Geng Jiwen, Kang Zhefeng, Sun Qian, Zhang Man, Wang Peng, Li Yupei, Li Jiameng, Su Baihai, Wei Qiang
Department of Nephrology, West China Hospital, Sichuan University, Chengdu, 610041, China.
College of Polymer Science and Engineering, College of Biomedical Engineering, State Key Laboratory of Polymer Materials and Engineering Sichuan University, Chengdu, 610065, China.
Research (Wash D C). 2023;6:0054. doi: 10.34133/research.0054. Epub 2023 Feb 21.
Cellular behaviors and functions can be regulated by mechanical cues from microenvironments, which are transmitted to nucleus through the physical connections of cytoskeletons in the cells. How these physical connections determine transcriptional activity were not clearly known. The actomyosin, which generates intracellular traction force, has been recognized to control the nuclear morphology. Here, we have revealed that microtubule, the stiffest cytoskeleton, is also involved in the process of nuclear morphology alteration. The microtubule negatively regulates the actomyosin-induced nuclear invaginations but not the nuclear wrinkles. Moreover, these nuclear shape changes are proven to mediate the chromatin remodeling, which essentially mediates cell gene expression and phenotype determination. The actomyosin disruption leads to the loss of chromatin accessibility, which can be partly recovered by microtubule interference through nuclear shape control. This finding answers the question of how mechanical cues regulate chromatin accessibility and cell behaviors. It also provides new insights into cell mechanotransduction and nuclear mechanics.
细胞行为和功能可由微环境中的机械信号调节,这些信号通过细胞内细胞骨架的物理连接传递至细胞核。这些物理连接如何决定转录活性尚不清楚。产生细胞内牵引力的肌动球蛋白已被认为可控制细胞核形态。在此,我们发现,最坚硬的细胞骨架微管也参与了细胞核形态改变的过程。微管对肌动球蛋白诱导的核内陷起负调节作用,但对核褶皱不起作用。此外,这些细胞核形状变化被证明可介导染色质重塑,而染色质重塑本质上介导细胞基因表达和表型决定。肌动球蛋白的破坏导致染色质可及性丧失,通过微管干扰细胞核形状可部分恢复这种丧失。这一发现回答了机械信号如何调节染色质可及性和细胞行为的问题。它还为细胞机械转导和核力学提供了新的见解。