Jikko Yuya, Deguchi Eriko, Matsuda Kimiya, Hino Naoya, Tsukiji Shinya, Matsuda Michiyuki, Terai Kenta
Department of Pathology and Biology of Diseases, Graduate School of Medicine, Kyoto University, Yoshida-Konoe-Cho, Sakyo-ku, Kyoto 606-8501, Japan.
Center for Living Systems Information Sciences, Graduate School of Biostudies, Kyoto University, Yoshida-Konoe-Cho, Sakyo-ku, Kyoto 606-8501, Japan.
J Cell Sci. 2025 Aug 1;138(15). doi: 10.1242/jcs.263779. Epub 2025 Aug 4.
Collective cell migration is coordinated by the front-to-rear intercellular propagation of EGFR-Ras-ERK pathway activation. However, the molecular mechanisms integrating front-to-rear information into this intercellular signaling cascade, particularly the determinants of cellular front-side specification, remain elusive. We visualized the activity of EGFR, Ras, Rac1 and Rab5A (hereafter Rab5) by using FRET biosensors and chemogenetic tools. Whereas EGFR activation was uniformly observed within cells, Ras activation was biased to the front side within cells. The polarized Ras activation depended on Merlin and Rac1, which also showed front-biased activation. Furthermore, Rab5, a crucial regulator of cell migration, demonstrated similar front-biased activation and was found to function downstream of Ras while being necessary for Rac1 activation. Thus, the positive feedback loop consisting of Ras, Rab5 and Rac1 is activated primarily at the front of collectively migrating cells. These findings offer new spatio-temporal insight into processing front-rear information during collective cell migration.
集体细胞迁移由表皮生长因子受体(EGFR)-Ras-细胞外调节蛋白激酶(ERK)信号通路从前往后的细胞间传播协调。然而,将前后信息整合到这种细胞间信号级联反应中的分子机制,尤其是细胞前端特异性的决定因素,仍然不清楚。我们通过使用荧光共振能量转移(FRET)生物传感器和化学遗传学工具来观察EGFR、Ras、Rac1和Rab5A(以下简称Rab5)的活性。虽然在细胞内观察到EGFR的激活是均匀的,但Ras的激活在细胞内偏向于前端。极化的Ras激活依赖于Merlin和Rac1,它们也表现出前端偏向的激活。此外,Rab5是细胞迁移的关键调节因子,表现出类似的前端偏向激活,并且被发现作用于Ras下游,同时是Rac1激活所必需的。因此,由Ras、Rab5和Rac1组成的正反馈环主要在集体迁移细胞的前端被激活。这些发现为集体细胞迁移过程中前后信息的处理提供了新的时空见解。