Kole Thomas P, Tseng Yiider, Huang Lawrence, Katz Joseph L, Wirtz Denis
Department of Chemical and Biomolecular Engineering, The Johns Hopkins University, Baltimore, Maryland 21218, USA.
Mol Biol Cell. 2004 Jul;15(7):3475-84. doi: 10.1091/mbc.e04-03-0218. Epub 2004 May 14.
Local sol-gel transitions of the cytoskeleton modulate cell shape changes, which are required for essential cellular functions, including motility and adhesion. In vitro studies using purified cytoskeletal proteins have suggested molecular mechanisms of regulation of cytoskeleton mechanics; however, the mechanical behavior of living cells and the signaling pathways by which it is regulated remains largely unknown. To address this issue, we used a nanoscale sensing method, intracellular microrheology, to examine the mechanical response of the cell to activation of the small GTPase Rho. We observe that the cytoplasmic stiffness and viscosity of serum-starved Swiss 3T3 cells transiently and locally enhances upon treatment with lysophosphatidic acid, and this mechanical behavior follows a trend similar to Rho activity. Furthermore, the time-dependent activation of Rho decreases the degree of microheterogeneity of the cytoplasm. Our results reveal fundamental differences between intracellular elasticity and cellular tension and suggest a critical role for Rho kinase in the regulation of intracellular mechanics.
细胞骨架的局部溶胶-凝胶转变调节细胞形状变化,而细胞形状变化是包括运动性和黏附在内的基本细胞功能所必需的。使用纯化的细胞骨架蛋白进行的体外研究已经揭示了调节细胞骨架力学的分子机制;然而,活细胞的力学行为及其调节信号通路在很大程度上仍然未知。为了解决这个问题,我们使用了一种纳米级传感方法——细胞内微流变学,来研究细胞对小GTP酶Rho激活的力学响应。我们观察到,用溶血磷脂酸处理血清饥饿的瑞士3T3细胞后,其细胞质的硬度和黏度会瞬时局部增强,并且这种力学行为与Rho活性呈现相似的趋势。此外,Rho的时间依赖性激活降低了细胞质的微异质性程度。我们的结果揭示了细胞内弹性和细胞张力之间的根本差异,并表明Rho激酶在细胞内力学调节中起关键作用。