Defective autophagy and AMPK inactivation drive ferroptosis in diabetic kidney disease.

Impaired autophagy and inactivated AMPK may increase susceptibility to ferroptosis in diabetic kidney disease, highlighting potential targets for therapeutic strategies.

Summary and findings

The study investigated the role of ferroptosis in diabetic kidney disease (DKD) by examining autophagy and AMPK signaling in proximal tubular epithelial cells (PTECs). It involved human kidney biopsy specimens and mouse models of type 1 and type 2 diabetes. The findings indicated that impaired autophagy and AMPK inactivation are associated with increased susceptibility to ferroptosis in DKD.

Abstract

<h4>Aims/hypothesis</h4>Ferroptosis, a regulated form of cell death characterised by excessive lipid peroxidation, plays a critical role in acute kidney injury (AKI). Individuals with diabetes have an elevated risk of developing AKI. However, the contribution of ferroptosis to the heightened susceptibility to AKI in diabetic kidney disease (DKD) remains unclear. This study aimed to investigate whether DKD influences ferroptosis susceptibility in proximal tubular epithelial cells (PTECs), focusing on autophagy and AMP-activated protein kinase (AMPK) signalling.<h4>Methods</h4>We examined the association between ferroptotic signatures and autophagy/AMPK pathways in human kidney biopsy specimens. To explore the roles of autophagy and AMPK in modulating ferroptosis in PTECs during DKD, we subjected streptozocin (STZ)-induced type 1 diabetic mice and type 2 diabetic db/db mice to ischaemia-reperfusion injury. Primary Atg5-deficient and wild-type PTECs were used to further investigate the underlying cellular mechanisms.<h4>Results</h4>Analysis of human kidney biopsy specimens revealed an increased ferroptotic signature (4-hydroxynonenal immunostaining), impaired autophagy (SQSTM1 accumulation) and AMPK inactivation (reduced p-AMPK) in PTECs of individuals with DKD. In STZ-treated Atg5 knockout (Atg5KO) mice, experiments combining ischaemia-reperfusion injury with ferrostatin-1 treatment showed that autophagy suppressed ferroptotic susceptibility. Additionally, susceptibility to ferroptosis was heightened in db/db mice following ischaemia-reperfusion injury; however, this effect was mitigated by enhancing autophagy through rapamycin treatment. In primary PTECs isolated from Atg5KO mice, ferroptotic cell death and lipid peroxidation were significantly increased, together with elevated mitochondrial reactive oxygen species. Mitochondrial DNA/RNA depletion substantially abolished ferroptotic effects in Atg5KO cells. Furthermore, high-glucose treatment inactivated AMPK and promoted ferroptosis, whereas treatment with the AMPK activator 5-aminoimidazole-4-carboxyamide ribonucleoside (AICAR) attenuated ferroptosis in vitro and reduced vulnerability to AKI in DKD models.<h4>Conclusions/interpretation</h4>These findings demonstrate that impaired autophagy and inactivated AMPK heighten susceptibility to ferroptosis in DKD, suggesting that therapeutic strategies targeting autophagy and AMPK activation may reduce ferroptosis-associated kidney injury in individuals with diabetes.

Limitations

Not reported in abstract.

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