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定向细胞入侵和不对称黏附驱动 C. elegans 性腺形态发生中的组织伸长和转向。

Directed cell invasion and asymmetric adhesion drive tissue elongation and turning in C. elegans gonad morphogenesis.

机构信息

Department of Cell and Developmental Biology, Faculty of Medicine, Tel Aviv University, Tel Aviv 6997801, Israel.

Faculty of Biology, Technion-Israel Institute of Technology, Haifa 3200003, Israel.

出版信息

Dev Cell. 2022 Sep 12;57(17):2111-2126.e6. doi: 10.1016/j.devcel.2022.08.003. Epub 2022 Aug 31.

Abstract

Development of the C. elegans gonad has long been studied as a model of organogenesis driven by collective cell migration. A somatic cell named the distal tip cell (DTC) is thought to serve as the leader of following germ cells; yet, the mechanism for DTC propulsion and maneuvering remains elusive. Here, we demonstrate that the DTC is not self-propelled but rather is pushed by the proliferating germ cells. Proliferative pressure pushes the DTC forward, against the resistance of the basement membrane in front. The DTC locally secretes metalloproteases that degrade the impeding membrane, resulting in gonad elongation. Turning of the gonad is achieved by polarized DTC-matrix adhesions. The asymmetrical traction results in a bending moment on the DTC. Src and Cdc42 regulate integrin adhesion polarity, whereas an external netrin signal determines DTC orientation. Our findings challenge the current view of DTC migration and offer a distinct framework to understand organogenesis.

摘要

秀丽隐杆线虫的性腺发育一直被作为一个由细胞集体迁移驱动的器官发生模型进行研究。一个名为远端生殖细胞(DTC)的体细胞被认为是后续生殖细胞的领导者;然而,DTC 的推进和操纵机制仍然难以捉摸。在这里,我们证明 DTC 不是自我推进的,而是被增殖的生殖细胞推动的。增殖压力将 DTC 向前推动,对抗前方基底膜的阻力。DTC 局部分泌金属蛋白酶,降解阻碍的膜,导致性腺伸长。性腺的转向是通过极化的 DTC-基质黏附来实现的。不对称的牵引力在 DTC 上产生一个弯矩。Src 和 Cdc42 调节整合素黏附极性,而外部的 netrin 信号决定 DTC 的方向。我们的发现挑战了 DTC 迁移的现有观点,并提供了一个理解器官发生的独特框架。

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