Graduate School of Science, Hokkaido University, Sapporo 060-0810, Japan.
Biochem Biophys Res Commun. 2010 Dec 17;403(3-4):363-7. doi: 10.1016/j.bbrc.2010.11.036. Epub 2010 Nov 13.
Filamentous actin and myosin-II are major determinants of cell mechanics and are tightly regulated by a small guanosine triphosphatase, RhoA, and its downstream effectors. We examined the effects of constitutively active mutants of RhoA effectors, which have not been reported before, on cortical stiffness of living cells by using scanning probe microscopy, fluorescence microscopy, and truncated mutants of RhoA effectors labeled with a fluorescent protein. Our data indicated that expression of a constitutively active mutant of Dia1, a formin-family actin polymerizer, enhanced cortical stiffness and increased actin filament quantity in cells. Furthermore, expression of a constitutively active mutant of Rho-associated coiled-coil kinase, a myosin-II activator, softened the cell cortex but increased myosin-II activity. Our findings provide new insights into anomalous mechanics of cells, which is a topic of current interest in a variety of biological research fields.
丝状肌动蛋白和肌球蛋白 II 是细胞力学的主要决定因素,它们受到小 GTP 酶 RhoA 和其下游效应物的严格调控。我们使用扫描探针显微镜、荧光显微镜和用荧光蛋白标记的 RhoA 效应物截断突变体,检测了以前尚未报道过的 RhoA 效应物组成性激活突变体对活细胞皮质硬度的影响。我们的数据表明,一种形成蛋白家族肌动蛋白聚合酶 Dia1 的组成性激活突变体的表达增强了细胞皮质的硬度并增加了细胞中的肌动蛋白丝数量。此外,肌球蛋白 II 激活因子 Rho 相关卷曲螺旋激酶组成性激活突变体的表达使细胞皮质变软,但增加了肌球蛋白 II 的活性。我们的发现为细胞异常力学提供了新的见解,这是当前各种生物学研究领域关注的一个课题。