自噬
肾
发病机制
医学
癌症研究
细胞生物学
肾干细胞
纤维化
细胞凋亡
病理
生物
内科学
干细胞
生物化学
祖细胞
作者
Xingchen Zhao,Man J. Livingston,Xinling Liang,Zheng Dong
标识
DOI:10.1007/978-981-13-8871-2_28
摘要
Renal fibrosis is the final common pathway of all chronic kidney diseases progressing to end-stage renal diseases. Autophagy, a highly conserved lysosomal degradation pathway, plays important roles in maintaining cellular homeostasis in all major types of kidney cells including renal tubular cells as well as podocytes, mesangial cells and endothelial cells in glomeruli. Autophagy dysfunction is implicated in the pathogenesis of various renal pathologies. Here, we analyze the pathological role and regulation of autophagy in renal fibrosis and related kidney diseases in both glomeruli and tubulointerstitial compartments. Further research is expected to gain significant mechanistic insights and discover pathway-specific and kidney-selective therapies targeting autophagy to prevent renal fibrosis and related kidney diseases.
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