表观遗传学
免疫系统
透视图(图形)
巨噬细胞
功能(生物学)
生物
后生
疾病
神经科学
免疫学
细胞生物学
医学
遗传学
内科学
基因表达
DNA甲基化
计算机科学
基因
人工智能
体外
作者
Ruizhi Tan,Qianrong Bai,Long-hao Jia,Yibing Wang,Tong Li,Jing‐Yi Lin,Jian Liu,Hong-Wei Su,Fahsai Kantawong,Li Wang
标识
DOI:10.1016/j.biopha.2025.117842
摘要
The interaction between renal intrinsic cells and macrophages plays a crucial role in the onset and progression of kidney diseases. In recent years, epigenetic mechanisms such as DNA methylation, histone modification, and non-coding RNA regulation have become essential windows for understanding these processes. This review focuses on how renal intrinsic cells (including tubular epithelial cells, podocytes, and endothelial cells), renal cancer cells, and mesenchymal stem cells influence the function and polarization status of macrophages through their own epigenetic alterations, and how the epigenetic regulation of macrophages themselves responds to kidney damage, thus participating in renal inflammation, fibrosis, and repair. Moreover, therapeutic studies targeting these epigenetic interaction mechanisms have found that the application of histone deacetylase inhibitors, histone methyltransferase inhibitors, various nanomaterials, and locked nucleic acids against non-coding RNA have positive effects on the treatment of multiple kidney diseases. This review summarizes the latest research advancements in these epigenetic regulatory mechanisms and therapies, providing a theoretical foundation for further elucidating the pathogenesis of kidney diseases and the development of novel therapeutic strategies.
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