Strychalski Wanda, Guy Robert D
Department of Mathematics, Applied Mathematics, and Statistics, Case Western Reserve University, Cleveland, Ohio.
Department of Mathematics, University of California Davis, Davis, California.
Biophys J. 2016 Mar 8;110(5):1168-79. doi: 10.1016/j.bpj.2016.01.012.
Blebs are pressure-driven protrusions that play an important role in cell migration, particularly in three-dimensional environments. A bleb is initiated when the cytoskeleton detaches from the cell membrane, resulting in the pressure-driven flow of cytosol toward the area of detachment and local expansion of the cell membrane. Recent experiments involving blebbing cells have led to conflicting hypotheses regarding the timescale of intracellular pressure propagation. The interpretation of one set of experiments supports a poroelastic model of the cytoplasm that leads to slow pressure equilibration when compared to the timescale of bleb expansion. A different study concludes that pressure equilibrates faster than the timescale of bleb expansion. To address this discrepancy, a dynamic computational model of the cell was developed that includes mechanics of and the interactions among the cytoplasm, the actin cortex, the cell membrane, and the cytoskeleton. The model results quantify the relationship among cytoplasmic rheology, pressure, and bleb expansion dynamics, and provide a more detailed picture of intracellular pressure dynamics. This study shows the elastic response of the cytoplasm relieves pressure and limits bleb size, and that both permeability and elasticity of the cytoplasm determine bleb expansion time. Our model with a poroelastic cytoplasm shows that pressure disturbances from bleb initiation propagate faster than the timescale of bleb expansion and that pressure equilibrates slower than the timescale of bleb expansion. The multiple timescales in intracellular pressure dynamics explain the apparent discrepancy in the interpretation of experimental results.
泡状凸起是压力驱动的突出物,在细胞迁移中起着重要作用,尤其是在三维环境中。当细胞骨架与细胞膜分离时,泡状凸起开始形成,导致胞质溶胶向分离区域进行压力驱动流动,并使细胞膜局部扩张。最近涉及形成泡状凸起细胞的实验,引发了关于细胞内压力传播时间尺度的相互矛盾的假设。一组实验的解释支持细胞质的多孔弹性模型,与泡状凸起扩张的时间尺度相比,该模型导致压力平衡缓慢。另一项研究得出结论,压力平衡比泡状凸起扩张的时间尺度更快。为了解决这一差异,开发了一个细胞动态计算模型,该模型包括细胞质、肌动蛋白皮质、细胞膜和细胞骨架的力学及其相互作用。模型结果量化了细胞质流变学、压力和泡状凸起扩张动力学之间的关系,并提供了细胞内压力动态的更详细图景。这项研究表明,细胞质的弹性响应减轻了压力并限制了泡状凸起的大小,并且细胞质的渗透性和弹性都决定了泡状凸起的扩张时间。我们具有多孔弹性细胞质的模型表明,泡状凸起起始产生的压力扰动传播速度比泡状凸起扩张的时间尺度快,而压力平衡比泡状凸起扩张的时间尺度慢。细胞内压力动态中的多个时间尺度解释了实验结果解释中明显的差异。