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成纤维细胞球体的形成和激活取决于纤连蛋白-整合素相互作用。

Formation and activation of fibroblast spheroids depend on fibronectin-integrin interaction.

作者信息

Salmenperä Pertteli, Kankuri Esko, Bizik Jozef, Sirén Vappu, Virtanen Ismo, Takahashi Seiichiro, Leiss Michael, Fässler Reinhard, Vaheri Antti

机构信息

Haartman Institute, POB 21, FIN-00014 University of Helsinki, Finland.

出版信息

Exp Cell Res. 2008 Nov 15;314(19):3444-52. doi: 10.1016/j.yexcr.2008.09.004. Epub 2008 Sep 19.

Abstract

Clustering of fibroblasts into spheroids induces a massive proinflammatory, proteolytic and growth-factor response, named nemosis, which promotes tumor cell invasiveness and differentiation of leukemia cells. We have now sought to investigate mechanisms leading to the formation of multicellular spheroids and subsequent activation of fibroblasts (nemosis). Cell lines either lacking fibronectin expression (FN-/-) or expressing FN with a mutated integrin-binding site (FNRGE/RGE) were unable to form compact spheroids. Furthermore, inhibition of FN synthesis by siRNA or functional inhibition of FN or its integrins impaired spheroid formation (alpha5, beta1) and quenched fibroblast activation (alphaV). The integrin ligand GRGDSP hexapeptide interfered with spheroid formation and induced activation of fibroblasts. Surprisingly, a 70 kDa FN fragment, which prevents deposition of FN matrix but does not interfere with FN-integrin interaction, prevented spheroid formation only marginally and did not block the activation. Our results present a new mechanism of fibroblast activation, which is initiated by interaction of FN with its integrin receptors.

摘要

成纤维细胞聚集成球体可引发大规模的促炎、蛋白水解和生长因子反应,即所谓的“nemosis”,它能促进肿瘤细胞的侵袭以及白血病细胞的分化。我们现在试图研究导致多细胞球体形成以及随后成纤维细胞激活(nemosis)的机制。缺乏纤连蛋白表达的细胞系(FN-/-)或表达带有突变整合素结合位点的纤连蛋白(FNRGE/RGE)的细胞系均无法形成紧密的球体。此外,通过小干扰RNA抑制纤连蛋白合成或对纤连蛋白及其整合素进行功能抑制,会损害球体形成(α5、β1)并抑制成纤维细胞激活(αV)。整合素配体GRGDSP六肽会干扰球体形成并诱导成纤维细胞激活。令人惊讶的是,一个70 kDa的纤连蛋白片段,它能阻止纤连蛋白基质的沉积,但不干扰纤连蛋白与整合素的相互作用,仅略微阻止球体形成,且不阻断激活。我们的结果提出了一种成纤维细胞激活的新机制,该机制由纤连蛋白与其整合素受体的相互作用引发。

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