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The Interaction Between Ferroptosis and Necroptosis in Acute and Chronic Kidney Diseases
Chenwen Song1,2, Fei Chen1,2, Yi Fang3
1Department of Nephrology, First Medical Center of Chinese PLA General Hospital, State Key Laboratory of Kidney Diseases, National Clinical Research Center for Kidney Diseases, Beijing Key Laboratory of Medical Devices and Integrated Traditional Chinese and Western Drug Development for Severe Kidney Diseases, Beijing, 100853, People's Republic of China.
Abstract:
Kidney disease represents a major non-communicable disease characterized by complex pathogenesis and limited therapeutic options. Current research has revealed multiple underlying mechanisms, including ferroptosis and necroptosis, which play important roles in acute kidney injury (AKI) and chronic kidney disease (CKD). Ferroptosis is an iron-dependent form of programmed cell death caused by the accumulation of lipid reactive oxygen species and is characterized by iron ion aggregation, lipid peroxidation, and excessive oxidative stress. Necroptosis is a regulated form of necrosis mediated by RIPK1-RIPK3 and is characterized by the recruitment and phosphorylation of the pseudokinase mixed lineage kinase domain-like protein (MLKL). Ferroptosis and necroptosis play important roles in various diseases such as tissue injury, cancer, and neurodegenerative diseases. Due to the intricate architecture of the kidney, the convergence of multiple systemic pathogenic factors, and the interactive regulation of intercellular signaling pathways, renal diseases exhibit complex pathogenesis and present limited therapeutic interventions. Exploring cell death and the interactions between different forms of cell death is highly important for understanding the occurrence and development of kidney diseases and for finding new treatment strategies. Ferroptosis and necroptosis influence renal cell viability and contribute to the exacerbation of kidney injury via inflammatory responses and additional mechanisms. They share common initiating factors and intersecting signaling pathways in the context of kidney diseases, thereby synergistically intensifying the pathological progression of renal damage. This article describes the pathogenesis and pathophysiological roles of ferroptosis, necroptosis, and their interactions in kidney diseases such as AKI and CKD and elucidates the potential of inhibiting ferroptosis and necroptosis, or their combined inhibition, in the prevention and treatment of kidney diseases such as AKI and CKD.
Insights
Ferroptosis and necroptosis, two cell death types, drive kidney disease progression. Targeting these pathways, individually or together, may offer new treatments for acute kidney injury and chronic kidney disease.
Area of Science:
- Cellular Biology
- Pathophysiology
- Nephrology
Background:
- Kidney disease pathogenesis is complex with limited treatments.
- Ferroptosis (iron-dependent cell death) and necroptosis (regulated necrosis) are key mechanisms in kidney injury.
- Understanding cell death interactions is crucial for novel therapeutic strategies.
Purpose of the Study:
- To explore the roles of ferroptosis and necroptosis in kidney diseases.
- To investigate the interactions between ferroptosis and necroptosis in renal pathogenesis.
- To elucidate the therapeutic potential of inhibiting these cell death pathways in kidney disease.
Main Methods:
- Literature review on ferroptosis and necroptosis in kidney disease.
- Analysis of molecular mechanisms and signaling pathways involved.
- Examination of existing and potential therapeutic interventions targeting cell death.
Main Results:
- Ferroptosis and necroptosis significantly impact renal cell viability and injury exacerbation.
- These cell death pathways share common triggers and signaling in kidney diseases.
- Their combined action synergistically worsens kidney damage.
Conclusions:
- Ferroptosis and necroptosis are critical players in acute kidney injury (AKI) and chronic kidney disease (CKD) pathogenesis.
- Targeting ferroptosis and necroptosis, alone or in combination, presents a promising therapeutic avenue for kidney diseases.
- Further research into these cell death pathways could revolutionize kidney disease treatment.
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