细胞凋亡
免疫系统
发病机制
纤维化
肝纤维化
肝纤维化
巨噬细胞
免疫学
癌症研究
医学
生物
病理
体外
生物化学
作者
Kexin Jia,Zhi Ma,Yinhao Zhang,K. Xie,Jianan Li,Jianzhi Wu,Jiaorong Qu,Fanghong Li,Xiaojiaoyang Li
标识
DOI:10.1016/s1875-5364(24)60674-6
摘要
Liver fibrosis is characterized by chronic inflammatory responses and progressive fibrous scar formation. Macrophages play a central role in the pathogenesis of hepatic fibrosis by reconstructing the immune microenvironment. Picroside II (PIC II), extracted from Picrorhizae Rhizoma, has demonstrated therapeutic potential for various liver damage. However, the mechanisms by which macrophage polarization initiates immune cascades and contributes to the development of liver fibrosis, and whether this process can be influenced by PIC II, remain unclear. In the current study, RNA sequencing and multiple molecular approaches were utilized to explore the underlying mechanisms of PIC II against liver fibrosis in multidrug-resistance protein 2 knockout (Mdr2
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