Modes of podocyte death in diabetic kidney disease: an update

被引:43
作者
Jiang, Anni [1 ]
Song, Anni [1 ]
Zhang, Chun [1 ]
机构
[1] Huazhong Univ Sci & Technol, Tongji Med Coll, Dept Nephrol, Union Hosp, Jiefang Ave 1277, Wuhan 430022, Peoples R China
基金
中国国家自然科学基金;
关键词
Diabetic kidney disease; Podocyte death; Apoptosis; Autophagy; Mitotic catastrophe; ENDOPLASMIC-RETICULUM STRESS; GLUCOSE-INDUCED APOPTOSIS; MOUSE PODOCYTES; MITOTIC CATASTROPHE; EPITHELIAL-CELLS; INJURY; EXPRESSION; AUTOPHAGY; NEPHROPATHY; CONTRIBUTES;
D O I
10.1007/s40620-022-01269-1
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Diabetic kidney disease (DKD) accounts for a large proportion of end-stage renal diseases that require renal replacement therapies including dialysis and transplantation. Therefore, it is critical to understand the occurrence and development of DKD. Podocytes are mainly injured during the development of DKD, ultimately leading to their extensive death and loss. In turn, the injury and death of glomerular podocytes are also the main culprits of DKD. This review introduces the characteristics of podocytes and summarizes the modes of their death in DKD, including apoptosis, autophagy, mitotic catastrophe (MC), anoikis, necroptosis, and pyroptosis. Apoptosis is characterized by nuclear condensation and the formation of apoptotic bodies, and it exerts a different effect from autophagy in mediating DKD-induced podocyte loss. MC mediates a faulty mitotic process while anoikis separates podocytes from the basement membrane. Moreover, pyroptosis activates inflammatory factors to aggravate podocyte injuries whilst necroptosis drives signaling cascades, such as receptor-interacting protein kinases 1 and 3 and mixed lineage kinase domain-like, ultimately promoting the death of podocytes. In conclusion, a thorough knowledge of the modes of podocyte death in DKD can help us understand the development of DKD and lay the foundation for strategies in DKD disease therapy.
引用
收藏
页码:1571 / 1584
页数:14
相关论文
共 111 条
[1]   Role of albumin and its modifications in glomerular injury [J].
Agrawal, Shipra ;
Smoyer, William E. .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 2017, 469 (7-8) :975-982
[2]   Podocytes Way to Go [J].
Altintas, Mehmet M. ;
Reiser, Jochen .
AMERICAN JOURNAL OF PATHOLOGY, 2019, 189 (02) :226-228
[3]   Molecular and cellular events mediating glomerular podocyte dysfunction and depletion in diabetes mellitus [J].
Kumar, P. Anil ;
Welsh, Gavin I. ;
Saleem, Moin A. ;
Menon, Ram K. .
FRONTIERS IN ENDOCRINOLOGY, 2014, 5
[4]   Long Noncoding RNA LINC01619 Regulates MicroRNA-27a/Forkhead Box Protein O1 and Endoplasmic Reticulum Stress-Mediated Podocyte Injury in Diabetic Nephropathy [J].
Bai, Xiaoyan ;
Geng, Jian ;
Li, Xiao ;
Wan, Jiao ;
Liu, Jixing ;
Zhou, Zhanmei ;
Liu, Xiaoting .
ANTIOXIDANTS & REDOX SIGNALING, 2018, 29 (04) :355-376
[5]   JAK inhibition in the treatment of diabetic kidney disease [J].
Brosius, Frank C. ;
Tuttle, Katherine R. ;
Kretzler, Matthias .
DIABETOLOGIA, 2016, 59 (08) :1624-1627
[6]   Ursodeoxycholic acid and 4-phenylbutyrate prevent endoplasmic reticulum stress-induced podocyte apoptosis in diabetic nephropathy [J].
Cao, Ai-Li ;
Wang, Li ;
Chen, Xia ;
Wang, Yun-Man ;
Guo, Heng-Jiang ;
Chu, Shuang ;
Liu, Cheng ;
Zhang, Xue-Mei ;
Peng, Wen .
LABORATORY INVESTIGATION, 2016, 96 (06) :610-622
[7]   Role of endoplasmic reticulum stress in apoptosis of differentiated mouse podocytes induced by high glucose [J].
Cao, Yanping ;
Hao, Yongmei ;
Li, Hang ;
Liu, Qingjuan ;
Gao, Feng ;
Liu, Wei ;
Duan, Huijun .
INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE, 2014, 33 (04) :809-816
[8]   Cell death by mitotic catastrophe: a molecular definition [J].
Castedo, M ;
Perfettini, JL ;
Roumie, T ;
Andreau, K ;
Medema, R ;
Kroemer, G .
ONCOGENE, 2004, 23 (16) :2825-2837
[9]   Novel routes of albumin passage across the glomerular filtration barrier [J].
Castrop, H. ;
Schiessl, I. M. .
ACTA PHYSIOLOGICA, 2017, 219 (03) :544-553
[10]   Soluble RARRES1 induces podocyte apoptosis to promote glomerular disease progression [J].
Chen, Anqun ;
Feng, Ye ;
Lai, Han ;
Ju, Wenjun ;
Li, Zhengzhe ;
Li, Yu ;
Wang, Andrew ;
Hong, Quan ;
Zhong, Fang ;
Wei, Chengguo ;
Fu, Jia ;
Guan, Tianjun ;
Liu, Bichen ;
Kretzler, Matthias ;
Lee, Kyung ;
He, John Cijiang .
JOURNAL OF CLINICAL INVESTIGATION, 2020, 130 (10) :5523-5535