Pankov Roumen, Endo Yukinori, Even-Ram Sharona, Araki Masaru, Clark Katherine, Cukierman Edna, Matsumoto Kazue, Yamada Kenneth M
Craniofacial Developmental Biology and Regeneration Branch, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD 20892, USA.
J Cell Biol. 2005 Aug 29;170(5):793-802. doi: 10.1083/jcb.200503152.
Directional migration moves cells rapidly between points, whereas random migration allows cells to explore their local environments. We describe a Rac1 mechanism for determining whether cell patterns of migration are intrinsically random or directionally persistent. Rac activity promoted the formation of peripheral lamellae that mediated random migration. Decreasing Rac activity suppressed peripheral lamellae and switched the cell migration patterns of fibroblasts and epithelial cells from random to directionally persistent. In three-dimensional rather than traditional two-dimensional cell culture, cells had a lower level of Rac activity that was associated with rapid, directional migration. In contrast to the directed migration of chemotaxis, this intrinsic directional persistence of migration was not mediated by phosphatidylinositol 3'-kinase lipid signaling. Total Rac1 activity can therefore provide a regulatory switch between patterns of cell migration by a mechanism distinct from chemotaxis.
定向迁移使细胞在不同点之间快速移动,而随机迁移则使细胞能够探索其局部环境。我们描述了一种Rac1机制,用于确定细胞迁移模式是内在随机的还是方向持续的。Rac活性促进了介导随机迁移的外周板层的形成。降低Rac活性可抑制外周板层,并将成纤维细胞和上皮细胞的细胞迁移模式从随机转变为方向持续。在三维而非传统二维细胞培养中,细胞的Rac活性水平较低,这与快速定向迁移相关。与趋化性的定向迁移不同,这种迁移的内在方向持续性不是由磷脂酰肌醇3'-激酶脂质信号介导的。因此,总的Rac1活性可以通过一种不同于趋化性的机制在细胞迁移模式之间提供一种调节开关。