Integrin αVβ' regulates procollagen I production through a non-canonical transforming growth factor β signaling pathway in human hepatic stellate cells

Hepatic stellate cells (HSCs) are thought to play key roles in the development of liver fibrosis. Extensive evidence has established the concept that aV integrins are involved in the activation of latent transforming growth factor 0 (TGF-0), a master regulator of the fibrotic signaling cascade. Based on mRNA and protein expression profiling data, we found that aV01 integrin is the most abundant member of the aV integrin family in either quiescent or TGF-01-activated primary human HSCs. Unexpectedly, either a selective aV01 inhibitor, Compound 8 (C8), or a pan-aV integrin inhibitor, GSK3008348, decreased TGF-01-activated procollagen I production in primary human HSCs, in which the role of 01 integrin was confirmed by ITGB1 siRNA. In contrast with an Activin receptor-like kinase 5 (Alk5) inhibitor, C8 and GSK3008348 failed to inhibit TGF-01 induced SMAD3 and SMAD2 phosphorylation, but inhibited TGF-0-induced phosphorylation of ERK1/2 and STAT3, suggesting that aV01 integrin is involved in non-canonical TGF-0 signaling pathways. Consistently, ITGB1 siRNA significantly decreased phosphorylation of ERK1/2. Furthermore, a selective inhibitor of MEK1/2 blocked TGF-01 induced phosphorylation of ERK1/2 and decreased TGF-01 induced procollagen I production, while a specific inhibitor of STAT3 had no effect on TGF-01 induced procollagen I production. Taken together, current data indicate that aV01 integrin can regulate TGF-0 signaling independent of its reported role in activating latent TGF-0. Our data further support that aV01 inhibition is a promising therapeutic target for the treatment of liver fibrosis.

Automated summary

The study found that αV01 integrin plays a role in non-canonical TGF-0 signaling pathways and that αV01 inhibition may be an effective strategy for the treatment of liver fibrosis.