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旁分泌介导的生殖道发育中的细胞凋亡

Paracrine-mediated apoptosis in reproductive tract development.

作者信息

Roberts L M, Hirokawa Y, Nachtigal M W, Ingraham H A

机构信息

Department of Physiology, University of California, San Francisco, San Francisco, California 94143-0444, USA.

出版信息

Dev Biol. 1999 Apr 1;208(1):110-22. doi: 10.1006/dbio.1998.9190.

Abstract

In mammalian development, the signaling pathways that couple extracellular death signals with the apoptotic machinery are still poorly understood. We chose to examine Müllerian duct regression in the developing reproductive tract as a possible model of apoptosis during morphogenesis. The TGFbeta-like hormone, Müllerian inhibiting substance (MIS), initiates regression of the Müllerian 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 Müllerian duct regression in male embryos beginning at E15. Female Müllerian 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.

摘要

在哺乳动物发育过程中,将细胞外死亡信号与凋亡机制联系起来的信号通路仍未得到充分了解。我们选择研究发育中的生殖道中苗勒管退化,作为形态发生过程中凋亡的一种可能模型。转化生长因子β样激素——苗勒管抑制物质(MIS),启动苗勒管或雌性生殖道原基的退化;这一事件对于正常的雄性性别分化至关重要,在大鼠胚胎期第(E)14至17天之间发生。在此,我们表明,雄性胚胎中从E15开始,苗勒管退化过程中会发生凋亡。暴露于MIS的雌性苗勒管在13小时内也表现出明显的凋亡,这被一种半胱天冬酶抑制剂所阻断。在雄性和雌性中,II型MIS受体仅在围绕管道的间充质细胞层中表达,而凋亡细胞定位于上皮。此外,组织重组实验提供了证据,表明MIS不会直接作用于上皮以诱导凋亡。基于这些数据,我们认为MIS通过改变间充质-上皮相互作用触发细胞死亡。

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