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Rho-kinase dependent organization of stress fibers and focal adhesions in cultured fibroblasts.

机译:培养的成纤维细胞中应力纤维和粘着斑的Rho激酶依赖性组织。

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The activation of Rho-kinase is known to modulate the organization of the actin-based cytoskeletal systems, including the formation of stress fibers and focal adhesions. Rho-kinase likely plays a more crucial and complex role in the organization of actin-based cytoskeletal systems than in that of myosin light chain kinase (MLCK). In order to understand the role of Rho-kinase in the organization of stress fibers and focal adhesions, we treated cultured fibroblasts with a Rho-kinase inhibitor and analyzed the stress fiber and focal adhesion organization under conventional fluorescence microscopy and replica electron microscopy. Some of the cells were transfected with GFP-labeled paxillin, actin or alpha-actinin, and the effects of the inhibitor were monitored in the living cells. The Rho-kinase inhibitor caused disassembly of the stress fibers and focal adhesions in the central portion of the cell within 1 h. However, the stress fibers and focal adhesions located in the cell periphery were not as severely affected by the Rho-kinase inhibitor. The time-lapse video recording revealed that when these cells were washed with a fresh medium in order to remove the Rho-kinase inhibitor, the stress fibers and focal adhesions located in the center of the cell gradually reorganized and, within 1.5-2 h, the cells completely recovered. This observation strongly suggests that the activation of Rho-kinase plays an important role in the organization of the central stress fibers and focal adhesions.
机译:已知Rho激酶的激活可调节基于肌动蛋白的细胞骨架系统的组织,包括应力纤维的形成和粘着斑。与肌球蛋白轻链激酶(MLCK)相比,Rho激酶在基于肌动蛋白的细胞骨架系统的组织中可能起着更为关键和复杂的作用。为了了解Rho激酶在应力纤维和粘着斑组织中的作用,我们用Rho激酶抑制剂处理培养的成纤维细胞,并在常规荧光显微镜和复制电子显微镜下分析了应力纤维和粘着斑组织。用GFP标记的paxillin,肌动蛋白或α-肌动蛋白转染一些细胞,并在活细胞中监测抑制剂的作用。 Rho激酶抑制剂在1小时内引起了应力纤维的分解和细胞中心部位的粘连。然而,Rho激酶抑制剂对位于细胞周围的应力纤维和粘着斑的影响并不那么严重。延时录像显示,当用新鲜培养基洗涤这些细胞以去除Rho激酶抑制剂时,位于细胞中心的应力纤维和粘着斑逐渐重组,在1.5至2小时内,细胞完全恢复。该观察结果强烈表明,Rho激酶的活化在中央应力纤维和粘着斑的组织中起重要作用。

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