Wolfenson Haguy, Meacci Giovanni, Liu Shuaimin, Stachowiak Matthew R, Iskratsch Thomas, Ghassemi Saba, Roca-Cusachs Pere, O'Shaughnessy Ben, Hone James, Sheetz Michael P
Department of Biological Sciences, Columbia University, New York, New York 10027, USA.
The Nanomedicine Center for Mechanobiology Directing the Immune Response, Columbia University, New York, New York 10027, USA.
Nat Cell Biol. 2016 Jan;18(1):33-42. doi: 10.1038/ncb3277. Epub 2015 Nov 30.
Cells test the rigidity of the extracellular matrix by applying forces to it through integrin adhesions. Recent measurements show that these forces are applied by local micrometre-scale contractions, but how contraction force is regulated by rigidity is unknown. Here we performed high temporal- and spatial-resolution tracking of contractile forces by plating cells on sub-micrometre elastomeric pillars. We found that actomyosin-based sarcomere-like contractile units (CUs) simultaneously moved opposing pillars in net steps of ∼2.5 nm, independent of rigidity. What correlated with rigidity was the number of steps taken to reach a force level that activated recruitment of α-actinin to the CUs. When we removed actomyosin restriction by depleting tropomyosin 2.1, we observed larger steps and higher forces that resulted in aberrant rigidity sensing and growth of non-transformed cells on soft matrices. Thus, we conclude that tropomyosin 2.1 acts as a suppressor of growth on soft matrices by supporting proper rigidity sensing.
细胞通过整联蛋白黏附向细胞外基质施加力,以此来检测其硬度。最近的测量结果表明,这些力是由局部微米级收缩施加的,但收缩力如何受硬度调节尚不清楚。在这里,我们通过将细胞接种在亚微米弹性柱上,对收缩力进行了高时空分辨率的跟踪。我们发现,基于肌动球蛋白的肌节样收缩单元(CUs)以约2.5纳米的净步长同时移动相对的柱子,这与硬度无关。与硬度相关的是达到激活α-肌动蛋白募集到CUs的力水平所需的步数。当我们通过耗尽原肌球蛋白2.1来消除肌动球蛋白限制时,我们观察到更大的步长和更高的力,这导致了非转化细胞在软基质上的异常硬度感知和生长。因此,我们得出结论,原肌球蛋白2.1通过支持适当的硬度感知,作为软基质上生长的抑制因子。