Theveneau Eric, Mayor Roberto
Department of Cell and Developmental Biology; University College London; London UK.
Small GTPases. 2010 Sep;1(2):113-117. doi: 10.4161/sgtp.1.2.13673.
For directional cell migration to occur cells must interpret guiding cues present in their environment. Chemotaxis based on negative or positive signals has been long thought as the main driving force of guided cell migration. However during collective cell migration cells do receive information from external signals but also upon interactions with their direct neighbours. These multiple inputs must be translated into intracellular reorganisation in order to promote efficient directional migration. Small GTPases, being involved in establishing cell polarity and regulating protrusive activity, are likely to play a central role in signal integration. Indeed, recent findings from our laboratory indicate that Contact-Inhibition of Locomotion controlled by N-Cadherin and chemotaxis dependent on Sdf1/Cxcr4 signaling converge towards regulation of the localized activity of RhoA and Rac1. All together they establish cell polarity and select well-oriented cell protrusions to ensure directional cell migration.
为了实现定向细胞迁移,细胞必须解读其周围环境中存在的引导线索。长期以来,基于负向或正向信号的趋化作用一直被认为是引导细胞迁移的主要驱动力。然而,在集体细胞迁移过程中,细胞不仅会从外部信号接收信息,还会与直接相邻的细胞发生相互作用。这些多种输入必须转化为细胞内的重组,以促进高效的定向迁移。小GTP酶参与建立细胞极性并调节突出活动,可能在信号整合中发挥核心作用。事实上,我们实验室最近的研究结果表明,由N-钙黏蛋白控制的运动接触抑制和依赖于Sdf1/Cxcr4信号的趋化作用都趋向于对RhoA和Rac1的局部活性进行调节。它们共同建立细胞极性并选择取向良好的细胞突起,以确保细胞的定向迁移。