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RhoA is required for cortical retraction and rigidity during mitotic cell rounding

机译:RhoA是有丝分裂细胞舍入过程中皮质回缩和僵硬所必需的

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Mitotic cell rounding is the process of cell shape change in which a flat interphase cell becomes spherical at the onset of mitosis. Rearrangement of the actin cytoskeleton, de-adhesion, and an increase in cortical rigidity accompany mitotic cell rounding. The molecular mechanisms that contribute to this process have not been defined. We show that RhoA is required for cortical retraction but not de-adhesion during mitotic cell rounding. The mitotic increase in cortical rigidity also requires RhoA, suggesting that increases in cortical rigidity and cortical retraction are linked processes. Rho-kinase is also required for mitotic cortical retraction and rigidity, indicating that the effects of RhoA on cell rounding are mediated through this effector. Consistent with a role for RhoA during mitotic entry, RhoA activity is elevated in rounded, preanaphase mitotic cells. The activity of the RhoA inhibitor p190RhoGAP is decreased due to its serine/threonine phosphorylation at this time. Cumulatively, these results suggest that the mitotic increase in RhoA activity leads to rearrangements of the cortical actin cytoskeleton that promote cortical rigidity, resulting in mitotic cell rounding.
机译:有丝分裂细胞变圆是细胞形状改变的过程,其中扁平的相间细胞在有丝分裂开始时变成球形。肌动蛋白细胞骨架的重排,去粘附和皮质刚度的增加伴随着有丝分裂细胞的舍入。尚未确定导致该过程的分子机制。我们显示,RhoA是皮层收缩所需的,而在有丝分裂细胞的舍入过程中则不需要去粘连。皮质刚度的有丝分裂增加也需要RhoA,表明皮质刚度的增加和皮质回缩是相互联系的过程。 Rho激酶对于有丝分裂皮质的收缩和僵硬也是必需的,这表明RhoA对细胞变圆的作用是通过该效应子介导的。与有丝分裂进入过程中RhoA的作用一致,RhoA活性在圆形,后期的有丝分裂细胞中升高。 RhoA抑制剂p190RhoGAP的活性由于此时的丝氨酸/苏氨酸磷酸化而降低。累积地,这些结果表明RhoA活性的有丝分裂增加导致皮质肌动蛋白细胞骨架的重排,从而促进皮质的刚性,从而导致有丝分裂的细胞变圆。

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