The critical role of dysregulated autophagy in the progression of diabetic kidney disease

被引:8
|
作者
Zhang, Ziwei [1 ]
Sun, Yuting [2 ]
Xue, Jiaojiao [1 ]
Jin, De [3 ]
Li, Xiangyan [4 ]
Zhao, Daqing [4 ]
Lian, Fengmei [5 ]
Qi, Wenxiu [4 ]
Tong, Xiaolin [6 ]
机构
[1] Changchun Univ Chinese Med, Coll Tradit Chinese Med, Changchun, Peoples R China
[2] China Acad Chinese Med Sci, Guanganmen Hosp, Dept Endocrinol, Beijing, Peoples R China
[3] Hangzhou Hosp Tradit Chinese Med, Hangzhou, Peoples R China
[4] Changchun Univ Chinese Med, Jilin Prov Key Lab Biomacromol Chinese Med, Northeast Asia Res Inst Tradit Chinese Med, Minist Educ,Key Lab Act Subst & Biol Mech Ginseng, Changchun, Peoples R China
[5] China Acad Chinese Med Sci, Guanganmen Hosp, Beijing, Peoples R China
[6] China Acad Chinese Med Sci, Guanganmen Hosp, Inst Metab Dis, Beijing, Peoples R China
关键词
diabetic kidney disease; autophagy; autophagosome; lysosome; podocytes; renal tubular epithelial cells; ENDOPLASMIC-RETICULUM STRESS; GLYCATION END-PRODUCTS; PODOCYTE INJURY; NEPHROPATHY; PROTEIN; CELL; APOPTOSIS; MECHANISMS; AMPK; MTOR;
D O I
10.3389/fphar.2022.977410
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Diabetic kidney disease (DKD) is one of the major public health problems in society today. It is a renal complication caused by diabetes mellitus with predominantly microangiopathy and is a major cause of end-stage renal disease (ESRD). Autophagy is a metabolic pathway for the intracellular degradation of cytoplasmic products and damaged organelles and plays a vital role in maintaining homeostasis and function of the renal cells. The dysregulation of autophagy in the hyperglycaemic state of diabetes mellitus can lead to the progression of DKD, and the activation or restoration of autophagy through drugs is beneficial to the recovery of renal function. This review summarizes the physiological process of autophagy, illustrates the close link between DKD and autophagy, and discusses the effects of drugs on autophagy and the signaling pathways involved from the perspective of podocytes, renal tubular epithelial cells, and mesangial cells, in the hope that this will be useful for clinical treatment.
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收藏
页数:19
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