Department of Biomedical Engineering, Boston University, Boston, Massachusetts, USA.
Biophys J. 2011 Aug 3;101(3):622-30. doi: 10.1016/j.bpj.2011.06.051.
The vessel wall experiences progressive stiffening with age and the development of cardiovascular disease, which alters the micromechanical environment experienced by resident vascular smooth muscle cells (VSMCs). In vitro studies have shown that VSMCs are sensitive to substrate stiffness, but the exact molecular mechanisms of their response to stiffness remains unknown. Studies have also shown that cell-cell interactions can affect mechanotransduction at the cell-substrate interface. Using flexible substrates, we show that the expression of proteins associated with cell-matrix adhesion and cytoskeletal tension is regulated by substrate stiffness, and that an increase in cell density selectively attenuates some of these effects. We also show that cell-cell interactions exert a strong effect on cell morphology in a substrate-stiffness dependent manner. Collectively, the data suggest that as VSMCs form cell-cell contacts, substrate stiffness becomes a less potent regulator of focal adhesion signaling. This study provides insight into the mechanisms by which VSMCs respond to the mechanical environment of the blood vessel wall, and point to cell-cell interactions as critical mediators of VSMC response to vascular injury.
血管壁会随着年龄的增长和心血管疾病的发展而逐渐变硬,这改变了驻留的血管平滑肌细胞 (VSMC) 所经历的微机械环境。体外研究表明,VSMC 对基质硬度敏感,但它们对硬度的反应的确切分子机制仍不清楚。研究还表明,细胞间相互作用会影响细胞-基质界面的力学转导。我们使用柔性基底表明,与细胞-基质黏附及细胞骨架张力相关的蛋白的表达受基底硬度调节,而细胞密度的增加则选择性地减弱了其中的一些作用。我们还表明,细胞间相互作用以基底硬度依赖的方式对细胞形态产生强烈影响。总的来说,这些数据表明,随着 VSMC 形成细胞-细胞接触,基质硬度对焦点黏附信号的调节作用减弱。本研究深入了解了 VSMC 对血管壁力学环境的反应机制,并指出细胞间相互作用是 VSMC 对血管损伤反应的关键介质。