing either purely trophectoderm-like or a mixture of trophectoderm- and ICM-like cells. The results are consistent with the notion that continuing interactions between polar and apolar cells are necessary to maintain their respective fates as trophectoderm and ICM, and that in the absence of these interactions polar cells can generate ICM cells by a differentiative division and apolar cells can generate trophectoderm cells by polarizing in response to asymmetric cell contacts.

Entities:  

Mesh:

Year:  1983        PMID: 6825925     DOI: 10.1016/0012-1606(83)90019-2

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  22 in total

1.  Epigenetic Interactions and Gene Expression in Peri-Implantation Mouse Embryo Development.

Authors:  Jean J Latimer; Roger A Pedersen
Journal:  Mod Cell Biol       Date:  1993

2.  Development of Reichert's membrane in the early mouse embryo.

Authors:  M Salamat; N Miosge; R Herken
Journal:  Anat Embryol (Berl)       Date:  1995-09

3.  Fluorescent latex microparticles: A non-invasive short-term cell lineage marker suitable for use in the mouse early embryo.

Authors:  Tom P Fleming; Martin A George
Journal:  Rouxs Arch Dev Biol       Date:  1987-01

4.  The segregation of inner and outer cells in porcine embryos follows a different pattern compared to the segregation in mouse embryos.

Authors:  Marleen Boerjan; Geertruy Te Kronnie
Journal:  Rouxs Arch Dev Biol       Date:  1993-01

5.  Trophectoderm regeneration to support full-term development in the inner cell mass isolated from bovine blastocyst.

Authors:  Nanami Kohri; Hiroki Akizawa; Sakie Iisaka; Hanako Bai; Yojiro Yanagawa; Masashi Takahashi; Masaya Komatsu; Masahito Kawai; Masashi Nagano; Manabu Kawahara
Journal:  J Biol Chem       Date:  2019-11-08       Impact factor: 5.157

Review 6.  Activin/Nodal signalling before implantation: setting the stage for embryo patterning.

Authors:  Costis Papanayotou; Jérôme Collignon
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2014-12-05       Impact factor: 6.237

Review 7.  Developmental control of human preimplantation embryos: a comparative approach.

Authors:  J Tesarík
Journal:  J In Vitro Fert Embryo Transf       Date:  1988-12

Review 8.  Creation of trophectoderm, the first epithelium, in mouse preimplantation development.

Authors:  Yusuke Marikawa; Vernadeth B Alarcon
Journal:  Results Probl Cell Differ       Date:  2012

Review 9.  Intercellular interactions, position, and polarity in establishing blastocyst cell lineages and embryonic axes.

Authors:  Robert O Stephenson; Janet Rossant; Patrick P L Tam
Journal:  Cold Spring Harb Perspect Biol       Date:  2012-11-01       Impact factor: 10.005

Review 10.  Establishment of trophectoderm and inner cell mass lineages in the mouse embryo.

Authors:  Yusuke Marikawa; Vernadeth B Alarcón
Journal:  Mol Reprod Dev       Date:  2009-11       Impact factor: 2.609

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