Glycerol-3-phosphate activates ChREBP, FGF21 transcription and lipogenesis in citrin deficiency

Citrin deficiency (CD) is caused by the inactivation of SLC25A13, a mitochondrial membrane protein required to move electrons from cytosolic NADH to the mitochondrial matrix in hepatocytes. People with CD do not like sweets. Here we show that SLC25A13 loss causes the accumulation of glycerol-3-phosphate (G3P), which activates the carbohydrate response element-binding protein (ChREBP) to transcribe FGF21, which acts in the brain to restrain intake of sweets and alcohol and to transcribe key genes driving lipogenesis. Mouse and human data suggest that G3P-ChREBP is a mechanistic component of the Randle Cycle that contributes to metabolic-dysfunction-associated steatotic liver disease and forms part of a system that communicates metabolic states from the liver to the brain in a manner that alters food and alcohol choices. The data provide a framework for understanding FGF21 induction in varied conditions, suggest ways to develop FGF21-inducing drugs and suggest potential drug candidates for lean metabolic-dysfunction-associated steatotic liver disease and support of urea cycle function in CD.

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Publication Details

Journal
Nature Metabolism
Published
2025-11-14
DOI
https://doi.org/10.1038/s42255-025-01399-3
Citations
2
Primary Topic
Cholesterol and Lipid Metabolism
Type
article
Field-Weighted Citation Impact
4.01

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article

Glycerol-3-phosphate activates ChREBP, FGF21 transcription and lipogenesis in citrin deficiency

Xiwei Wu, Andrew S. Zhang, Byungchang Jin, Vinod Tiwari et al.
2 citations
Nature Metabolism
Cholesterol and Lipid Metabolism
4.01
article

Glycerol-3-phosphate activates ChREBP, FGF21 transcription and lipogenesis in citrin deficiency

Xiwei Wu, Andrew S. Zhang, Byungchang Jin, Vinod Tiwari, Russell P. Goodman, Esperanza González, Hardik Shah, Mark A. Herman, Cassandra Nichole Spracklen, Min-Hsuan Chen, Olivia Sun, Charles Brenner
article en
2 citations

Abstract

Citrin deficiency (CD) is caused by the inactivation of SLC25A13, a mitochondrial membrane protein required to move electrons from cytosolic NADH to the mitochondrial matrix in hepatocytes. People with CD do not like sweets. Here we show that SLC25A13 loss causes the accumulation of glycerol-3-phosphate (G3P), which activates the carbohydrate response element-binding protein (ChREBP) to transcribe FGF21, which acts in the brain to restrain intake of sweets and alcohol and to transcribe key genes driving lipogenesis. Mouse and human data suggest that G3P-ChREBP is a mechanistic component of the Randle Cycle that contributes to metabolic-dysfunction-associated steatotic liver disease and forms part of a system that communicates metabolic states from the liver to the brain in a manner that alters food and alcohol choices. The data provide a framework for understanding FGF21 induction in varied conditions, suggest ways to develop FGF21-inducing drugs and suggest potential drug candidates for lean metabolic-dysfunction-associated steatotic liver disease and support of urea cycle function in CD.

Nature MetabolismVol. 7(11)
City Of Hope National Medical Center (US), Baylor College of Medicine (US), University of Massachusetts Amherst (US), University of Chicago (US), Massachusetts General Hospital (US), City of Hope (US), Beckman Research Institute
American Diabetes Association, California Institute of Technology, Citrin Foundation, National Institutes of Health
Openalex Percentile: Top 6%
Cholesterol and Lipid Metabolism
4.01
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