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

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.

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Publication Details

Journal
Nature Communications
Published
2025-09-29
DOI
https://doi.org/10.1038/s41467-025-63529-5
Primary Topic
Diabetes Treatment and Management
Type
article
Field-Weighted Citation Impact
0.00

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article

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

Jiaqi Zhang, Shaocong Hou, Zeper Abliz, Difei Lu et al.
Nature Communications
Diabetes Treatment and Management
article

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

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

Abstract

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.

Nature CommunicationsVol. 16(1)
Chinese Academy of Medical Sciences & Peking Union Medical College (CN), International Council on Mining and Metals (GB), Molecular Discovery (United Kingdom) (GB)
Chinese Academy of Medical Sciences, Peking Union Medical College, University of California, San Diego, Bijzonder Onderzoeksfonds UGent
Openalex Percentile: Top 64%
Diabetes Treatment and Management
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