https://scholars.lib.ntu.edu.tw/handle/123456789/516843
標題: | Cooperative recruitment of Arl4A and Pak1 to the plasma membrane contributes to sustained Pak1 activation for cell migration | 作者: | Chen, Kuan-Jung Chiang, Tsai-Chen Yu, Chia-Jung Fang-Jen Scott Lee |
關鍵字: | ADP-ribosylation factor; Cell migration; GTPase; Pak1; Ras superfamily | 公開日期: | 2020 | 出版社: | COMPANY BIOLOGISTS LTD | 卷: | 133 | 期: | 3 | 來源出版物: | Journal of cell science | 摘要: | Cell migration requires the coordination of multiple signaling pathways involved in membrane dynamics and cytoskeletal rearrangement. The Arf-like small GTPase Arl4A has been shown to modulate actin cytoskeleton remodeling. However, evidence of the function of Arl4A in cell migration is insufficient. Here, we report that Arl4A acts with the serine/threonine protein kinase Pak1 to modulate cell migration through their cooperative recruitment to the plasma membrane. We first observed that Arl4A and its isoform Arl4D interact with Pak1 and Pak2 and showed that Arl4A recruits Pak1 and Pak2 to the plasma membrane. The fibronectin-induced Pak1 localization at the plasma membrane is reduced in Arl4A-depleted cells. Unexpectedly, we found that Pak1, but not Arl4A-binding-defective Pak1, can recruit a cytoplasmic myristoylation-deficient Arl4A-G2A mutant to the plasma membrane. Furthermore, we found that the Arl4A-Pak1 interaction, which is independent of Rac1 binding to Pak1, is required for Arl4A-induced cell migration. Thus, we infer that there is feedback regulation between Arl4A and Pak1, in which they mutually recruit each other to the plasma membrane for Pak1 activation, thereby modulating cell migration through direct interaction. |
URI: | https://scholars.lib.ntu.edu.tw/handle/123456789/516843 | ISSN: | 0021-9533 | DOI: | 10.1242/jcs.233361 |
顯示於: | 分子醫學研究所 |
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