Desai Aesha, Geraghty Sandra, Dean Delphine
Department of Bioengineering, Clemson University, Clemson, SC 29634, USA.
Department of Bioengineering, Clemson University, Clemson, SC 29634, USA.
J Biomech. 2019 Jan 3;82:337-345. doi: 10.1016/j.jbiomech.2018.11.004. Epub 2018 Nov 22.
Experimental measurements of cellular mechanical properties have shown large variability in whole-cell mechanical properties between cells from a single population. This heterogeneity has been observed in many cell populations and with several measurement techniques but the sources are not yet fully understood. Cell mechanical properties are directly related to the composition and organization of the cytoskeleton, which is physically coupled to neighboring cells through adherens junctions and to underlying matrix through focal adhesion complexes. This high level of heterogeneity may be attributed to varying cellular interactions throughout the sample. We tested the effect of cell-cell and cell-matrix interactions on the mechanical properties of vascular smooth muscle cells (VSMCs) in culture by using antibodies to block N-cadherin and integrin β1 interactions. VSMCs were cultured on substrates of varying stiffness with and without tension. Under each of these conditions, cellular mechanical properties were characterized by performing atomic force microscopy (AFM) and cellular structure was analyzed through immunofluorescence imaging. As expected, VSMC mechanical properties were greatly affected by the underlying culture substrate and applied tension. Interestingly, the cell-to-cell variation in mechanical properties within each sample decreased significantly in the antibody conditions. Thus, the cells grown with blocking antibodies were more homogeneous in their mechanical properties on both glass and soft substrates. This suggests that diversified adhesion binding between cells and the ECM is responsible for a significant amount of mechanical heterogeneity that is observed in 2D cell culture studies.
细胞力学特性的实验测量表明,来自单一群体的细胞之间全细胞力学特性存在很大差异。在许多细胞群体中以及使用多种测量技术时都观察到了这种异质性,但其来源尚未完全了解。细胞力学特性与细胞骨架的组成和组织直接相关,细胞骨架通过黏附连接与相邻细胞物理相连,并通过黏着斑复合物与下方的基质相连。这种高度的异质性可能归因于整个样本中不同的细胞间相互作用。我们通过使用抗体阻断N-钙黏蛋白和整合素β1的相互作用,测试了细胞间和细胞与基质相互作用对培养的血管平滑肌细胞(VSMC)力学特性的影响。将VSMC培养在有张力和无张力的不同硬度的底物上。在每种条件下,通过原子力显微镜(AFM)表征细胞力学特性,并通过免疫荧光成像分析细胞结构。正如预期的那样,VSMC力学特性受到下方培养底物和施加张力的极大影响。有趣的是,在抗体处理条件下,每个样本中力学特性的细胞间差异显著降低。因此,在玻璃和软底物上,用阻断抗体培养的细胞在力学特性上更加均匀。这表明细胞与细胞外基质之间多样化的黏附结合是二维细胞培养研究中观察到的大量力学异质性的原因。