CAS Key Laboratory of Mechanical Behavior and Design of Materials, Hefei National Laboratory for Physical Science at the Microscale, CAS Center for Excellence in Complex System Mechanics, Department of Modern Mechanics, University of Science and Technology of China, Hefei, China.
CAS Key Laboratory of Mechanical Behavior and Design of Materials, Hefei National Laboratory for Physical Science at the Microscale, CAS Center for Excellence in Complex System Mechanics, Department of Modern Mechanics, University of Science and Technology of China, Hefei, China.
Biophys J. 2020 Oct 6;119(7):1427-1438. doi: 10.1016/j.bpj.2020.07.039. Epub 2020 Aug 20.
Cell durotaxis is an essential process in tissue development. Although the role of cytoskeleton in cell durotaxis has been widely studied, whether cell volume and membrane tension are implicated in cell durotaxis remains unclear. By quantifying the volume distribution during cell durotaxis, we show that the volume of 3T3 fibroblast cells decreases by almost 40% as cells migrate toward stiffer regions of gradient gels. Inhibiting ion transporters that can reduce the amplitude of cell volume decrease significantly suppresses cell durotaxis. However, from the correlation analysis, we find that durotaxis index does not correlate with the cell volume decrease. It scales with the membrane tension difference in the direction of stiffness gradient. Because of the tight coupling between cell volume and membrane tension, inhibition of Na/K ATPase and Na/H exchanger results in smaller volume decrease and membrane tension difference. Collectively, our findings indicate that the polarization of membrane tension is a central regulator of cell durotaxis, and Na/K ATPase and Na/H exchanger can help to maintain the membrane tension polarity.
细胞趋硬性是组织发育的一个基本过程。虽然细胞骨架在细胞趋硬性中的作用已被广泛研究,但细胞体积和膜张力是否参与细胞趋硬性仍不清楚。通过定量分析细胞在趋硬性过程中的体积分布,我们发现 3T3 成纤维细胞在向梯度凝胶中较硬区域迁移时,体积减少了近 40%。抑制可以减小细胞体积减少幅度的离子转运体,显著抑制细胞趋硬性。然而,从相关分析中,我们发现趋硬性指数与细胞体积减少无关。它与沿刚度梯度方向的膜张力差成正比。由于细胞体积和膜张力之间的紧密耦合,抑制 Na/K ATP 酶和 Na/H 交换器会导致较小的体积减少和膜张力差。总之,我们的研究结果表明,膜张力的极化是细胞趋硬性的核心调节剂,而 Na/K ATP 酶和 Na/H 交换器有助于维持膜张力的极性。