The emerging role of regulated cell death in ischemia and reperfusion-induced acute kidney injury: current evidence and future perspectives

被引:14
作者
Li, Chenning [1 ,2 ]
Yu, Ying [1 ,2 ]
Zhu, Shuainan [1 ,2 ]
Hu, Yan [1 ,2 ]
Ling, Xiaomin [1 ,2 ]
Xu, Liying [1 ,2 ]
Zhang, Hao [1 ,2 ]
Guo, Kefang [1 ,2 ]
机构
[1] Zhongshan Hosp, Dept Anesthesiol, Shanghai, Peoples R China
[2] Shanghai Key Lab Perioperat Stress & Protect, Shanghai, Peoples R China
基金
上海市自然科学基金;
关键词
LIVER-REGENERATION PROTECTS; NECROPTOSIS; FERROPTOSIS; PATHOPHYSIOLOGY; RECOMMENDATIONS; DEFICIENCY; PANOPTOSIS; APOPTOSIS; AUGMENTOR; PATHWAYS;
D O I
10.1038/s41420-024-01979-4
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Renal ischemia-reperfusion injury (IRI) is one of the main causes of acute kidney injury (AKI), which is a potentially life-threatening condition with a high mortality rate. IRI is a complex process involving multiple underlying mechanisms and pathways of cell injury and dysfunction. Additionally, various types of cell death have been linked to IRI, including necroptosis, apoptosis, pyroptosis, and ferroptosis. These processes operate differently and to varying degrees in different patients, but each plays a role in the various pathological conditions of AKI. Advances in understanding the underlying pathophysiology will lead to the development of new therapeutic approaches that hold promise for improving outcomes for patients with AKI. This review provides an overview of the recent research on the molecular mechanisms and pathways underlying IRI-AKI, with a focus on regulated cell death (RCD) forms such as necroptosis, pyroptosis, and ferroptosis. Overall, targeting RCD shows promise as a potential approach to treating IRI-AKI.
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页数:10
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