| Literature DB >> 29042996 |
Hongcan Liu1,2, Xingfei Pan3, Hong Cao4, Xin Shu4, Haixia Sun4, Jianxi Lu5, Jiayin Liang1, Ka Zhang4, Fengqin Zhu4, Gang Li4, Qi Zhang5.
Abstract
Hepatic stellate cell (HSC) activation is important in the pathogenesis of liver fibrosis. However, the molecular mechanism of HSC activation is not completely understood. In the present study, it was demonstrated that interleukin-32γ (IL-32γ) is capable of enhancing intefgrin αvβ6 expression by inducing integrin αvβ6 promoter activity in a dose-dependent manner in HSCs. Furthermore, it was determined that nuclear factor κB (NF-κB) activation is required for IL-32γ-induced integrin αvβ6 expression. Increased integrin αvβ6 expression is then able to activate HSCs. These results indicate that NF-κB activation is required for IL-32γ to induce integrin αvβ6 expression and consequently promote HSC activation. Therefore, IL-32γ activates HSCs and therefore may be associated with hepatic fibrogenesis. These results may enable the development of novel effective strategies to treat hepatic fibrosis.Entities:
Keywords: hepatic fibrosis; hepatic stellate cells; integrin αvβ6; interleukin-32γ
Year: 2017 PMID: 29042996 PMCID: PMC5639283 DOI: 10.3892/etm.2017.4956
Source DB: PubMed Journal: Exp Ther Med ISSN: 1792-0981 Impact factor: 2.447