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Integrating chemotaxis and contact-inhibition during collective cell migration: Small GTPases at work

机译:在集体细胞迁移过程中整合趋化性和接触抑制:工作中的小GTPase

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摘要

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.
机译:为了使定向细胞迁移发生,细胞必须解释其环境中存在的指导信号。长期以来,人们一直认为基于负信号或正信号的趋化性是引导细胞迁移的主要驱动力。但是,在集体细胞迁移过程中,细胞的确会从外部信号中接收信息,但也会与它们的直接邻居互动。这些多个输入必须被翻译成细胞内重组,以促进有效的定向迁移。参与确定细胞极性和调节突出活动的小GTP酶可能在信号整合中发挥核心作用。实际上,我们实验室的最新发现表明,由N-钙黏着蛋白控制的运动的接触抑制和依赖于Sdf1 / Cxcr4信号的趋化性趋向于调节RhoA和Rac1的局部活性。它们共同建立了细胞极性,并选择了定向良好的细胞突起以确保细胞定向迁移。

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