Non-autonomous role of Cdc42 in cell-cell communication during collective migration

被引:16
作者
Colombie, Nathalie [1 ]
Choesmel-Cadamuro, Valerie [1 ]
Series, Jennifer [1 ]
Emery, Gregory [2 ]
Wang, Xiaobo [1 ]
Ramel, Damien [1 ,3 ,4 ]
机构
[1] Univ Toulouse, CNRS, UPS, LBCMCP,CBI, Toulouse, France
[2] Univ Montreal, Inst Res Immunol & Canc, Montreal, PQ H3C 3J7, Canada
[3] INSERM, U1048, I2MC, F-31300 Toulouse, France
[4] Univ Toulouse III, F-31300 Toulouse, France
基金
加拿大自然科学与工程研究理事会;
关键词
Cdc42; Cell-cell communication; Collective cell migration; Endocytosis; MECHANISMS; MOVEMENT; FORCES;
D O I
10.1016/j.ydbio.2017.01.018
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
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 Rabl I function. In addition, we showed that Cdc42 acts upstream of Moesin, a cytoskeletal regulator known to function downstream of rabl 1. Thus, our study positions Cdc42 as a new key player in cell-cell communication, acting downstream of Rab11.
引用
收藏
页码:12 / 18
页数:7
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