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整合素内体信号传导抑制失巢凋亡。

Integrin endosomal signalling suppresses anoikis.

作者信息

Alanko Jonna, Mai Anja, Jacquemet Guillaume, Schauer Kristine, Kaukonen Riina, Saari Markku, Goud Bruno, Ivaska Johanna

机构信息

Turku Centre for Biotechnology, University of Turku, Turku FIN-20520, Finland.

VTT Technical Research Centre of Finland, Turku FIN-20520, Finland.

出版信息

Nat Cell Biol. 2015 Nov;17(11):1412-21. doi: 10.1038/ncb3250. Epub 2015 Oct 5.

Abstract

Integrin-containing focal adhesions transmit extracellular signals across the plasma membrane to modulate cell adhesion, signalling and survival. Although integrins are known to undergo continuous endo/exocytic traffic, the potential impact of endocytic traffic on integrin-induced signals is unknown. Here, we demonstrate that integrin signalling is not restricted to cell-ECM adhesions and identify an endosomal signalling platform that supports integrin signalling away from the plasma membrane. We show that active focal adhesion kinase (FAK), an established marker of integrin-ECM downstream signalling, localizes with active integrins on endosomes. Integrin endocytosis positively regulates adhesion-induced FAK activation, which is early endosome antigen-1 and small GTPase Rab21 dependent. FAK binds directly to purified endosomes and becomes activated on them, suggesting a role for endocytosis in enhancing distinct integrin downstream signalling events. Finally, endosomal integrin signalling contributes to cancer-related processes such as anoikis resistance, anchorage independence and metastasis.

摘要

含整合素的粘着斑可跨质膜传递细胞外信号,从而调节细胞粘附、信号传导和存活。虽然已知整合素会经历持续的内吞/外排运输,但内吞运输对整合素诱导信号的潜在影响尚不清楚。在此,我们证明整合素信号传导不限于细胞与细胞外基质(ECM)的粘附,并确定了一个内体信号平台,该平台支持整合素在远离质膜的位置进行信号传导。我们发现,活性粘着斑激酶(FAK)是整合素-ECM下游信号传导的既定标志物,它与活性整合素在内体上共定位。整合素内吞作用正向调节粘附诱导的FAK激活,这依赖于早期内体抗原-1和小GTP酶Rab21。FAK直接与纯化的内体结合并在其上被激活,这表明内吞作用在增强不同的整合素下游信号传导事件中发挥作用。最后,内体整合素信号传导参与了与癌症相关的过程,如失巢凋亡抗性、锚定非依赖性和转移。

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