Gundersen Gregg G, Gomes Edgar R, Wen Ying
Department of Anatomy & Cell Biology, Columbia University, Black Building 1217, 630 W. 168th Street, New York, NY 10032, USA.
Curr Opin Cell Biol. 2004 Feb;16(1):106-12. doi: 10.1016/j.ceb.2003.11.010.
In both dividing and interphase cells, microtubules are remodeled in response to signal transduction pathways triggered by a variety of stimuli. Members of the Rho family of small GTPases have emerged as key intermediates in transmitting signals to cortical factors that mediate capture of dynamic microtubules at specific sites. The specificity of cortical capture appears to be controlled by microtubule tip proteins and cortical receptors that bind these proteins. Recent studies suggest that some of the proteins interacting with microtubule tips behave as bridging proteins between the microtubule tip proteins and their cortical receptors. Such bridging proteins may enhance cortical capture of microtubules directly or indirectly through interactions with the actin cytoskeleton.
在分裂细胞和间期细胞中,微管会根据各种刺激引发的信号转导途径进行重塑。小GTP酶Rho家族的成员已成为将信号传递给皮质因子的关键中间体,这些皮质因子介导动态微管在特定部位的捕获。皮质捕获的特异性似乎由微管末端蛋白和结合这些蛋白的皮质受体控制。最近的研究表明,一些与微管末端相互作用的蛋白充当微管末端蛋白与其皮质受体之间的桥梁蛋白。这种桥梁蛋白可能通过与肌动蛋白细胞骨架的相互作用直接或间接增强微管的皮质捕获。