Mitochondrial control of fuel switching via carnitine biosynthesis

Environmental adaptation often involves a shift in energy utilization toward mitochondrial fatty acid oxidation, which requires carnitine. Besides dietary sources of animal origin, carnitine biosynthesis from trimethyllysine (TML) is essential, particularly for those who consume plant-based diets; however, its molecular regulation and physiological role remain elusive. Here, we identify SLC25A45 as a mitochondrial TML carrier that controls carnitine biosynthesis and fuel switching. SLC25A45 deficiency decreased the carnitine pool and impaired mitochondrial fatty acid oxidation, shifting reliance to carbohydrate metabolism. <i>Slc25a45</i>-deficient mice were cold-intolerant and resistant to lipid mobilization by GLP1 receptor agonist (GLP-1RA), rendering them resistant to adipose tissue loss. Our study suggests that mitochondria serve as a regulatory checkpoint in fuel switching, with implications for metabolic adaptation and the efficacy of GLP-1RA-based anti-obesity therapy.

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Publication Details

Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2025-12-18
DOI
https://doi.org/10.64898/2025.12.16.694762
Primary Topic
Metabolism and Genetic Disorders
Type
article
Field-Weighted Citation Impact
0.00
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article

Mitochondrial control of fuel switching via carnitine biosynthesis

Hiroshi Nishida, Christopher Auger, Bo Yuan, Mark Li et al.
bioRxiv (Cold Spring Harbor Laboratory)
Metabolism and Genetic Disorders
article

Mitochondrial control of fuel switching via carnitine biosynthesis

Hiroshi Nishida, Christopher Auger, Bo Yuan, Mark Li, Lijun Sun, Anthony R.P. Verkerke, Sheng Hui, Jin-Seon Yook, Jihoon Shin, Melia Granath-Panelo, Alexander S. Banks, Guilherme Martins Silva, Daisuke Katoh, Shingo Kajimura, Dandan Wang, Masanori Fujimoto, Rose Witte
article en

Abstract

Environmental adaptation often involves a shift in energy utilization toward mitochondrial fatty acid oxidation, which requires carnitine. Besides dietary sources of animal origin, carnitine biosynthesis from trimethyllysine (TML) is essential, particularly for those who consume plant-based diets; however, its molecular regulation and physiological role remain elusive. Here, we identify SLC25A45 as a mitochondrial TML carrier that controls carnitine biosynthesis and fuel switching. SLC25A45 deficiency decreased the carnitine pool and impaired mitochondrial fatty acid oxidation, shifting reliance to carbohydrate metabolism. <i>Slc25a45</i>-deficient mice were cold-intolerant and resistant to lipid mobilization by GLP1 receptor agonist (GLP-1RA), rendering them resistant to adipose tissue loss. Our study suggests that mitochondria serve as a regulatory checkpoint in fuel switching, with implications for metabolic adaptation and the efficacy of GLP-1RA-based anti-obesity therapy.

bioRxiv (Cold Spring Harbor Laboratory)
Beth Israel Deaconess Medical Center (US), Harvard University (US), University of Minnesota Medical Center (US)
Openalex Percentile: Top 57%
Metabolism and Genetic Disorders
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