Fatty acids promote uncoupled respiration via ATP/ADP carriers in white adipocytes

Energy stored in adipocytes as triglycerides is mobilized via lipolysis, releasing fatty acids and glycerol into the circulation. Re-esterification of fatty acids that remain within the adipose tissue is the primary driver of adipocyte ATP consumption. Paradoxically, re-esterification suppresses respiration in lipolytic adipocytes. We previously found that STAT3 drives respiration by inhibiting re-esterification via GPAT3. Here we show that free fatty acids drive uncoupled respiration in complex with the ATP/ADP carriers. The impacts of lipolysis and re-esterification on uncoupled respiration correspond with fatty acids, not fatty acyl-CoAs or beta-oxidation. Under standard housing conditions, brown adipocyte uncoupling via uncoupling protein 1 is the dominant thermogenic pathway. However, in obese thermoneutral-adapted mice, uncoupled respiration in white adipocytes contributes to thermogenesis and cold tolerance, independent of brown adipose tissue or muscle activity. Our results suggest that uncoupled respiration in white adipocytes contributes to whole-body energy expenditure and could be a promising target for obesity treatment.

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Publication Details

Journal
Nature Metabolism
Published
2026-02-23
DOI
https://doi.org/10.1038/s42255-026-01467-2
Primary Topic
Adipose Tissue and Metabolism
Type
article
Field-Weighted Citation Impact
0.00

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article

Fatty acids promote uncoupled respiration via ATP/ADP carriers in white adipocytes

S. C-H. Chen, Nicolás Gómez-Banoy, Shannon M. Reilly, Oluwafemi Gbayisomore et al.
Nature Metabolism
Adipose Tissue and Metabolism
article

Fatty acids promote uncoupled respiration via ATP/ADP carriers in white adipocytes

S. C-H. Chen, Nicolás Gómez-Banoy, Shannon M. Reilly, Oluwafemi Gbayisomore, Maryam Ahmadian, Zane J. Zerbel, Yosip Kelemen, Preetveer Dhillon, A. Melisa Aksu
article en

Abstract

Energy stored in adipocytes as triglycerides is mobilized via lipolysis, releasing fatty acids and glycerol into the circulation. Re-esterification of fatty acids that remain within the adipose tissue is the primary driver of adipocyte ATP consumption. Paradoxically, re-esterification suppresses respiration in lipolytic adipocytes. We previously found that STAT3 drives respiration by inhibiting re-esterification via GPAT3. Here we show that free fatty acids drive uncoupled respiration in complex with the ATP/ADP carriers. The impacts of lipolysis and re-esterification on uncoupled respiration correspond with fatty acids, not fatty acyl-CoAs or beta-oxidation. Under standard housing conditions, brown adipocyte uncoupling via uncoupling protein 1 is the dominant thermogenic pathway. However, in obese thermoneutral-adapted mice, uncoupled respiration in white adipocytes contributes to thermogenesis and cold tolerance, independent of brown adipose tissue or muscle activity. Our results suggest that uncoupled respiration in white adipocytes contributes to whole-body energy expenditure and could be a promising target for obesity treatment.

Nature MetabolismVol. 8(3)
Memorial Sloan Kettering Cancer Center (US), Cornell University (US), University of California San Diego (US), Rockefeller University (US)
National Institutes of Health
Affordable and clean energy
Openalex Percentile: Top 45%
Adipose Tissue and Metabolism
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