Zhao Yuanchang, Wang Yongliang, Sarkar Anwesha, Wang Xuefeng
Department of Physics and Astronomy, Iowa State University, 12 Physics Hall, Ames, IA 50011, USA.
Department of Physics and Astronomy, Iowa State University, 12 Physics Hall, Ames, IA 50011, USA; Molecular, Cellular, and Developmental Biology Interdepartmental Program, Molecular Biology Building, Ames, IA 50011, USA.
iScience. 2018 Nov 30;9:502-512. doi: 10.1016/j.isci.2018.11.016. Epub 2018 Nov 12.
Rapid cell migration requires efficient rear de-adhesion. It remains undetermined whether cells mechanically detach or biochemically disassemble integrin-mediated rear adhesion sites in highly motile cells such as keratocytes. Using molecular tension sensor, we calibrated and mapped integrin tension in migrating keratocytes. Our experiments revealed that high-level integrin tension abbreviated as HIT, in the range of 50-100 pN (piconewton) and capable of rupturing integrin-ligand bonds, is exclusively and narrowly generated at cell rear margin during cell migration. Co-imaging of HIT and focal adhesions (FAs) shows that HIT is produced to mechanically peel off FAs that lag behind, and HIT intensity is correlated with the local cell retraction rate. High-level molecular tension was also consistently generated at the cell margin during artificially induced cell front retraction and during keratocyte migration mediated by biotin-streptavidin bonds. Collectively, these experiments provide direct evidence showing that migrating keratocytes concentrate force at the cell rear margin to mediate rear de-adhesion.
快速的细胞迁移需要高效的尾部去黏附。目前仍不确定在诸如角膜细胞等高度迁移性细胞中,细胞是通过机械方式脱离还是通过生化方式拆解整合素介导的尾部黏附位点。我们使用分子张力传感器,对迁移中的角膜细胞中的整合素张力进行了校准和测绘。我们的实验表明,高水平整合素张力(简称为HIT),范围在50-100皮牛顿(piconewton),能够使整合素-配体键断裂,在细胞迁移过程中仅在细胞后缘狭窄区域产生。HIT与黏着斑(FAs)的共成像显示,产生HIT是为了机械性地剥离滞后的黏着斑,且HIT强度与局部细胞回缩率相关。在人工诱导的细胞前缘回缩过程以及生物素-链霉亲和素键介导的角膜细胞迁移过程中,细胞边缘也持续产生高水平分子张力。总的来说,这些实验提供了直接证据,表明迁移中的角膜细胞在细胞后缘集中力量以介导尾部去黏附。