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<p>Diabetic kidney disease (DKD) is the leading cause of end-stage kidney disease. Tubular abnormalities may precede glomerular pathology and indicate functional progression of DKD. Here, we find glucagon injection exacerbates lipid accumulation and renal injury, in addition to causing morphological changes in proximal tubules, podocytes, and mitochondria in the early phase of DKD in mice. However, the specific knockdown or knockout of <i>Gcgr</i> in renal tubular epithelial cells almost completely halts DKD development. In contrast to the effect of short-term glucagon stimulation, long-term glucagon exposure leads to the reversal of glucagon action (glucagon reversal) in proximal tubular epithelial cells (PTECs), which is characterized by reduced energy production and an increase in lipogenesis through Gcgr-PKA-Creb-mTORC1 pathway. Accordingly, anti-GCGR antibody treatment strongly blocks the pathogenesis of DKD induced by both type 2 and type 1 diabetes. Thus, our results highlight a previously unrecognized role of glucagon/Gcgr signaling in PTEC lipogenesis and DKD.</p>

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Prolonged glucagon exposure rewires lipid oxidation and drives diabetic kidney disease progression

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2025年9月29日

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  • Xingfeng Liu,
  • Jingwen Chen,
  • Shengying Gu,
  • Yibing Chen,
  • Ruiping Zhang,
  • Qingce Zang,
  • Ting Li,
  • Hanwen Li,
  • Dejin Lu,
  • Shaocong Hou,
  • Lijuan Kong,
  • Qian Jiang,
  • Caiyi Xing,
  • Wenjia Fan,
  • Yanjun Wan,
  • Jiaqi Zhang,
  • Linyuan Zhu,
  • Chunxiao Ma,
  • Qijin Zhao,
  • Hai Yan,
  • Zeper Abliz,
  • Bing Cui,
  • Pingping Li

摘要

Diabetic kidney disease (DKD) is the leading cause of end-stage kidney disease. Tubular abnormalities may precede glomerular pathology and indicate functional progression of DKD. Here, we find glucagon injection exacerbates lipid accumulation and renal injury, in addition to causing morphological changes in proximal tubules, podocytes, and mitochondria in the early phase of DKD in mice. However, the specific knockdown or knockout of Gcgr in renal tubular epithelial cells almost completely halts DKD development. In contrast to the effect of short-term glucagon stimulation, long-term glucagon exposure leads to the reversal of glucagon action (glucagon reversal) in proximal tubular epithelial cells (PTECs), which is characterized by reduced energy production and an increase in lipogenesis through Gcgr-PKA-Creb-mTORC1 pathway. Accordingly, anti-GCGR antibody treatment strongly blocks the pathogenesis of DKD induced by both type 2 and type 1 diabetes. Thus, our results highlight a previously unrecognized role of glucagon/Gcgr signaling in PTEC lipogenesis and DKD.