拉明
细胞生物学
细胞骨架
肌动蛋白
核板
机械转化
生物
核运输
细胞核
核定位序列
内膜
肌动蛋白重塑
细胞外
细胞内
核蛋白
肌动蛋白细胞骨架
核心
细胞
遗传学
转录因子
基因
线粒体
作者
Jeong Ki Kim,Arghavan Louhghalam,Geonhui Lee,Benjamin W. Schafer,Denis Wirtz,Dong Hwee Kim
标识
DOI:10.1038/s41467-017-02217-5
摘要
The distinct spatial architecture of the apical actin cables (or actin cap) facilitates rapid biophysical signaling between extracellular mechanical stimuli and intracellular responses, including nuclear shaping, cytoskeletal remodeling, and the mechanotransduction of external forces into biochemical signals. These functions are abrogated in lamin A/C-deficient mouse embryonic fibroblasts that recapitulate the defective nuclear organization of laminopathies, featuring disruption of the actin cap. However, how nuclear lamin A/C mediates the ability of the actin cap to regulate nuclear morphology remains unclear. Here, we show that lamin A/C expressing cells can form an actin cap to resist nuclear deformation in response to physiological mechanical stresses. This study reveals how the nuclear lamin A/C-mediated formation of the perinuclear apical actin cables protects the nuclear structural integrity from extracellular physical disturbances. Our findings highlight the role of the physical interactions between the cytoskeletal network and the nucleus in cellular mechanical homeostasis.
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