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癌症相关成纤维细胞通过整合素β3依赖的纤连蛋白组装导致肿瘤侵袭。

Cancer-associated fibroblasts lead tumor invasion through integrin-β3-dependent fibronectin assembly.

作者信息

Attieh Youmna, Clark Andrew G, Grass Carina, Richon Sophie, Pocard Marc, Mariani Pascale, Elkhatib Nadia, Betz Timo, Gurchenkov Basile, Vignjevic Danijela Matic

机构信息

Institut Curie, Paris Sciences et Lettres Research University, Centre National de la Recherche Scientifique, UMR 144, Paris, France

Sorbonne Universités, University Pierre and Marie Curie, University of Paris 6, Institute of Doctoral Studies, Paris, France.

出版信息

J Cell Biol. 2017 Nov 6;216(11):3509-3520. doi: 10.1083/jcb.201702033. Epub 2017 Sep 20.

Abstract

Cancer-associated fibroblasts (CAFs) are the most abundant cells of the tumor stroma. Their capacity to contract the matrix and induce invasion of cancer cells has been well documented. However, it is not clear whether CAFs remodel the matrix by other means, such as degradation, matrix deposition, or stiffening. We now show that CAFs assemble fibronectin (FN) and trigger invasion mainly via integrin-αvβ3. In the absence of FN, contractility of the matrix by CAFs is preserved, but their ability to induce invasion is abrogated. When degradation is impaired, CAFs retain the capacity to induce invasion in an FN-dependent manner. The level of expression of integrins αv and β3 and the amount of assembled FN are directly proportional to the invasion induced by fibroblast populations. Our results highlight FN assembly and integrin-αvβ3 expression as new hallmarks of CAFs that promote tumor invasion.

摘要

癌症相关成纤维细胞(CAFs)是肿瘤基质中最丰富的细胞。它们收缩基质并诱导癌细胞侵袭的能力已有充分记录。然而,尚不清楚CAFs是否通过其他方式重塑基质,如降解、基质沉积或硬化。我们现在表明,CAFs组装纤连蛋白(FN)并主要通过整合素αvβ3触发侵袭。在没有FN的情况下,CAFs对基质的收缩能力得以保留,但其诱导侵袭的能力被消除。当降解受损时,CAFs仍保留以FN依赖方式诱导侵袭的能力。整合素αv和β3的表达水平以及组装的FN量与成纤维细胞群体诱导的侵袭直接相关。我们的结果突出了FN组装和整合素αvβ3表达作为促进肿瘤侵袭的CAFs的新标志。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/307b/5674886/4c868b4a7b02/JCB_201702033_Fig1.jpg

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