Colombié Nathalie, Choesmel-Cadamuro Valérie, Series Jennifer, Emery Gregory, Wang Xiaobo, Ramel Damien
LBCMCP, Centre de Biologie Intégrative (CBI), Université de Toulouse, CNRS, UPS, France.
LBCMCP, Centre de Biologie Intégrative (CBI), Université de Toulouse, CNRS, UPS, France.
Dev Biol. 2017 Mar 1;423(1):12-18. doi: 10.1016/j.ydbio.2017.01.018. Epub 2017 Jan 28.
Collective cell migration is involved in numerous processes both physiological, such as embryonic development, and pathological such as metastasis. Compared to single cell migration, collective motion requires cell behaviour coordination through an as-yet poorly understood but critical cell-cell communication mechanism. Using Drosophila border cell migration, we show here that the small Rho GTPase Cdc42 regulates cell-cell communication. Indeed, we demonstrate that Cdc42 controls protrusion formation in a cell non-autonomous manner. Moreover, we found that the endocytic small GTPase Rab11, controls Cdc42 localisation to the periphery of migrating border cell clusters. Accordingly, over-expression of Cdc42 in border cells rescues the loss of Rab11 function. In addition, we showed that Cdc42 acts upstream of Moesin, a cytoskeletal regulator known to function downstream of rab11. Thus, our study positions Cdc42 as a new key player in cell-cell communication, acting downstream of Rab11.
集体细胞迁移涉及许多生理过程,如胚胎发育,以及病理过程,如转移。与单细胞迁移相比,集体运动需要通过一种尚未完全理解但至关重要的细胞间通讯机制来协调细胞行为。利用果蝇边界细胞迁移,我们在此表明小Rho GTP酶Cdc42调节细胞间通讯。事实上,我们证明Cdc42以非细胞自主方式控制突起形成。此外,我们发现内吞小GTP酶Rab11控制Cdc42定位于迁移的边界细胞簇的周边。因此,在边界细胞中过表达Cdc42可挽救Rab11功能的丧失。此外,我们表明Cdc42在Moesin的上游起作用,Moesin是一种已知在rab11下游起作用的细胞骨架调节因子。因此,我们的研究将Cdc42定位为细胞间通讯中的一个新关键因子,在Rab11下游起作用。