XIAP-ULK1-mediated mitophagy modulates carnitine metabolism to mitigate diabetic kidney disease

粒体自噬 生物 自噬 ULK1 肉碱 下调和上调 糖尿病 细胞生物学 肾 线粒体 内分泌学 FOXO3公司 内科学 药理学 2型糖尿病 PI3K/AKT/mTOR通路 脂质代谢 肾脏疾病 糖尿病肾病 血尿素氮
作者
Hongtu Hu,Rui Ji,Yiqun Hao,Zikang Liu,Jian Yang,Yun Cao,Qian Yang
出处
期刊:Autophagy [Taylor & Francis]
卷期号:22 (1): 207-228 被引量:5
标识
DOI:10.1080/15548627.2025.2581214
摘要

Diabetic kidney disease (DKD) is a major complication of diabetes, characterized by progressive renal dysfunction and mitochondrial impairment. Mitophagy, a selective form of macroautophagy/autophagy that maintains mitochondrial quality, is essential for kidney homeostasis. However, the molecular mechanisms by which mitophagy links these pathways to DKD remain poorly understood. This study investigated the role of XIAP-ULK1-mediated mitophagy in regulating carnitine metabolism and its therapeutic potential in alleviating DKD. Through a combination of renal biopsy analysis from DKD patients, diabetic mouse models, high-glucose-treated tubular epithelial cells, and molecular docking, we determined that XIAP upregulation led to ULK1 degradation via K48-linked polyubiquitination, impairing mitophagy and disrupting carnitine metabolism. Restoring ULK1 expression through the ULK1 agonist echinacoside and L-carnitine supplementation improved mitophagy and carnitine homeostasis, reducing kidney injury and enhancing mitochondrial function in diabetic mouse models. These findings suggested that targeting the XIAP-ULK1 axis to restore mitophagy and stabilize carnitine metabolism hold significant promise as a therapeutic strategy for DKD, highlighting the importance of metabolic regulation in kidney disease management.Abbreviations: ACR: ALB (albumin):creatinine ratio; AAV: adeno-associated virus; BUN: blood urea nitrogen; CETSA: cellular thermal shift assay; DARTS: drug affinity responsive target stability; DMEM/F12: Dulbecco’s modified Eagle medium/nutrient mixture F-12; FBS: fetal bovine serum; HG: high glucose; IHC: immunohistochemistry; IF: immunofluorescence; LC-MS: liquid chromatography-mass spectrometry; MitoQ: Mitoquinone; PCT: proximal convoluted tubule; PPI: protein-protein interaction; PAS: periodic acid-Schiff; RMSD: root mean square deviation; RMSF: root mean square fluctuation; RNA-seq: RNA sequencing; RT-qPCR: reverse transcription quantitative polymerase chain reaction; Scr: serum creatinine; SDH: succinate dehydrogenase; STZ: streptozotocin; TMLHE: trimethyllysine hydroxylase, epsilon; TEM: transmission electron microscopy; TECs: tubular epithelial cells; scRNA-seq: single-cell RNA sequencing; ULK1: unc-51 like autophagy activating kinase 1; XIAP: X-linked inhibitor of apoptosis.
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