Departments of Chemistry and Chemical Biology and Physics, Harvard University, Cambridge, MA, USA.
Howard Hughes Medical Institute, Chevy Chase, MD, USA.
Bioessays. 2020 Jan;42(1):e1900142. doi: 10.1002/bies.201900142. Epub 2019 Dec 11.
Cell membranes experience frequent stretching and poking: from cytoskeletal elements, from osmotic imbalances, from fusion and budding of vesicles, and from forces from the outside. Are the ensuing changes in membrane tension localized near the site of perturbation, or do these changes propagate rapidly through the membrane to distant parts of the cell, perhaps as a mechanical mechanism of long-range signaling? Literature statements on the timescale for membrane tension to equilibrate across a cell vary by a factor of ≈10 . This study reviews and discusses how apparently contradictory findings on tension propagation in cells can be evaluated in the context of 2D hydrodynamics and poroelasticity. Localization of tension in the cell membrane is likely critical in governing how membrane forces gate ion channels, set the subcellular distribution of vesicle fusion, and regulate the dynamics of cytoskeletal growth. Furthermore, in this study, it is proposed that cells can actively regulate the degree to which membrane tension propagates by modulating the density and arrangement of immobile transmembrane proteins. Also see the video abstract here https://youtu.be/T6K7AIAqqBs.
来自细胞骨架成分、渗透压失衡、囊泡融合和出芽,以及来自外部的力。这些膜张力的变化是局限于扰动部位附近,还是迅速传播通过细胞膜到达细胞的遥远部位,也许是长距离信号传递的机械机制?关于膜张力在整个细胞中达到平衡的时间尺度的文献陈述相差约 10 倍。本研究综述并讨论了如何根据二维流体动力学和多孔弹性理论来评估细胞中张力传播的明显矛盾的发现。细胞膜中张力的定位对于控制膜力如何控制离子通道的门控、确定囊泡融合的亚细胞分布以及调节细胞骨架生长的动力学可能是至关重要的。此外,在本研究中,提出细胞可以通过调节不可移动的跨膜蛋白的密度和排列来主动调节膜张力传播的程度。也可以在这里查看视频摘要 https://youtu.be/T6K7AIAqqBs。