Integrin endosomal signalling suppresses anoikis.

A1 Originalartikel i en vetenskaplig tidskrift (referentgranskad)


Interna författare/redaktörer


Publikationens författare: Alanko, Mai, Jacquemet, Schauer, Kaukonen, Saari, Goud, Ivaska
Publiceringsår: 2015
Tidskrift: Nature Cell Biology
Tidskriftsakronym: Nat Cell Biol
Volym: 17
Nummer: 11
Artikelns första sida, sidnummer: 1412
Artikelns sista sida, sidnummer: 21
ISSN: 1476-4679


Abstrakt

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.

Senast uppdaterad 2019-21-11 vid 03:36