Assembly of tight junctions during early vertebrate development

被引:80
作者
Fleming, TP
Papenbrock, T
Fesenko, I
Hausen, P
Sheth, B
机构
[1] Univ Southampton, Sch Biol Sci, Div Cell Biol, Southampton SO16 7PX, Hants, England
[2] Max Planck Inst Dev Biol, D-72076 Tubingen, Germany
基金
英国惠康基金; 英国医学研究理事会;
关键词
tight junction; embryo; mouse; Xenopus; epithelium;
D O I
10.1006/scdb.2000.0179
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Tight junction formation during development is critical for embryonic patterning and organization. We consider mechanisms of junction biogenesis in cleaving mouse and Xenopus eggs. Junction assembly follows the establishment of cell polarity at 8-cell (mouse) or 2-cell (Xenopus) stages, characterized by sequential membrane delivery of constituents, coordinated by embryonic (mouse) or maternal (Xenopus) expression programmes. Cadherin adhesion is permissive for tight junction construction only in the mouse. Occludin post-translational modification and membrane delivery, mediated by delayed ZO-1 alpha(+) isoform expression in the mouse, provides a mechanism for completion of tight junction biogenesis and sealing; regulating the timing of blastocoel cavitation.
引用
收藏
页码:291 / 299
页数:9
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