Si-Wu-Tang ameliorates bile duct ligation-induced liver fibrosis via modulating immune environment

免疫系统 肝星状细胞 纤维化 癌症研究 细胞外基质 Fas配体 肝纤维化 CD8型 胆管 细胞凋亡 医学 免疫学 生物 细胞生物学 病理 内科学 程序性细胞死亡 生物化学
作者
Zhi Ma,Xiaoyong Xue,Jinzhao Bai,Yajie Cai,Xuejing Jin,Kexin Jia,Mingning Ding,Xiangjun Lyu,Xiaojiaoyang Li
出处
期刊:Biomedicine & Pharmacotherapy [Elsevier BV]
卷期号:155: 113834-113834 被引量:17
标识
DOI:10.1016/j.biopha.2022.113834
摘要

Si-Wu-Tang (SWT), a traditional Chinese medicine formula firstly recorded from the Tang dynasty, has been reported to alleviate gynecological and liver diseases. We preliminarily demonstrated that SWT could improve liver fibrosis via modulating intestinal microbiota, but little was known about the mechanisms linking its therapeutic effects to the reshaped immune microenvironment within fibrotic livers. Thus, we established a bile duct ligation (BDL)-induced liver fibrosis murine model to evaluate the hepatoprotective effects and potential mechanisms of SWT. The high-performance liquid chromatography, RNA sequencing and other molecular biological techniques were also performed in our study. Our data demonstrated that SWT significantly improved BDL-induced liver fibrosis and inflammatory responses by inhibiting the expression of genes associated with extracellular matrix synthesis and degradation. Combined with the analysis of immune cell infiltration and gene set enrichment analysis (GSEA), we found that SWT remarkably repaired the unbalanced immune microenvironment by modulating the biological functions of different immune cells, especially for macrophages, neutrophils and CD8+ T cells. In addition, SWT significantly inhibited the activation of M2-like macrophages to reduce the release of profibrotic-cytokines and prevented the activation of neutrophils to suppress neutrophil extracellular trap formation. SWT also efficiently promoted the apoptosis of activated hepatic stellate cells via Fas/FasL signaling pathway, which might be mediated by CD8+ tissue-resident memory T cells. In conclusion, our research not only unraveled the intricate mechanisms underlying the hepatoprotective activities of SWT against liver fibrosis but also provided a novel therapeutic strategy for the treatment of liver fibrosis and its relative complications.
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