细胞生物学
机械敏感通道
细胞周期
细胞周期蛋白
细胞
细胞质
河马信号通路
生物
细胞骨架
细胞生长
细胞内
化学
信号转导
受体
离子通道
遗传学
作者
Nicolas A. Perez-Gonzalez,Nash D. Rochman,Kai Yao,Jiaxiang Tao,Minh-Tam Tran Le,Shannon M. Flanary,Lucia Sablich,Ben Toler,Eliana Crentsil,Felipe Takaesu,Bram Lambrus,Jessie Huang,Vivian Fu,Pragati Chengappa,Tia M. Jones,Andrew J. Holland,Steven S. An,Denis Wirtz,Ryan J. Petrie,Kun‐Liang Guan,Sean X. Sun
标识
DOI:10.1083/jcb.201902067
摘要
How mammalian cells regulate their physical size is currently poorly understood, in part due to the difficulty in accurately quantifying cell volume in a high-throughput manner. Here, using the fluorescence exclusion method, we demonstrate that the mechanosensitive transcriptional regulators YAP (Yes-associated protein) and TAZ (transcriptional coactivator with PDZ-binding motif) are regulators of single-cell volume. The role of YAP/TAZ in volume regulation must go beyond its influence on total cell cycle duration or cell shape to explain the observed changes in volume. Moreover, for our experimental conditions, volume regulation by YAP/TAZ is independent of mTOR. Instead, we find that YAP/TAZ directly impacts the cell division volume, and YAP is involved in regulating intracellular cytoplasmic pressure. Based on the idea that YAP/TAZ is a mechanosensor, we find that inhibiting myosin assembly and cell tension slows cell cycle progression from G1 to S. These results suggest that YAP/TAZ may be modulating cell volume in combination with cytoskeletal tension during cell cycle progression.
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