Verboon Jeffrey M, Parkhurst Susan M
a Division of Basic Sciences; Fred Hutchinson Cancer Research Center ; Seattle , WA USA.
Small GTPases. 2015;6(1):1-7. doi: 10.4161/21541248.2014.992262.
Repair of wounds to single cells involves dynamic membrane and cytoskeletal rearrangements necessary to seal the wound and repair the underlying cytoskeleton cortex. One group of proteins essential to the cortical remodeling is the Rho family of small GTPases. Recently we showed that the founding members of this GTPases family, Rho, Rac, and Cdc42, are all essential for normal single cell wound repair and accumulate at the wound periphery in distinct temporal/spatial patterns in the Drosophila cell wound model. In addition, these proteins communicate with one another and with the cytoskeleton to regulate their distribution in response to wounds. Unexpectedly, we found evidence for context specific Rho GTPase binding to downstream targets or "effectors" which cannot be explained solely by means of local GTPase activation. Here we discuss these observations in relation to similar studies in single cell wound repair in the Xenopus oocyte, and highlight how these cell wound models serve as powerful tools to understand both cell wound repair and Rho GTPase biology.
单细胞伤口修复涉及动态的膜和细胞骨架重排,这对于封闭伤口和修复潜在的细胞骨架皮层是必要的。对皮层重塑至关重要的一类蛋白质是小GTP酶的Rho家族。最近我们发现,这个GTP酶家族的创始成员Rho、Rac和Cdc42,对于正常的单细胞伤口修复都是必不可少的,并且在果蝇细胞伤口模型中以不同的时空模式聚集在伤口边缘。此外,这些蛋白质相互之间以及与细胞骨架进行通讯,以响应伤口来调节它们的分布。出乎意料的是,我们发现了特定背景下Rho GTP酶与下游靶点或“效应器”结合的证据,这不能仅通过局部GTP酶激活来解释。在这里,我们结合在非洲爪蟾卵母细胞单细胞伤口修复中的类似研究来讨论这些观察结果,并强调这些细胞伤口模型如何作为强大的工具来理解细胞伤口修复和Rho GTP酶生物学。