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首页> 外文期刊>Integrative Biology: quantitative biosciences from nano to macro >Live-cell subcellular measurement of cell stiffness using a microengineered stretchable micropost array membrane.
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Live-cell subcellular measurement of cell stiffness using a microengineered stretchable micropost array membrane.

机译:使用微工程化的可拉伸微柱阵列膜对细胞刚度进行活细胞亚细胞测量。

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Forces are increasingly recognized as major regulators of cell structure and function, and the mechanical properties of cells, such as cell stiffness, are essential to the mechanisms by which cells sense forces, transmit them to the cell interior or to other cells, and transduce them into chemical signals that impact a spectrum of cellular responses. Here we reported a new whole-cell cell stiffness measurement technique with a subcellular spatial resolution. This technique was based on a novel cell stretching device that allowed for quantitative control and real-time measurements of mechanical stimuli and cellular biomechanical responses. Our strategy involved a microfabricated array of silicone elastomeric microposts integrated onto a stretchable elastomeric membrane. Using a computer-controlled vacuum, this micropost array membrane (mPAM) was activated to apply equibiaxial cell stretching forces to adherent cells attached on the tops of the microposts. The micropost top positions before and after mPAM stretches were recorded using fluorescence microscopy and further utilized to quantify local cell stretching forces and cell area increments. A robust computation scheme was developed and implemented for subcellular quantifications of cell stiffness using the data of local cell stretching forces and cell area increments generated from mPAM cell stretch assays. Our cell stiffness studies using the mPAM revealed strong positive correlations among cell stiffness, cellular traction force, and cell spread area, and illustrated the important functional roles of actin polymerization and myosin II-mediated cytoskeleton contractility in regulating cell stiffness. Collectively, our work reported a new approach for whole-cell stiffness measurements with a subcellular spatial resolution, which would help likely explain the complex biomechanical functions and force-sensing mechanisms of cells and design better materials for cell and tissue engineering and other applications in vivo.Registry Number/Name of Substance 0 (Dimethylpolysiloxanes). 63148-62-9 (baysilon).
机译:越来越多的力量被认为是细胞结构和功能的主要调节者,细胞的机械特性(例如细胞刚度)对于细胞感知力,将力传递至细胞内部或其他细胞并进行转导的机制至关重要。转化成影响一系列细胞反应的化学信号。在这里,我们报告了一种新的具有亚细胞空间分辨率的全细胞细胞硬度测量技术。该技术基于一种新型的细胞拉伸装置,该装置可以定量控制和实时测量机械刺激和细胞生物力学反应。我们的策略涉及将微细的有机硅弹性体微柱阵列集成到可拉伸的弹性体膜上。使用计算机控制的真空,激活该微柱阵列膜(mPAM),以向附着在微柱顶部的贴壁细胞施加等双轴细胞拉伸力。使用荧光显微镜记录在mPAM拉伸之前和之后的micropost顶部位置,并进一步用于量化局部细胞拉伸力和细胞面积增量。使用局部细胞拉伸力和mPAM细胞拉伸测定法产生的细胞面积增量的数据,开发并实施了鲁棒的计算方案,用于细胞硬度的亚细胞定量。我们使用mPAM进行的细胞刚度研究揭示了细胞刚度,细胞牵引力和细胞扩散面积之间的强正相关性,并说明了肌动蛋白聚合和肌球蛋白II介导的细胞骨架收缩在调节细胞刚度中的重要功能。总的来说,我们的工作报告了一种具有亚细胞空间分辨率的全细胞刚度测量的新方法,这可能有助于解释细胞的复杂生物力学功能和力感测机制,并为细胞和组织工程以及其他体内应用设计更好的材料。注册号/物质0的名称(二甲基聚硅氧烷)。 63148-62-9(baysilon)。

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