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Research progress on multiple cell death pathways of podocytes in diabetic kidney disease

期刊

MOLECULAR MEDICINE
卷 29, 期 1, 页码 -

出版社

SPRINGER
DOI: 10.1186/s10020-023-00732-4

关键词

Diabetic kidney disease; Podocyte; Apoptosis; Autophagy; Endoplasmic reticulum stress; Pyroptosis; Necroptosis; Ferroptosis; Mitotic catastrophe

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This paper discusses the pathologic research and drug therapy of diabetic kidney disease (DKD), focusing on the death processes and mechanisms of glomerular podocytes in DKD. The complexity and potential crosstalk between various modes of cell death are also examined, providing insights into podocyte death and laying the foundation for future targeted therapy strategies for DKD treatment.
Diabetic kidney disease (DKD) is the main cause of end-stage renal disease, and its clinical manifestations are progressive proteinuria, decreased glomerular filtration rate, and renal failure. The injury and death of glomerular podocytes are the keys to DKD. Currently, a variety of cell death modes have been identified in podocytes, including apoptosis, autophagy, endoplasmic reticulum (ER) stress, pyroptosis, necroptosis, ferroptosis, mitotic catastrophe, etc. The signaling pathways leading to these cell death processes are interconnected and can be activated simultaneously or in parallel. They are essential for cell survival and death that determine the fate of cells. With the deepening of the research on the mechanism of cell death, more and more researchers have devoted their attention to the underlying pathologic research and the drug therapy research of DKD. In this paper, we discussed the podocyte physiologic role and DKD processes. We also provide an overview of the types and specific mechanisms involved in each type of cell death in DKD, as well as related targeted therapy methods and drugs are reviewed. In the last part we discuss the complexity and potential crosstalk between various modes of cell death, which will help improve the understanding of podocyte death and lay a foundation for new and ideal targeted therapy strategies for DKD treatment in the future.

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