Department of Biological Sciences, Indian Institute of Science Education and Research Kolkata, Nadia, Mohanpur, 741246, India.
Mechanobiology Institute, National University of Singapore, 5A Engineering Drive 1, Singapore, 117411, Singapore.
Cell Mol Life Sci. 2024 Jan 13;81(1):43. doi: 10.1007/s00018-023-05072-4.
Adherent cells ensure membrane homeostasis during de-adhesion by various mechanisms, including endocytosis. Although mechano-chemical feedbacks involved in this process have been studied, the step-by-step build-up and resolution of the mechanical changes by endocytosis are poorly understood. To investigate this, we studied the de-adhesion of HeLa cells using a combination of interference reflection microscopy, optical trapping and fluorescence experiments. We found that de-adhesion enhanced membrane height fluctuations of the basal membrane in the presence of an intact cortex. A reduction in the tether force was also noted at the apical side. However, membrane fluctuations reveal phases of an initial drop in effective tension followed by saturation. The area fractions of early (Rab5-labelled) and recycling (Rab4-labelled) endosomes, as well as transferrin-labelled pits close to the basal plasma membrane, also transiently increased. On blocking dynamin-dependent scission of endocytic pits, the regulation of fluctuations was not blocked, but knocking down AP2-dependent pit formation stopped the tension recovery. Interestingly, the regulation could not be suppressed by ATP or cholesterol depletion individually but was arrested by depleting both. The data strongly supports Clathrin and AP2-dependent pit-formation to be central to the reduction in fluctuations confirmed by super-resolution microscopy. Furthermore, we propose that cholesterol-dependent pits spontaneously regulate tension under ATP-depleted conditions.
黏附细胞通过各种机制,包括胞吞作用,来确保去黏附过程中的膜稳态。尽管已经研究了涉及这个过程的力学-化学反馈,但胞吞作用中机械变化的逐步建立和解决仍知之甚少。为了研究这个问题,我们使用干涉反射显微镜、光阱和荧光实验相结合的方法研究了 HeLa 细胞的去黏附。我们发现,在皮质完整的情况下,去黏附增强了基底膜的膜高度波动。在顶端也注意到了连接力的降低。然而,膜波动揭示了有效张力初始下降然后饱和的阶段。早期(Rab5 标记)和再循环(Rab4 标记)内体以及靠近基底质膜的转铁蛋白标记陷窝的面积分数也短暂增加。在阻断依赖 dynamin 的胞吞陷窝分裂时,波动的调节并没有被阻断,但是敲低 AP2 依赖性陷窝形成会阻止张力恢复。有趣的是,单独耗尽 ATP 或胆固醇并不能抑制调节,但同时耗尽两者则会阻止调节。该数据强烈支持网格蛋白和 AP2 依赖性陷窝形成是减少波动的核心,这一点通过超分辨率显微镜得到了证实。此外,我们提出胆固醇依赖性陷窝在 ATP 耗尽条件下可以自发调节张力。