Activated brown adipose tissue takes up large amounts of branched-chain amino acids (BCAAs), but their fate remains unclear. We provide evidence of a metabolic link between BCAA catabolism and haem biosynthesis, which supports mitochondrial function and regulates gene expression by influencing the epigenetic landscape of brown adipocytes.
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References
Yoneshiro, T. et al. BCAA catabolism in brown fat controls energy homeostasis through SLC25A44. Nature 572, 614–619 (2019). This paper reports BCAA uptake by BAT.
Verkerke, A. R. P. et al. BCAA-nitrogen flux in brown fat controls metabolic health independent of thermogenesis. Cell 187, 2359–2374 (2024). This paper shows how BAT uses BCAA-derived nitrogen.
Bornstein, M. R. et al. Comprehensive quantification of metabolic flux during acute cold stress in mice. Cell Metab. 35, 2077–2092 (2023). This paper provides a comprehensive analysis of nutrient utilization by different tissues in response to cold.
Park, G. et al. Quantitative analysis of metabolic fluxes in brown fat and skeletal muscle during thermogenesis. Nat. Metab. 5, 1204–1220 (2023). This paper provides a comprehensive analysis of nutrient utilization by different tissues in response to cold.
Galmozzi, A. et al. PGRMC2 is an intracellular haem chaperone critical for adipocyte function. Nature 576, 138–142 (2019). This paper reports the function of PGRMC2 in BAT.
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This is a summary of: Duerre, D. J. et al. Haem biosynthesis regulates BCAA catabolism and thermogenesis in brown adipose tissue. Nat. Metab. https://doi.org/10.1038/s42255-025-01253-6 (2025).
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A BCAA–haem axis regulates brown fat function. Nat Metab 7, 873–874 (2025). https://doi.org/10.1038/s42255-025-01266-1
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DOI: https://doi.org/10.1038/s42255-025-01266-1