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, Anhui, 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, Anhui, China.
Biophys J. 2021 Dec 21;120(24):5521-5529. doi: 10.1016/j.bpj.2021.11.019. Epub 2021 Nov 25.
The ability of cells to regulate their shape and volume is critical for many cell functions. How endocytosis and exocytosis, as important ways of membrane trafficking, affect cellular volume regulation is still unclear. Here, we develop a theoretical framework to study the dynamics of cell volume, endocytosis, and exocytosis in response to osmotic shocks and mechanical loadings. This model can not only explain observed dynamics of endocytosis and exocytosis during osmotic shocks but also predict the dynamics of endocytosis and exocytosis during cell compressions. We find that a hypotonic shock stimulates exocytosis, while a hypertonic shock stimulates endocytosis; and exocytosis in turn allows cells to have a dramatic change in cell volume but a small change in membrane tension during hyposmotic swelling, protecting cells from rupture under high tension. In addition, we find that cell compressions with various loading speeds induce three distinct dynamic modes of endocytosis and exocytosis. Finally, we show that increasing endocytosis and exocytosis rates reduce the changes in cell volume and membrane tension under fast cell compression, whereas they enhance the changes in cell volume and membrane tension under slow cell compression. Together, our findings reveal critical roles of endocytosis and exocytosis in regulating cell volume and membrane tension.
细胞调节形状和体积的能力对于许多细胞功能至关重要。内吞作用和外排作用作为重要的膜运输方式,如何影响细胞体积调节仍不清楚。在这里,我们开发了一个理论框架来研究细胞体积、内吞作用和外排作用对渗透压冲击和机械加载的动力学响应。该模型不仅可以解释渗透压冲击过程中观察到的内吞作用和外排作用的动力学,还可以预测细胞压缩过程中的内吞作用和外排作用的动力学。我们发现,低渗冲击刺激外排作用,而高渗冲击刺激内吞作用;外排作用反过来使细胞在低渗肿胀时细胞体积发生剧烈变化而膜张力变化较小,从而在高张力下防止细胞破裂。此外,我们发现,具有不同加载速度的细胞压缩会诱导三种不同的内吞作用和外排作用的动态模式。最后,我们表明,增加内吞作用和外排作用的速率可以减少快速细胞压缩下细胞体积和膜张力的变化,而在缓慢细胞压缩下则会增强细胞体积和膜张力的变化。总之,我们的研究结果揭示了内吞作用和外排作用在调节细胞体积和膜张力方面的关键作用。