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Self-maintained escort cells form a germline stem cell differentiation niche

机译:自我维持的陪伴细胞形成种系干细胞分化的利基

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摘要

Stem cell self-renewal is controlled by concerted actions of niche signals and intrinsic factors in a variety of systems. In the Drosophila ovary, germline stem cells (GSCs) in the niche continuously self-renew and generate differentiated germ cells that interact physically with escort cells (ECs). It has been proposed that escort stem cells (ESCs), which directly contact GSCs, generate differentiated ECs to maintain the EC population. However, it remains unclear whether the differentiation status of germ cells affects EC behavior and how the interaction between ECs and germ cells is regulated. In this study, we have found that ECs can undergo slow cell turnover regardless of their positions, and the lost cells are replenished by their neighboring ECs via self-duplication rather than via stem cells. ECs extend elaborate cellular processes that exhibit extensive interactions with differentiated germ cells. Interestingly, long cellular processes of ECs are absent when GSC progeny fail to differentiate, suggesting that differentiated germ cells are required for the formation or maintenance of EC cellular processes. Disruption of Rho functions leads to the disruption of long EC cellular processes and the accumulation of ill-differentiated single germ cells by increasing BMP signaling activity outside the GSC niche, and also causes gradual EC loss. Therefore, our findings indicate that ECs interact extensively with differentiated germ cells through their elaborate cellular processes and control proper germ cell differentiation. Here, we propose that ECs form a niche that controls GSC lineage differentiation and is maintained by a non-stem cell mechanism.
机译:干细胞的自我更新受到各种系统中利基信号和内在因素的共同作用的控制。在果蝇卵巢中,小生境中的种系干细胞(GSC)不断自我更新并生成分化的生殖细胞,这些细胞与护送细胞(EC)发生物理相互作用。已经提出,直接接触GSC的伴游干细胞(ESC)产生分化的EC以维持EC群体。但是,尚不清楚生殖细胞的分化状态是否会影响EC的行为以及EC与生殖细胞之间的相互作用如何受到调节。在这项研究中,我们发现EC可以不受其位置的影响而经历缓慢的细胞更新,并且丢失的细胞由邻近的EC通过自我复制而不是通过干细胞来补充。 EC扩展了复杂的细胞过程,该过程表现出与分化生殖细胞的广泛相互作用。有趣的是,当GSC后代无法分化时,就不会存在EC的长细胞过程,这表明分化的生殖细胞是EC细胞过程的形成或维持所必需的。 Rho功能的破坏会导致长时间的EC细胞过程破坏,并通过增加GSC利基以外的BMP信号传导活性,使未分化的单个生殖细胞积聚,并导致EC逐渐丧失。因此,我们的发现表明ECs通过其精心设计的细胞过程与分化的生殖细胞广泛相互作用,并控制适当的生殖细胞分化。在这里,我们建议EC形成控制GSC谱系分化和由非干细胞机制维持的利基市场。

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