Alanko Jonna, Mai Anja, Jacquemet Guillaume, Schauer Kristine, Kaukonen Riina, Saari Markku, Goud Bruno, Ivaska Johanna
Turku Centre for Biotechnology, University of Turku, Turku FIN-20520, Finland.
VTT Technical Research Centre of Finland, Turku FIN-20520, Finland.
Nat Cell Biol. 2015 Nov;17(11):1412-21. doi: 10.1038/ncb3250. Epub 2015 Oct 5.
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.
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。