Combedazou Anne, Gayral Stéphanie, Colombié Nathalie, Fougerat Anne, Laffargue Muriel, Ramel Damien
LBCMCP, Centre de Biologie Intégrative (CBI), Université de Toulouse, CNRS, UPS, France.
INSERM, U1048, I2MC and Université Toulouse III, Toulouse, France.
Small GTPases. 2020 Mar;11(2):103-112. doi: 10.1080/21541248.2017.1366965. Epub 2017 Dec 17.
Collective cell migration is a critical mechanism involved in cell movement during various physiological and pathological processes such as angiogenesis and metastasis formation. During collective movement, cells remain functionally connected and can coordinate individual cell behaviors to ensure efficient migration. A cell-cell communication process ensures this complex coordination. Although the mechanisms regulating cell-cell communication remain unclear, recent findings indicate that it is based on acto-myosin cytoskeleton tension transmission from cell to cell through adherens junctions. As for single cell migration, small GTPases of the Rho and Rab families have been shown to be critical regulators of collective motion. Here, we discuss our current understanding on how these small GTPases are themselves regulated and how they control cell-cell communication during collective migration. Moreover, we also shed light on the key role of cell-cell communication and RhoGTPases in the physiological context of endothelial cell migration during angiogenesis.
集体细胞迁移是一种关键机制,参与血管生成和转移形成等各种生理和病理过程中的细胞运动。在集体运动过程中,细胞保持功能连接,并能协调单个细胞行为以确保高效迁移。细胞间通讯过程确保了这种复杂的协调。尽管调节细胞间通讯的机制尚不清楚,但最近的研究结果表明,它基于肌动蛋白-肌球蛋白细胞骨架张力通过黏附连接在细胞间的传递。至于单细胞迁移,Rho和Rab家族的小GTP酶已被证明是集体运动的关键调节因子。在这里,我们讨论了我们目前对这些小GTP酶如何自身调节以及它们如何在集体迁移过程中控制细胞间通讯的理解。此外,我们还阐明了细胞间通讯和RhoGTP酶在血管生成过程中内皮细胞迁移的生理背景下的关键作用。