Paracrine-mediated apoptosis in reproductive tract development

被引:52
作者
Roberts, LM
Hirokawa, Y
Nachtigal, MW
Ingraham, HA
机构
[1] Univ Calif San Francisco, Dept Physiol, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Grad Program Biomed Sci, San Francisco, CA 94143 USA
关键词
Mullerian inhibiting substance; morphogenesis; programmed cell death; epithelial-mesenchymal interactions;
D O I
10.1006/dbio.1998.9190
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
In mammalian development, the signaling pathways that couple extracellular death signals with the apoptotic machinery are still poorly understood. We chose to examine Mullerian duct regression in the developing reproductive tract as a possible model of apoptosis during morphogenesis. The TGF beta-like hormone, Mullerian inhibiting substance (MIS), initiates regression of the Mullerian duct or female reproductive tract anlagen; this event is essential for proper male sexual differentiation and occurs between embryonic days (E) 14 and 17 in the rat. Here, we show that apoptosis occurs during Mullerian duct regression in male embryos beginning at E15. Female Mullerian ducts exposed to MIS also exhibited prominent apoptosis within 13 h, which was blocked by a caspase inhibitor. In both males and females the MIS type-II receptor is expressed exclusively in the mesenchymal cell layer surrounding the duct, whereas apoptotic cells localize to the epithelium. In addition, tissue recombination experiments provide evidence that MIS does not act directly on the epithelium to induce apoptosis Based on these data, we suggest that MIS triggers cell death by altering mesenchymal-epithelial interactions, (C) 1999 Academic Press.
引用
收藏
页码:110 / 122
页数:13
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