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Substrate rigidity regulates fibronectin matrix assembly in fibroblasts.

机译:基质的刚性调节成纤维细胞中的纤连蛋白基质组装。

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摘要

Cells sense and respond to the mechanical properties of their microenvironment. We investigated whether these properties affect the ability of cells to assemble a fibrillar fibronectin (FN) matrix. Analysis of matrix assembled by cells grown on FN-coated polyacrylamide gels of varying stiffnesses showed that rigid substrates stimulate FN matrix assembly, whereas assembly is inhibited on softer substrates. Stimulating integrins with Mn 2+ treatment increased FN assembly on softer gels, suggesting that integrin binding is deficient on soft substrates. Guanidine hydrochloride-induced extension of the substrate-bound FN rescued assembly on soft substrates to a similar degree as Mn2+ treatment and also increased the initiation of assembly at FN matrix assembly sites. In contrast, increasing actin-mediated cell contractility did not rescue FN matrix assembly on soft substrates. Thus, rigidity-dependent FN matrix assembly is determined by extracellular events, namely, the engagement of FN by cells and the induction of FN conformational changes. Extensibility of FN in response to substrate stiffness may serve as a mechanosensing mechanism whereby cells use pericellular FN to probe the stiffness of their environment.
机译:细胞感知并响应其微环境的机械特性。我们调查了这些属性是否影响细胞组装纤维状纤连蛋白(FN)基质的能力。由在不同刚度的FN涂层聚丙烯酰胺凝胶上生长的细胞组装的基质的分析表明,刚性基质刺激FN基质的组装,而组装在较软的基质上受到抑制。 Mn 2+处理刺激整联蛋白会增加软凝胶上的FN组装,这表明整联蛋白在软底物上的结合不足。盐酸胍诱导的与基质结合的FN的延伸使软基质上的组装得以恢复,其程度与Mn2 +处理相似,并且还增加了FN基质组装部位的组装起始。相反,增加的肌动蛋白介导的细胞收缩力不能拯救FN基质在软基质上的组装。因此,刚性依赖的FN基质组装是由细胞外事件决定的,即细胞对FN的结合和FN构象变化的诱导。 FN对基质硬度的响应性可作为一种机械传感机制,从而使细胞利用细胞周围的FN探测其环境的硬度。

著录项

  • 作者

    Carraher, Cara L.;

  • 作者单位

    Princeton University.;

  • 授予单位 Princeton University.;
  • 学科 Biology Molecular.
  • 学位 Ph.D.
  • 年度 2013
  • 页码 116 p.
  • 总页数 116
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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