β1 Integrin induces adhesion and migration of human Th17 cells via Pyk2-dependent activation of P2X4 receptor.

Autor: Hamoudi C; Division of Immune and Infectious Diseases, CHU de Quebec Research Center, Quebec City, Quebec, Canada.; ARThrite Center, Laval University, Québec City, Quebec, Canada., Muheidli A; Division of Immune and Infectious Diseases, CHU de Quebec Research Center, Quebec City, Quebec, Canada.; ARThrite Center, Laval University, Québec City, Quebec, Canada., Aoudjit F; Division of Immune and Infectious Diseases, CHU de Quebec Research Center, Quebec City, Quebec, Canada.; ARThrite Center, Laval University, Québec City, Quebec, Canada.; Department of Microbiology-Infectiology and Immunology, Faculty of Medicine, Laval University, Quebec City, Quebec, Canada.
Jazyk: angličtina
Zdroj: Immunology [Immunology] 2023 Jan; Vol. 168 (1), pp. 83-95. Date of Electronic Publication: 2022 Aug 22.
DOI: 10.1111/imm.13563
Abstrakt: Integrin-mediated T-cell adhesion and migration is a crucial step in immune response and autoimmune diseases. However, the underlying signalling mechanisms are not fully elucidated. In this study, we examined the implication of purinergic signalling, which has been associated with T-cell activation, in the adhesion and migration of human Th17 cells across fibronectin, a major matrix protein associated with inflammatory diseases. We showed that the adhesion of human Th17 cells to fibronectin induces, via β1 integrin, a sustained release of adenosine triphosphate (ATP) from the mitochondria through the pannexin-1 hemichannels. Inhibition of ATP release or its degradation with apyrase impaired the capacity of the cells to attach and migrate across fibronectin. Inhibition studies identified a major role for the purinergic receptor P2X4 in T-cell adhesion and migration but not for P2X7 or P2Y 11 receptors. Blockade of P2X4 but not P2X7 or P2Y 11 receptors reduced cell adhesion and migration by inhibiting activation of β1 integrins, which is essential for ligand binding. Furthermore, we found that β1 integrin-induced ATP release, P2X4 receptor transactivation, cell adhesion and migration were dependent on the focal adhesion kinase Pyk2 but not FAK. Finally, P2X4 receptor inhibition also blocked fibronectin-induced Pyk2 activation suggesting the existence of a positive feedback loop of activation between β1 integrin/Pyk2 and P2X4 purinergic signalling pathways. Our findings uncovered an unrecognized link between β1 integrin and P2X4 receptor signalling pathways for promoting T-cell adhesion and migration across the extracellular matrix.
(© 2022 John Wiley & Sons Ltd.)
Databáze: MEDLINE
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