IL-32γ promotes integrin αvβ6 expression through the activation of NF-κB in HSCs

被引:9
|
作者
Liu, Hongcan [1 ,2 ]
Pan, Xingfei [3 ]
Cao, Hong [4 ]
Shu, Xin [4 ]
Sun, Haixia [4 ]
Lu, Jianxi [5 ]
Liang, Jiayin [1 ]
Zhang, Ka [4 ]
Zhu, Fengqin [4 ]
Li, Gang [4 ]
Zhang, Qi [5 ]
机构
[1] Sun Yat Sen Univ, Affiliated Hosp 3, Dept Clin Lab, Guangzhou 510630, Guangdong, Peoples R China
[2] Guangzhou Univ Chinese Med, Affiliated Hosp 2, Dept Clin Lab, Guangzhou 510120, Guangdong, Peoples R China
[3] Guangzhou Med Univ, Affiliated Hosp 3, Dept Infect Dis, Guangzhou 510150, Guangdong, Peoples R China
[4] Sun Yat Sen Univ, Affiliated Hosp 3, Dept Infect Dis, 600 Tianhe Rd, Guangzhou 510630, Guangdong, Peoples R China
[5] Sun Yat Sen Univ, Affiliated Hosp 3, Vaccine Res Inst, 600 Tianhe Rd, Guangzhou 510630, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
interleukin-32; gamma; hepatic stellate cells; integrin alpha v beta 6; hepatic fibrosis; HEPATIC STELLATE CELLS; LIVER FIBROSIS; INTERLEUKIN-32; EXPRESSION; CANCER; MECHANISMS; CYTOKINE; ENGAGEMENT; PATHWAY; ALPHA; LX-2;
D O I
10.3892/etm.2017.4956
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
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-32 gamma (IL-32 gamma) is capable of enhancing intefgrin alpha v beta 6 expression by inducing integrin alpha v beta 6 promoter activity in a dose-dependent manner in HSCs. Furthermore, it was determined that nuclear factor kappa B (NF-kappa B)activation is required for IL-32 gamma-induced integrin alpha v beta 6 expression. Increased integrin alpha v beta 6 expression is then able to activate HSCs. These results indicate that NF-kappa B activation is required for IL-32 gamma to induce integrin alpha v beta 6 expression and consequently promote HSC activation. Therefore, IL-32 gamma activates HSCs and therefore may be associated with hepatic fibrogenesis. These results may enable the development of novel effective strategies to treat hepatic fibrosis.
引用
收藏
页码:3880 / 3886
页数:7
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