Wu Yanqi, Cheng Tianhong, Chen Qianyu, Gao Bryan, Stewart Alastair G, Lee Peter V S
Department of Biomedical Engineering, University of Melbourne, Melbourne, VIC 3010, Australia.
Biomicrofluidics. 2020 Feb 18;14(1):014114. doi: 10.1063/1.5138662. eCollection 2020 Jan.
The cytoskeletal mechanics and cell mechanical properties play an important role in cellular behaviors. In this study, in order to provide comprehensive insights into the relationship between different cytoskeletal components and cellular elastic moduli, we built a phase-modulated surface acoustic wave microfluidic device to measure cellular compressibility and a microfluidic micropipette-aspiration device to measure cellular Young's modulus. The microfluidic devices were validated based on experimental data and computational simulations. The contributions of structural cytoskeletal actin filament and microtubule to cellular compressibility and Young's modulus were examined in MCF-7 cells. The compressibility of MCF-7 cells was increased after microtubule disruption, whereas actin disruption had no effect. In contrast, Young's modulus of MCF-7 cells was reduced after actin disruption but unaffected by microtubule disruption. The actin filaments and microtubules were stained to confirm the structural alteration in cytoskeleton. Our findings suggest the dissimilarity in the structural roles of actin filaments and microtubules in terms of cellular compressibility and Young's modulus. Based on the differences in location and structure, actin filaments mainly contribute to tensile Young's modulus and microtubules mainly contribute to compressibility. In addition, different responses to cytoskeletal alterations between acoustophoresis and micropipette aspiration demonstrated that micropipette aspiration was better at detecting the change from actin cortex, while the response to acoustophoresis was governed by microtubule networks.
细胞骨架力学和细胞力学特性在细胞行为中起着重要作用。在本研究中,为了全面深入了解不同细胞骨架成分与细胞弹性模量之间的关系,我们构建了一个相位调制表面声波微流控装置来测量细胞压缩性,并构建了一个微流控微吸管抽吸装置来测量细胞杨氏模量。这些微流控装置基于实验数据和计算模拟进行了验证。在MCF-7细胞中研究了结构性细胞骨架肌动蛋白丝和微管对细胞压缩性和杨氏模量的贡献。微管破坏后MCF-7细胞的压缩性增加,而肌动蛋白破坏则没有影响。相反,肌动蛋白破坏后MCF-7细胞的杨氏模量降低,但不受微管破坏的影响。对肌动蛋白丝和微管进行染色以确认细胞骨架的结构改变。我们的研究结果表明,肌动蛋白丝和微管在细胞压缩性和杨氏模量方面的结构作用存在差异。基于位置和结构的差异,肌动蛋白丝主要影响拉伸杨氏模量,微管主要影响压缩性。此外,声泳和微吸管抽吸对细胞骨架改变的不同反应表明,微吸管抽吸在检测肌动蛋白皮层的变化方面更好,而声泳的反应则由微管网络主导。