Kovaleva Anastasiia, Solomatina Evgeniya, Tlegenova Madina, Saidova Aleena, Vorobjev Ivan A
Department of Biology, Lomonosov Moscow State University, Moscow 119991, Russia.
Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow 119991, Russia.
Int J Mol Sci. 2025 Aug 9;26(16):7701. doi: 10.3390/ijms26167701.
Focal adhesions (FAs) are multi-protein complexes that mediate cell attachment to the extracellular matrix. Their formation and maturation depend on intracellular tension generated by actin filaments interacting with phosphorylated myosin II. Using live-cell and confocal microscopy, we investigated how FA dynamics are regulated by actin polymerization and myosin II-driven contractility. We found that knockdown of myosin II resulted in complete and irreversible disassembly of FAs. However, partial inhibition of myosin II, through either ROCK or myosin light chain kinase (MLCK) inhibitors, leads to gradual FA shrinkage. In contrast, complete inhibition of myosin II phosphorylation causes disassembly of existing FAs, followed by the formation of new, small FAs at the cell periphery. In both cases, FAs formed after inhibition of myosin II phosphorylation exhibited significantly longer lifespans than FAs in control cells. Similarly, partial inhibition of actin polymerization using nanomolar concentrations of latrunculin B or cytochalasin D also promoted the formation of small FAs. Complete and irreversible FA disassembly occurred only when actin filaments were fully disrupted, leading to cell lamella retraction. These findings suggest that actin polymerization at the cell edge is the minimal and sufficient requirement for the assembly of small FAs. Notably, our data demonstrate for the first time that perturbation of the actin-myosin system results in stabilization and prolonged lifespan of small FAs, whereas larger FAs, formed in the presence of myosin II activity, are more dynamic. Together, these results emphasize the essential role of cortical actin organization and myosin II phosphorylation in the maintenance and turnover of FAs.
粘着斑(FAs)是介导细胞与细胞外基质附着的多蛋白复合物。它们的形成和成熟取决于肌动蛋白丝与磷酸化肌球蛋白II相互作用产生的细胞内张力。利用活细胞和共聚焦显微镜,我们研究了粘着斑动力学如何受肌动蛋白聚合和肌球蛋白II驱动的收缩性调节。我们发现,敲低肌球蛋白II会导致粘着斑完全且不可逆地解体。然而,通过ROCK或肌球蛋白轻链激酶(MLCK)抑制剂对肌球蛋白II进行部分抑制,会导致粘着斑逐渐缩小。相反,完全抑制肌球蛋白II磷酸化会导致现有粘着斑解体,随后在细胞周边形成新的小粘着斑。在这两种情况下,抑制肌球蛋白II磷酸化后形成的粘着斑的寿命都明显长于对照细胞中的粘着斑。同样,使用纳摩尔浓度的Latrunculin B或细胞松弛素D对肌动蛋白聚合进行部分抑制也促进了小粘着斑的形成。只有当肌动蛋白丝完全被破坏导致细胞片层回缩时,才会发生完全且不可逆的粘着斑解体。这些发现表明,细胞边缘的肌动蛋白聚合是小粘着斑组装的最低且充分条件。值得注意的是,我们的数据首次证明,肌动蛋白-肌球蛋白系统的扰动会导致小粘着斑的稳定和寿命延长,而在肌球蛋白II活性存在的情况下形成的较大粘着斑则更具动态性。总之,这些结果强调了皮质肌动蛋白组织和肌球蛋白II磷酸化在粘着斑的维持和周转中的重要作用。