Brito Daniela A, Strauss Joshua, Magidson Valentin, Tikhonenko Irina, Khodjakov Alexey, Koonce Michael P
Division of Molecular Medicine, Wadsworth Center, Albany, NY 12201, USA.
Mol Biol Cell. 2005 Jul;16(7):3334-40. doi: 10.1091/mbc.e05-01-0057. Epub 2005 Apr 27.
Overexpression of dynein fragments in Dictyostelium induces the movement of the entire interphase microtubule array. Centrosomes in these cells circulate through the cytoplasm at rates between 0.4 and 2.5 microm/s and are trailed by a comet-tail like arrangement of the microtubule array. Previous work suggested that these cells use a dynein-mediated pulling mechanism to generate this dramatic movement and that similar forces are at work to maintain the interphase MTOC position in wild-type cells. In the present study, we address the nature of the forces used to produce microtubule movement. We have used a laser microbeam to sever the connection between the motile centrosomes and trailing microtubules, demonstrating that the major force for such motility results from a pushing on the microtubules. We eliminate the possibility that microtubule assembly/disassembly reactions are significant contributors to this motility and suggest that the cell cortex figures prominently in locating force-producing molecules. Our findings indicate that interphase microtubules in Dictyostelium are subject to both dynein- and kinesin-like forces and that these act in concert to maintain centrosome position in the cell and to support the radial character of the microtubule network.
在盘基网柄菌中过表达动力蛋白片段会诱导整个间期微管阵列移动。这些细胞中的中心体以0.4至2.5微米/秒的速度在细胞质中循环,并被微管阵列的彗星尾状排列所跟随。先前的研究表明,这些细胞利用动力蛋白介导的拉动机制产生这种剧烈运动,并且类似的力量在维持野生型细胞中间期微管组织中心(MTOC)的位置中起作用。在本研究中,我们探讨了产生微管运动的力的性质。我们使用激光微束切断运动的中心体与尾随微管之间的连接,证明这种运动的主要力量来自对微管的推动。我们排除了微管组装/拆卸反应是这种运动的重要贡献因素的可能性,并表明细胞皮层在定位产生力的分子方面起着重要作用。我们的研究结果表明,盘基网柄菌中间期微管受到类似动力蛋白和驱动蛋白的力量作用,并且这些力量共同作用以维持细胞中的中心体位置并支持微管网络的放射状特征。