Si-Wu-Tang attenuates liver fibrosis via regulating lncRNA H19-dependent pathways involving cytoskeleton remodeling and ECM deposition.
10.1016/S1875-5364(24)60560-1
- Author:
Jiaorong QU
1
;
Xiaoyong XUE
1
;
Zhixing WANG
2
;
Zhi MA
1
;
Kexin JIA
1
;
Fanghong LI
3
;
Yinhao ZHANG
1
;
Ruiyu WU
3
;
Fei ZHOU
1
;
Piwen ZHAO
1
;
Xiaojiaoyang LI
4
Author Information
1. School of Life Sciences, Beijing University of Chinese Medicine, Beijing 100029, China.
2. State Key Laboratory of Medical Molecular Biology, Department of Molecular Biology and Biochemistry, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100005, China.
3. School of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing 100029, China.
4. School of Life Sciences, Beijing University of Chinese Medicine, Beijing 100029, China. Electronic address: xiaojiaoyang.li@bucm.edu.cn.
- Publication Type:Journal Article
- Keywords:
Cytoskeleton;
ECM deposition;
Liver fibrosis;
LncRNA H19;
Si-Wu-Tang;
miRNAs
- MeSH:
Humans;
RNA, Long Noncoding/genetics*;
Liver Cirrhosis/genetics*;
Liver/metabolism*;
Hepatic Stellate Cells/pathology*;
MicroRNAs/metabolism*;
Extracellular Matrix/metabolism*;
Drugs, Chinese Herbal
- From:
Chinese Journal of Natural Medicines (English Ed.)
2024;22(1):31-46
- CountryChina
- Language:English
-
Abstract:
Liver fibrosis is a dynamic wound-healing response characterized by the agglutination of the extracellular matrix (ECM). Si-Wu-Tang (SWT), a traditional Chinese medicine (TCM) formula, is known for treating gynecological diseases and liver fibrosis. Our previous studies demonstrated that long non-coding RNA H19 (H19) was markedly upregulated in fibrotic livers while its deficiency markedly reversed fibrogenesis. However, the mechanisms by which SWT influences H19 remain unclear. Thus, we established a bile duct ligation (BDL)-induced liver fibrosis model to evaluate the hepatoprotective effects of SWT on various cells in the liver. Our results showed that SWT markedly improved ECM deposition and bile duct reactions in the liver. Notably, SWT relieved liver fibrosis by regulating the transcription of genes involved in the cytoskeleton remodeling, primarily in hepatic stellate cells (HSCs), and influencing cytoskeleton-related angiogenesis and hepatocellular injury. This modulation collectively led to reduced ECM deposition. Through extensive bioinformatics analyses, we determined that H19 acted as a miRNA sponge and mainly inhibited miR-200, miR-211, and let7b, thereby regulating the above cellular regulatory pathways. Meanwhile, SWT reversed H19-related miRNAs and signaling pathways, diminishing ECM deposition and liver fibrosis. However, these protective effects of SWT were diminished with the overexpression of H19 in vivo. In conclusion, our study elucidates the underlying mechanisms of SWT from the perspective of H19-related signal networks and proposes a potential SWT-based therapeutic strategy for the treatment of liver fibrosis.
