𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Cell and molecular regulation of the mouse blastocyst

✍ Scribed by Yojiro Yamanaka; Amy Ralston; Robert O. Stephenson; Janet Rossant


Publisher
John Wiley and Sons
Year
2006
Tongue
English
Weight
891 KB
Volume
235
Category
Article
ISSN
1058-8388

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

Animals use diverse strategies to specify tissue lineages during development. A common strategy is to partition maternally supplied and localized lineage determinants into progenitor cells. The mouse embryo appears to use a different, more regulative strategy to specify the first three lineages: the epiblast (EPI: future embryo), the trophectoderm (TE: future placenta), and the primitive endoderm (PE: future yolk sac). These lineages are specified during two successive differentiation steps leading to formation of the blastocyst. Here, we review classic and contemporary models of early lineage specification in the mouse, and describe recent efforts to understand the molecular regulation of these events. We describe evidence that trophectoderm differentiation bears resemblance to the process of epithelialization and describe the importance of apical/basal protein complexes in regulating this process. Next, we present a revised model of PE specification, and describe evidence that PE cells in the inner cell mass sort out to occupy their ultimate position on the surface of the EPI. Finally, we describe factors that reinforce these lineages and three distinct stem cell types that can be isolated from them. Together, these mechanisms guide the differentiation of the first lineages of the mouse and thereby set up tissues that will be important for the first steps of embryonic body patterning. Developmental Dynamics 235:2301–2314, 2006. Β© 2006 Wiley‐Liss, Inc.


πŸ“œ SIMILAR VOLUMES


Mechanisms of cell number regulation in
✍ Evsikov, S.V.; Vagyna, I.N.; Solomko, A.P. πŸ“‚ Article πŸ“… 1996 πŸ› John Wiley and Sons 🌐 English βš– 681 KB

Low viability of manipulated or in vitro cultured embryos is caused primarily by the reduced cell number in the implanting blastocysts. In order to investigate the effect of implantation delay on embryo viability and cell number, mouse blastocysts were transferred into oviducts of day 0 pseudopregna

Trophectoderm cell subpopulations in the
✍ ChΓ‘vez, Daniel J. ;Enders, Allen C. ;Schlafke, Sandra πŸ“‚ Article πŸ“… 1984 πŸ› John Wiley and Sons 🌐 English βš– 472 KB

## Abstract Trophectoderm of the preimplantation mouse blastocyst is composed of two cell subpopulations relative to their proximity to the inner cell mass. The polar trophectoderm overlying the inner cell mass proliferates to form the ectoplacental cone, and the mural trophectoderm endoreplicates

Effect of antimetabolites on programming
✍ McCue, Peter A. ;Sherman, Michael I. πŸ“‚ Article πŸ“… 1982 πŸ› John Wiley and Sons 🌐 English βš– 475 KB πŸ‘ 1 views

## Abstract When early blastocysts are subjected to immunosurgery, the resulting inner cell masses (ICMs) regenerate trophoblast cells. In contrast, ICMs from later blastocysts produce endoderm cells. We have found that if embryos are treated with cycloheximide during the transition from the early

Integrin trafficking regulates adhesion
✍ Schultz, Jeffery F. ;Mayernik, Linda ;Rout, Ujjwal K. ;Armant, D. Randall πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 English βš– 215 KB πŸ‘ 1 views

Trophoblast cells of the peri-implantation blastocyst differentiate from a polarized epithelium, the trophectoderm, into invasive cells having an apical surface occupied by integrins that mediate adhesion to the extracellular matrix. Blastocyst differentiation was assessed during serum-free culture