Ezrin becomes restricted to outer cells following asymmetrical division in the preimplantation mouse embryo

被引:131
作者
Louvet, S [1 ]
Aghion, J [1 ]
Santamaria, A [1 ]
Mangeat, P [1 ]
Maro, B [1 ]
机构
[1] UNIV MONTPELLIER 2,CNRS URA 1856,F-34095 MONTPELLIER,FRANCE
关键词
D O I
10.1006/dbio.1996.0186
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
During preimplantation development in the mouse, two phenotypically distinct cell populations appear at the 16-cell stage: nonpolarized inner cells that give rise to the inner cell mass and polarized outer cells that give rise mainly to the trophectoderm. The divergence of these two cell lineages is due to asymmetrical cell divisions during the transition from the 8- to the 16 cell stage which can occur following blastomere polarization. During compaction, at the 8-cell stage, cytoplasmic organelles accumulate in the apical domain, a surface pole of microvilli forms, and blastomeres flatten onto one another. During the division from the 8- to the 16-cell stage, the only asymmetrical structure maintained is the pole of microvilli, At the 16-cell stage, only blastomeres inheriting a large part of this apical structure can reestablish a polarized organization. The mechanisms involved in the formation and stabilization of the apical pole of microvilli are still unknown. Ezrin is an actin-associated protein that has been proposed to play a role in the formation of microvillous structures. This led us to study the expression of ezrin during early development of the mouse embryo. We observed that ezrin mRNA and protein are present in the mouse oocyte and throughout preimplantation embryo development, although the amount of protein present decreases continuously during early development, particularly after the 8-cell stage, at the time of compaction. Two isoforms of ezrin phosphorylated on tyrosine residues are present during all of preimplantation development while a third non-tyrosine-phosphorylated isoform appears at the 8-cell stage and its relative amount increases from the 8-cell stage to the blastocyst stage. Before compaction, ezrin is distributed around the cell cortex. However ezrin becomes restricted to the microvilli of the apical pole after compaction. At later stages, ezrin is found in the microvilli of the apical surface of outer cells. finally, ezrin remains associated with the microvillous pole during the transition from the 8- to 16-cell stage and is found only in the outer cells after division. Thus, ezrin is the first cytocortical protein described that is totally segregated in outer cells at the 16-cell stage after an asymmetrical division. (C) 1996 Academic Press, Inc.
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页码:568 / 579
页数:12
相关论文
共 42 条
[31]   EZRIN NH2-TERMINAL DOMAIN INHIBITS THE CELL EXTENSION ACTIVITY OF THE COOH-TERMINAL DOMAIN [J].
MARTIN, M ;
ANDREOLI, C ;
SAHUQUET, A ;
MONTCOURRIER, P ;
ALGRAIN, M ;
MANGEAT, P .
JOURNAL OF CELL BIOLOGY, 1995, 128 (06) :1081-1093
[32]   ULTRASTRUCTURAL LOCALIZATION OF LECTIN-BINDING SITES ON ZONAE PELLUCIDAE AND PLASMA-MEMBRANES OF MAMMALIAN EGGS [J].
NICOLSON, GL ;
YANAGIMACHI, R ;
YANAGIMACHI, H .
JOURNAL OF CELL BIOLOGY, 1975, 66 (02) :263-274
[33]   QUANTITATIVE CHANGES IN TOTAL RNA, TOTAL POLY(A), AND RIBOSOMES IN EARLY MOUSE EMBRYOS [J].
PIKO, L ;
CLEGG, KB .
DEVELOPMENTAL BIOLOGY, 1982, 89 (02) :362-378
[34]  
REEVE WJD, 1981, J EMBRYOL EXP MORPH, V62, P339
[35]   LOCALIZATION OF NONERYTHROID SPECTRIN AND ACTIN IN MOUSE OOCYTES AND PREIMPLANTATION EMBRYOS [J].
REIMA, I ;
LEHTONEN, E .
DIFFERENTIATION, 1985, 30 (01) :68-75
[36]   A TARGETED MUTATION IN THE MOUSE E-CADHERIN GENE RESULTS IN DEFECTIVE PREIMPLANTATION DEVELOPMENT [J].
RIETHMACHER, D ;
BRINKMANN, V ;
BIRCHMEIER, C .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (03) :855-859
[37]  
SATO N, 1992, J CELL SCI, V103, P131
[38]   CELL CELL CONTACT MODULATION OF MYOSIN ORGANIZATION IN THE EARLY MOUSE EMBRYO [J].
SOBEL, JS .
DEVELOPMENTAL BIOLOGY, 1983, 100 (01) :207-213
[39]   PERTURBATION OF CELL-ADHESION AND MICROVILLI FORMATION BY ANTISENSE OLIGONUCLEOTIDES TO ERM FAMILY MEMBERS [J].
TAKEUCHI, K ;
SATO, N ;
KASAHARA, H ;
FUNAYAMA, N ;
NAGAFUCHI, A ;
YONEMURA, S ;
TSUKITA, S ;
TSUKITA, S .
JOURNAL OF CELL BIOLOGY, 1994, 125 (06) :1371-1384
[40]   ERM FAMILY MEMBERS AS MOLECULAR LINKERS BETWEEN THE CELL-SURFACE GLYCOPROTEIN CD44 AND ACTIN-BASED CYTOSKELETONS [J].
TSUKITA, S ;
OISHI, K ;
SATO, N ;
SAGARA, J ;
KAWAI, A ;
TSUKITA, S .
JOURNAL OF CELL BIOLOGY, 1994, 126 (02) :391-401