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Brunetta, H.S.* ; Jung, A.S. ; Valdivieso-Rivera, F.* ; de Campos Zani, S.C.* ; Garcia Guerra, J.F. ; Furino, V.O.* ; Francisco, A.* ; Berçot, M.* ; Moraes-Vieira, P.M.M.* ; Keipert, S.* ; Jastroch, M.* ; Martinez, L.O.* ; Sponton, C.H.* ; Castilho, R.F.* ; Mori, M.A.* ; Bartelt, A.

IF1 is a cold-regulated switch of ATP synthase hydrolytic activity to support thermogenesis in brown fat.

EMBO J., DOI: 10.1038/s44318-024-00215-0 (2024)
Publ. Version/Full Text DOI PMC
Open Access Gold (Paid Option)
Creative Commons Lizenzvertrag
While mechanisms controlling uncoupling protein-1 (UCP1) in thermogenic adipocytes play a pivotal role in non-shivering thermogenesis, it remains unclear whether F1Fo-ATP synthase function is also regulated in brown adipose tissue (BAT). Here, we show that inhibitory factor 1 (IF1, encoded by Atp5if1), an inhibitor of ATP synthase hydrolytic activity, is a critical negative regulator of brown adipocyte energy metabolism. In vivo, IF1 levels are diminished in BAT of cold-adapted mice compared to controls. Additionally, the capacity of ATP synthase to generate mitochondrial membrane potential (MMP) through ATP hydrolysis (the so-called "reverse mode" of ATP synthase) is increased in brown fat. In cultured brown adipocytes, IF1 overexpression results in an inability of mitochondria to sustain the MMP upon adrenergic stimulation, leading to a quiescent-like phenotype in brown adipocytes. In mice, adeno-associated virus-mediated IF1 overexpression in BAT suppresses adrenergic-stimulated thermogenesis and decreases mitochondrial respiration in BAT. Taken together, our work identifies downregulation of IF1 upon cold as a critical event for the facilitation of the reverse mode of ATP synthase as well as to enable energetic adaptation of BAT to effectively support non-shivering thermogenesis.
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Publication type Article: Journal article
Document type Scientific Article
Corresponding Author
Keywords Adipocytes ; Metabolism ; Mitochondria ; Thermogenesis ; Ucp1; Adipose-tissue; Inhibitory Factor-1; Mitochondria; Protein; Bioenergetics; F-1-atpase; Evolution; Ucp1
ISSN (print) / ISBN 0261-4189
e-ISSN 1460-2075
Publisher Wiley
Publishing Place Heidelberg, Germany
Non-patent literature Publications
Reviewing status Peer reviewed
Grants ERC
Fundacao de Amparo a Pesquisa do Estado de Sao Paulo - FAPESP
Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior - Brasil (CAPES)
Deutsche Forschungsgemeinschaft
Deutsches Zentrum fuer Herz-Kreislauf-Forschung DZHK
Projekt DEAL