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Aims/hypothesis <p>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.</p> Methods <p>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&#xa0;1 diabetic mice and type&#xa0;2 diabetic <i>db</i>/<i>db</i> mice to ischaemia–reperfusion injury. Primary <i>Atg5</i>-deficient and wild-type PTECs were used to further investigate the underlying cellular mechanisms.</p> Results <p>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 <i>Atg5</i> knockout (Atg5KO)&#xa0;mice, experiments combining ischaemia–reperfusion injury with ferrostatin-1 treatment showed that autophagy suppressed ferroptotic susceptibility. Additionally, susceptibility to ferroptosis was heightened in <i>db</i>/<i>db</i> mice following ischaemia–reperfusion injury; however, this effect was mitigated by enhancing autophagy through rapamycin treatment. In primary PTECs isolated from Atg5KO&#xa0;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.</p> Conclusions/interpretation <p>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.</p> Graphical Abstract <p></p>

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Defective autophagy and AMPK inactivation drive ferroptosis in diabetic kidney disease

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2025年11月28日

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  • Sho Matsui,
  • Takeshi Yamamoto,
  • Yoshitsugu Takabatake,
  • Atsushi Takahashi,
  • Tomoko Namba-Hamano,
  • Jun Matsuda,
  • Satoshi Minami,
  • Shinsuke Sakai,
  • Hiroaki Yonishi,
  • Jun Nakamura,
  • Hideaki Kawai,
  • Takuya Kubota,
  • Isao Matsui,
  • Motoko Yanagita,
  • Yoshitaka Isaka

摘要

Aims/hypothesis

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.

Methods

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.

Results

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.

Conclusions/interpretation

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.

Graphical Abstract