Durkin Charlotte H, Leite Flavia, Cordeiro João V, Handa Yutaka, Arakawa Yoshiki, Valderrama Ferran, Way Michael
Cellular Signalling and Cytoskeletal Function Laboratory, The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.
Cellular Signalling and Cytoskeletal Function Laboratory, The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.
Dev Cell. 2017 May 8;41(3):315-329.e7. doi: 10.1016/j.devcel.2017.04.010.
RhoA-mediated regulation of myosin-II activity in the actin cortex controls the ability of cells to contract and bleb during a variety of cellular processes, including cell migration and division. Cell contraction and blebbing also frequently occur as part of the cytopathic effect seen during many different viral infections. We now demonstrate that the vaccinia virus protein F11, which localizes to the plasma membrane, is required for ROCK-mediated cell contraction from 2 hr post infection. Curiously, F11-induced cell contraction is dependent on RhoC and not RhoA signaling to ROCK. Moreover, RhoC-driven cell contraction depends on the upstream inhibition of RhoD signaling by F11. This inhibition prevents RhoD from regulating its downstream effector Pak6, alleviating the suppression of RhoC by the kinase. Our observations with vaccinia have now demonstrated that RhoD recruits Pak6 to the plasma membrane to antagonize RhoC signaling during cell contraction and blebbing.
RhoA介导的肌动蛋白皮层中肌球蛋白-II活性的调节控制着细胞在多种细胞过程(包括细胞迁移和分裂)中收缩和形成气泡的能力。细胞收缩和气泡形成也经常作为许多不同病毒感染期间所见细胞病变效应的一部分出现。我们现在证明,定位于质膜的痘苗病毒蛋白F11是感染后2小时ROCK介导的细胞收缩所必需的。奇怪的是,F11诱导的细胞收缩依赖于RhoC而非RhoA向ROCK的信号传导。此外,RhoC驱动的细胞收缩依赖于F11对RhoD信号传导的上游抑制。这种抑制作用可防止RhoD调节其下游效应器Pak6,减轻激酶对RhoC的抑制。我们对痘苗病毒的观察现已证明,在细胞收缩和气泡形成过程中,RhoD将Pak6招募到质膜以拮抗RhoC信号传导。