果蝇雄性生殖干细胞生物学的最新进展。

Spermatogenesis Pub Date : 2012-07-01 DOI:10.4161/spmg.21763
Erika L Matunis, Rachel R Stine, Margaret de Cuevas
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引用次数: 0

摘要

干细胞具有非对称分裂能力,能产生自我更新和分化的子细胞,从而维持许多成体组织,但生殖系干细胞(GSC)是干细胞中独一无二的,因为它们能延续物种的基因组。大多数哺乳动物干细胞在其内源性局部微环境(或龛位)中的细胞和分子调控机制是一项相当具有挑战性的研究。不过,对果蝇性腺等干细胞龛位的研究已证明非常有用。在这些组织中,基因干细胞被安置在一个易于识别的龛位中,而对这些细胞及其邻近细胞进行遗传操作的能力,揭示了与一般干细胞相关的几种基本机制。在此,我们总结了果蝇睾丸壁龛中细胞间信号对GSCs的调控,以及与这些信号合作确保生殖细胞存活的细胞内机制的最新研究成果。本综述侧重于成体果蝇睾丸中的GSCs;Zoller和Schulz在本期综述了该组织中的体干细胞。(1) 关于睾丸生态位的整体综述,请参阅de Cuevas和Matunis(2);关于果蝇睾丸的更全面综述,请参阅Fuller(3)以及Davies和Fuller(4)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Recent advances in Drosophila male germline stem cell biology.

Recent advances in Drosophila male germline stem cell biology.

Recent advances in Drosophila male germline stem cell biology.

The ability of stem cells to divide asymmetrically to produce both self-renewing and differentiating daughter cells sustains many adult tissues, but germline stem cells (GSCs) are unique among stem cells as they perpetuate the genome of the species. The cellular and molecular mechanisms regulating most mammalian stem cells in their endogenous local microenvironments, or niches, are quite challenging to study. However, studies of stem cell niches such as those found in the Drosophila gonads have proven very useful. In these tissues, GSCs are housed in a readily identifiable niche, and the ability to genetically manipulate these cells and their neighbors has uncovered several fundamental mechanisms that are relevant to stem cells more generally. Here, we summarize recent work on the regulation of GSCs in the Drosophila testis niche by intercellular signals, and on the intracellular mechanisms that cooperate with these signals to ensure the survival of the germline. This review focuses on GSCs within the adult Drosophila testis; somatic stem cells in this tissue are reviewed by Zoller and Schulz in this issue.(1) For a review of the testis niche as a whole, see de Cuevas and Matunis,(2) and for more comprehensive reviews of the Drosophila testis, refer to Fuller(3) and Davies and Fuller.(4).

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