» Articles » PMID: 35201595

Modes of Podocyte Death in Diabetic Kidney Disease: an Update

Overview
Journal J Nephrol
Publisher Springer
Specialty Nephrology
Date 2022 Feb 24
PMID 35201595
Authors
Affiliations
Soon will be listed here.
Abstract

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.

Citing Articles

Brown adipose tissue alleviates podocyte apoptosis through NRG4 in a male mouse model of diabetic kidney disease.

Ding S, Xu J, Tong J, Cheng Y, Shi L, Wei W Diabetologia. 2025; .

PMID: 40014139 DOI: 10.1007/s00125-025-06385-8.


Research hotspots and frontiers of endoplasmic reticulum in glomerular podocytes: a bibliometric and visual analysis from 2005 to 2023.

Junli W, Zhihong H, Lina W, Qiaoqun O, Jing Q, Jiaqi H Front Pharmacol. 2025; 15():1488340.

PMID: 39840101 PMC: 11747773. DOI: 10.3389/fphar.2024.1488340.


Focus on podocytes: diabetic kidney disease and renal fibrosis - a global bibliometric analysis (2000-2024).

An D, Tan J, Lu Y, Wen Z, Bao Y, Yao Z Front Pharmacol. 2024; 15:1454586.

PMID: 39619610 PMC: 11605685. DOI: 10.3389/fphar.2024.1454586.


Protective effect of mesenchymal stromal cells in diabetic nephropathy: the In vitro and In vivo role of the M-Sec-tunneling nanotubes.

Barutta F, Corbetta B, Bellini S, Gambino R, Bruno S, Kimura S Clin Sci (Lond). 2024; 138(23):1537-1559.

PMID: 39535903 PMC: 11609313. DOI: 10.1042/CS20242064.


N6-methyladenine RNA methylation epigenetic modification and diabetic microvascular complications.

Wang Y, Zou J, Zhou H Front Endocrinol (Lausanne). 2024; 15:1462146.

PMID: 39296713 PMC: 11408340. DOI: 10.3389/fendo.2024.1462146.


References
1.
Brosius F, Tuttle K, Kretzler M . JAK inhibition in the treatment of diabetic kidney disease. Diabetologia. 2016; 59(8):1624-7. PMC: 4942738. DOI: 10.1007/s00125-016-4021-5. View

2.
Zhou D, Zhou M, Wang Z, Fu Y, Jia M, Wang X . PGRN acts as a novel regulator of mitochondrial homeostasis by facilitating mitophagy and mitochondrial biogenesis to prevent podocyte injury in diabetic nephropathy. Cell Death Dis. 2019; 10(7):524. PMC: 6614416. DOI: 10.1038/s41419-019-1754-3. View

3.
Denhez B, Lizotte F, Guimond M, Jones N, Takano T, Geraldes P . Increased SHP-1 protein expression by high glucose levels reduces nephrin phosphorylation in podocytes. J Biol Chem. 2014; 290(1):350-8. PMC: 4281738. DOI: 10.1074/jbc.M114.612721. View

4.
Manda G, Checherita A, Comanescu M, Hinescu M . Redox Signaling in Diabetic Nephropathy: Hypertrophy versus Death Choices in Mesangial Cells and Podocytes. Mediators Inflamm. 2015; 2015:604208. PMC: 4600552. DOI: 10.1155/2015/604208. View

5.
Wang X, Liu J, Zhen J, Zhang C, Wan Q, Liu G . Histone deacetylase 4 selectively contributes to podocyte injury in diabetic nephropathy. Kidney Int. 2014; 86(4):712-25. DOI: 10.1038/ki.2014.111. View