Naringenin is a Potential Immunomodulator for Inhibiting Liver Fibrosis by Inhibiting the cGAS-STING Pathway

被引:29
作者
Chen, Li [1 ]
Xia, Siwei [1 ]
Wang, Shuqi [1 ]
Zhou, Yuanyuan [1 ]
Wang, Feixia [1 ]
Li, Zhanghao [1 ]
Li, Yang [1 ]
Kong, Desong [2 ]
Zhang, Zili [1 ]
Shao, Jiangjuan [1 ]
Xu, Xuefen [1 ]
Zhang, Feng [1 ]
Zheng, Shizhong [1 ]
机构
[1] Nanjing Univ Chinese Med, Sch Pharm, Jiangsu Key Lab Pharmacol & Safety Evaluat Chines, Nanjing, Jiangsu, Peoples R China
[2] Nanjing Univ Chinese Med, Chinese Med Modernizat & Big Data Res Ctr, Nanjing, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Liver fibrosis; cGAS; Naringenin; Inflammation; Hepatic stellate cells; TGF-BETA/SMAD; MODULATION; CELLS;
D O I
10.14218/JCTH.2022.00120
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
Background and Aims: Naringenin is an anti-inflammatory flavonoid that has been studied in chronic liver disease. The mechanism specific to its antifibrosis activity needs further investigation This study was to focused on the cyclic guanosine monophosphate-adenosine monophosphate synthase (cGAS) pathway in hepatic stellate cells and clarified the antifibrosis mechanism of naringenin. Methods: The relationship between the cGAS-stimulator of interferon genes (STING) pathway and liver fibrosis was analyzed using the Gene Expression Omnibus database. Histopathology, immunohistochemistry, fluorescence staining, Western blotting and polymerase chain reaction were performed to assess gene and protein expression levels associated with the cGAS pathway in clinical liver tissue samples and mouse livers. Molecular docking was performed to evaluate the relationship between naringenin and cGAS, and western blotting was performed to study the expression of inflammatory factors downstream of cGAS in vitro. Results: Clinical database analyses showed that the cGAS-STING pathway is involved in the occurrence of chronic liver disease. Naringenin ameliorated liver injury and liver fibrosis, decreased collagen deposition and cGAS expression, and inhibited inflammation in carbon tetrachloride (CCl4)-treated mice. Molecular docking found that cGAS may be a direct target of naringenin. Consistent with the in vivo results, we verified the inhibitory effect of naringenin on activated hepatic stellate cells (HSCs). By using the cGAS-specific agonist double-stranded (ds)DNA, we showed that naringenin attenuated the activation of cGAS and its inflammatory factors affected by dsDNA. We verified that naringenin inhibited the cGAS-STING pathway, thereby reducing the secretion of inflammatory factors by HSCs to ameliorate liver fibrosis. Conclusions: Interrupting the cGAS-STING pathway helped reverse the fibrosis process. Naringenin has potential as an antihepatic fibrosis drug.
引用
收藏
页码:26 / 37
页数:12
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