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Nonlinear displacement of ventral stress fibers under externally applied lateral force by an atomic force microscope.

机译:原子力显微镜在外施加侧向力下腹部应力纤维的非线性位移。

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Actin-based stress fibers (SFs) have fundamental importance in the maintenance of mechanical stability of living cells. Several in vitro measurements of their elastic properties have therefore been made, but direct mechanical manipulation of individual SFs in vivo for the determination of their mechanical properties has not been attempted. No less important is a search for the possible formation of a global mechanical network involving SFs and other intracellular filamentous components. In this article, we present an application of atomic force microscopy to probe into a live cell and laterally push selected SFs in a fibroblast cells (VNOf 06 fibroblast-like cells derived from rat vomeronasal tissue) transfected with a green fluorescent protein-beta-actin gene. The transfected cells were transferred to a serum-depleted medium before the atomic force microscope manipulation. The lateral displacement of the SFs under a point loading condition recorded on a fluorescence microscope revealed both linear and nonlinear displacements against the contour distance from the point of force loading. The nonlinear displacements of the SFs were attributed to their association with a cortical actomyosin-cell membrane complex that effectively pulled them back as a 2D thin plate.
机译:基于肌动蛋白的应力纤维(SFS)在维持活细胞机械稳定性方面具有根本重要性。因此,已经进行了其弹性性能的几种体外测量,但尚未尝试在体内进行各个SFS的机械操作,以确定它们的机械性能。不太重要的是寻找可能形成涉及SFS和其他细胞内丝状组分的全局机械网络。在本文中,我们展示了原子力显微镜的施加到探针到活细胞中,并在成纤维细胞中横向推动选择的SFS(VNOF 06成纤维细胞样衍生自用于大鼠茂物组织的细胞),用绿色荧光蛋白-β-肌动蛋白转染基因。在原子力显微镜操作之前将转染的细胞转移至血清贫化培养基。在荧光显微镜上记录的点加载条件下SFS的横向位移揭示了与力负载点的轮廓距离的线性和非线性位移。 SFS的非线性位移归因于其与皮质肌动素 - 细胞膜复合物的关系,其有效地将它们作为2D薄板拉回。

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