CD147 Promotes CXCL1 Expression and Modulates Liver Fibrogenesis

被引:39
|
作者
Shi, Wen-Pu [1 ]
Ju, Di [2 ]
Li, Hao [1 ]
Yuan, Lin [3 ]
Cui, Jian [1 ]
Luo, Dan [1 ]
Chen, Zhi-Nan [1 ]
Bian, Huijie [1 ]
机构
[1] Fourth Mil Med Univ, Natl Translat Sci Ctr Mol Med, Dept Cell Biol, State Key Lab Canc Biol, Xian 710032, Shaanxi, Peoples R China
[2] Shaanxi Univ Chinese Med, Basic Med Coll, Dept Physiol, Xianyang 712046, Peoples R China
[3] 457 Hosp PLA, Clin Lab, Wuhan 430000, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
CD147; CXCL1; hepatic stellate cells; fibrosis; HEPATIC STELLATE CELLS; IN-VITRO; FIBROSIS; MICE; REVERSIBILITY; CANCER; ANGIOGENESIS; ACTIVATION; CHEMOKINES; INVASION;
D O I
10.3390/ijms19041145
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Activated hepatic stellate cells (HSCs) release pro-inflammatory and pro-fibrogenic factors. CXC chemokine-ligand-1 (CXCL1) is expressed on HSCs. We previously found that the CD147 is overexpressed in activated HSCs. In this study, we showed an important role of CD147 in promoting liver fibrosis by activating HSCs and upregulating expression of chemokines. Specifically, we found that CD147 specific deletion in HSCs mice alleviated CCl4-induced liver fibrosis and inhibited HSCs activation. Overexpression of CD147 upregulated the secretion of CXCL1. Meanwhile, CXCL1 promoted HSCs activation through autocrine. Treating with PI3K/AKT inhibitor could effectively suppress CD147-induced CXCL1 expression. Taken together, these findings suggest that CD147 regulates CXCL1 release in HSCs by PI3K/AKT signaling. Inhibition of CD147 attenuates CCl4-induced liver fibrosis and inflammation. Therefore, administration of targeting CD147 could be a promising therapeutic strategy in liver fibrosis.
引用
收藏
页数:14
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