Derivation in culture of primordial germ cells from cells of the mouse epiblast: phenotypic induction and growth control by Bmp4 signalling

被引:70
作者
Pesce, M [1 ]
Klinger, FG
De Felici, M
机构
[1] Univ Roma Tor Vergata, Dept Publ Hlth & Cell Biol, Sect Histol & Embryol, Rome, Italy
[2] Ist Dermatol Immacolta, Lab Vasc Pathol, I-00167 Rome, Italy
[3] Ctr Cardiol Monzino, Milan, Italy
关键词
primordial germ cells; epiblast; bone morphogmetic protein-4; germ cell lineage; Smad;
D O I
10.1016/S0925-4773(01)00624-4
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Primordial germ cells (PGCs) are the embryonic precursors of the gametes of the adult. PGCs derive from cells of the most proximal part of the cup-shaped epiblast corresponding to the presumptive region of the extraembryonic mesoderm. At 7.2 days post coitum (dpc) a small group of PGCs located at the base of the allantois can be recognised due to a strong alkaline phosphatase activity. Thus far, scant information was available on the mochanism(s) controlling the lineage of PGCs in the mouse embryo. However, results obtained in mice defective for bone morphogenetic protein-4 (Bmp4) secreted molecule revealed that this growth factor has important functions for the derivation of PGCs from extraembryonic mesoderm cells. In this paper, we have studied the effects in culture of Bmp4 on epiblast cells obtained from egg-cylinder stage mouse embryos (5.5-6.0 dpc) and PGCs from 11.5 dpc embryos. We found that Bmp4 treatment enables recruitment of pluripotent cells to a PGC phenotype by a multi-step process involving an initial pre-commitment of epiblast cells and a following stage of PGC phenotypic determination. We further provide evidences that Bmp4 may promote the growth of gonadal PGCs through a Smad1/4 signalling. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:15 / 24
页数:10
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