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波形蛋白对细胞应激产生的力学贡献。

The Mechanical Contribution of Vimentin to Cellular Stress Generation.

作者信息

van Loosdregt Inge A E W, Weissenberger Giulia, van Maris Marc P F H L, Oomens Cees W J, Loerakker Sandra, Stassen Oscar M J A, Bouten Carlijn V C

机构信息

Department of Biomedical Engineering, Eindhoven University of Technology, P.O. Box 513, Eindhoven 5600 MB, The Netherlands e-mail: .

Department of Biomedical Engineering, Eindhoven University of Technology, P.O. Box 513, Eindhoven MB 5600, The Netherlands e-mail: .

出版信息

J Biomech Eng. 2018 Jun 1;140(6). doi: 10.1115/1.4039308.

Abstract

Contractile stress generation by adherent cells is largely determined by the interplay of forces within their cytoskeleton. It is known that actin stress fibers, connected to focal adhesions, provide contractile stress generation, while microtubules and intermediate filaments provide cells compressive stiffness. Recent studies have shown the importance of the interplay between the stress fibers and the intermediate filament vimentin. Therefore, the effect of the interplay between the stress fibers and vimentin on stress generation was quantified in this study. We hypothesized that net stress generation comprises the stress fiber contraction combined with the vimentin resistance. We expected an increased net stress in vimentin knockout (VimKO) mouse embryonic fibroblasts (MEFs) compared to their wild-type (vimentin wild-type (VimWT)) counterparts, due to the decreased resistance against stress fiber contractility. To test this, the net stress generation by VimKO and VimWT MEFs was determined using the thin film method combined with sample-specific finite element modeling. Additionally, focal adhesion and stress fiber organization were examined via immunofluorescent staining. Net stress generation of VimKO MEFs was three-fold higher compared to VimWT MEFs. No differences in focal adhesion size or stress fiber organization and orientation were found between the two cell types. This suggests that the increased net stress generation in VimKO MEFs was caused by the absence of the resistance that vimentin provides against stress fiber contraction. Taken together, these data suggest that vimentin resists the stress fiber contractility, as hypothesized, thus indicating the importance of vimentin in regulating cellular stress generation by adherent cells.

摘要

贴壁细胞产生的收缩应力在很大程度上取决于其细胞骨架内各种力的相互作用。已知与粘着斑相连的肌动蛋白应力纤维可产生收缩应力,而微管和中间丝则为细胞提供抗压刚度。最近的研究表明应力纤维与中间丝波形蛋白之间相互作用的重要性。因此,本研究对应力纤维与波形蛋白之间的相互作用对应力产生的影响进行了量化。我们假设净应力的产生包括应力纤维收缩与波形蛋白阻力的结合。由于对应力纤维收缩的阻力降低,我们预计波形蛋白基因敲除(VimKO)小鼠胚胎成纤维细胞(MEF)与野生型(波形蛋白野生型(VimWT))相比,净应力会增加。为了验证这一点,我们使用薄膜法结合样本特异性有限元建模来测定VimKO和VimWT MEF产生的净应力。此外,通过免疫荧光染色检查粘着斑和应力纤维的组织情况。VimKO MEF产生的净应力比VimWT MEF高三倍。两种细胞类型之间在粘着斑大小、应力纤维组织和方向上未发现差异。这表明VimKO MEF中净应力产生增加是由于波形蛋白缺失了对应力纤维收缩的阻力。综上所述,这些数据表明波形蛋白如假设的那样抵抗应力纤维的收缩,从而表明波形蛋白在调节贴壁细胞产生细胞应力方面的重要性。

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