Published on October 28, 2025–Updated on October 28, 2025
J. Dufau, E. Recazens, L. Bottin, C. Bergoglio, A. Mairal, K. Chaoui, M.A. Marques, V. Jimenez, M. García, T. Wang, H. Laurell, J.S. Iacovoni, R. Flores-Flores, P.D. Denechaud, K. Acheikh Ibn Oumar, E. Z. Amri, C. Postic, J.P. Concordet, P. Gourdy, N. Mejhert, D. Langin (2025)
Abstract
In adipocytes, hormone-sensitive lipase (HSL) plays a key role in hydrolyzing triacylglycerols that are stored in lipid droplets. Contrary to the expected phenotype, HSL-deficient mice and humans exhibit lipodystrophy. Here, we show that HSL is also present in the adipocyte nucleus. Mouse models with different HSL subcellular localizations reveal that nuclear HSL is essential for the maintenance of adipose tissue. Gene silencing in human adipocytes shows that HSL, independently of its enzymatic activity, exerts opposing effects on mitochondrial oxidative phosphorylation and the extracellular matrix. Mechanistically, we found that HSL accumulates in the nucleus by interacting with the transforming growth factor β (TGF-β) signaling mediator, mothers against decapentaplegic homolog 3 (SMAD3). Conversely, HSL phosphorylation induces nuclear export. In vivo, HSL accumulates in the nucleus of adipocytes during high-fat feeding with the converse effect during fasting. Together, our data show that as both a cytosolic enzyme and a nuclear factor, HSL plays a pivotal role in adipocyte biology and adipose tissue maintenance.
