bioRxivCell BiologyPreprint
IF1 is a cold-regulated switch of ATP synthase to support thermogenesis in brown fat
H. S. Brunetta, A. S. Jung, F. B. Valdivieso-Rivera, S. C. C. Zani, V. Furino, A. Francisco, P. M. M. Moraes-Vieira, S. Keipert, M. Jastroch, L. O. Martinez, C. H. Sponton, R. F. Castilho, M. A. Mori, A. Bartelt
Abstract
While mechanisms controlling mitochondrial uncoupling protein-1 (UCP1) expression and function in thermogenic adipocytes play a pivotal role in non-shivering thermogenesis (NST), it remains unclear whether F1Fo-ATP synthase function is regulated during NST. 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 mice, IF1 protein content is markedly diminished in brown adipose tissue (BAT) after 5 days of cold exposure. Additionally, the capacity of ATP synthase to generate mitochondrial membrane potential through ATP hydrolysis (the so-called "reverse mode" of ATP synthase) is higher in mitochondria isolated from cold- adapted mice compared to mice housed at room temperature. In vitro, IF1 overexpression results in an inability of mitochondria to sustain mitochondrial membrane potential upon adrenergic stimulation and this occurs in a UCP1-dependent manner. In brown adipocytes, IF1 silencing is sufficient to increase mitochondrial lipid oxidation and the cellular dependency on glycolysis to produce ATP. Conversely, IF1 overexpression blunts mitochondrial respiration without causing cellular energetic stress, 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 this tissue. Taken together, our data shows that the downregulation of IF1 upon cold serves to facilitate the reverse mode of ATP synthase to enable energetic adaptation and effectively support NST in BAT. Graphical abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=85 SRC="FIGDIR/small/550888v2_ufig1.gif" ALT="Figure 1"> View larger version (37K): org.highwire.dtl.DTLVardef@16146faorg.highwire.dtl.DTLVardef@17afc1corg.highwire.dtl.DTLVardef@13da476org.highwire.dtl.DTLVardef@1f86fd3_HPS_FORMAT_FIGEXP M_FIG C_FIG
- organism: mouse
- assay: proteomics
- research focus: cell type annotation
- research focus: metabolism & bioenergetics
- research focus: host-pathogen & immune response
- approach: experimental assay
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Chronic cold exposure induces plasticity of mitochondrial calcium uptake in beige and brown fat of UCP1-deficient mice.
Casandra G. Chamorro, Sachin Pathuri, … Ambre M. Bertholet·bioRxiv·Mar 18, 2026
- Only a fraction of UCP1 is required to sustain adaptive nonshivering thermogenesis in the cold
Naren Qimuge, Celso Pereira Batista Sousa Filho, … Nataša Petrovič·bioRxiv·Aug 12, 2026
- White adipose tissue browning preserves UCP1-dependent nonshivering thermogenesis upon brown-adipocyte specific lipase-deficiency
Yelina Manandhar, Anita Pirchheim, … Renate Schreiber·bioRxiv·Dec 4, 2024
- Mitochondrial pyruvate carrier is required for optimal brown fat thermogenesis
V. Panic, S. Pearson, … C. Villanueva·bioRxiv·Oct 29, 2019
- Cold-inducible GOT1 activates the malate-aspartate shuttle in brown adipose tissue to support fuel preference for fatty acids
Chul‐Hong Park, Minsung Park, … Ji Suk Chang·Cell ReportsPeer-reviewed·Jun 19, 2025
- Mitochondrial Phosphatidylethanolamine Directly Regulates UCP1 to Promote Brown Adipose Thermogenesis
J. M. Johnson, A. D. Peterlin, … K. Funai·bioRxiv·Aug 26, 2022