Mitochondrial ATP-Sensitive K+ Channels (MitoKATP) Regulate Brown Adipocyte Differentiation and Metabolism
Osvaldo Rodrigues PereiraiD, Julian D. C. SernaiD, Camille C. Caldeira da SilvaiD, Henrique CamaraiD, Sean David KodaniiD, William T. FestucciaiD, Yu‐Hua TsengiD, Alicia Juliana KowaltowskiiD
Abstract
Brown adipose tissue (BAT) plays a central role in mammalian non-shivering thermogenesis, dissipating mitochondrial membrane potentials through the activity of uncoupling protein UCP1 to release heat. Inner membranes of mitochondria are known to be permeable to potassium ions (K+), which enter the matrix either through ATP-sensitive channels (MitoKATP) or leakage across the bilayer driven by inner membrane potentials. Mitochondrial K+ influx is associated with increased osmotic pressure, promoting water influx and increasing matrix volume. Since BAT mitochondria have lower inner membrane potentials due to uncoupling protein 1 (UCP1) activity, we hypothesized this could involve compensatory changes in MitoKATP activity, and thus tested MitoKATP involvement in brown adipocyte activities under basal and stimulated conditions. We find that cold exposure and adrenergic stimulation in mice modulate BAT MitoK levels, the channel portion of MitoKATP. Genetic ablation of the gene that codes for the pore-forming subunit of MitoKATP in human pre-adipocytes decreased cellular respiration and proliferation, compromising differentiation into mature adipocytes. In mouse cell lines, the absence of the protein limited cellular oxygen consumption in the precursor stage, but not in mature adipocytes. Interestingly, inhibition of MitoKATP in mature adipocytes increased adrenergic-stimulated oxygen consumption, indicating that shutdown of this pathway is important for full BAT thermogenesis. Similarly, MitoKATP inhibition increased oxygen consumption in BAT mitochondria isolated from mice treated with beta 3 adrenergic receptor agonist CL316,243. Overall, our results suggest that the activity of MitoKATP regulates differentiation and metabolism of brown adipocytes, impacting on thermogenesis. New and NoteworthyBrown fat cells are important to maintain healthy body weight by promoting mitochondrial uncoupling. Here, we demonstrate that mitochondrial ATP-sensitive potassium channels (MitoKATP) have important roles both in the differentiation of brown fat cells and in the activation of energy-dissipating uncoupling in this tissue.
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 0
- Organism
- Assay
- Research Focus
- Approach
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
- Mitochondrial pyruvate carrier is required for optimal brown fat thermogenesis
V. Panic, S. Pearson, … C. Villanueva·bioRxiv·Oct 29, 2019
- 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
- Orai1-mediated Ca2+ Entry Regulates Lipolysis and Mitochondrial Activation in Brown Adipose Thermogenesis
Suji Kim, Phan Anh Nguyen, … Jun Namkung·Experimental & Molecular MedicinePeer-reviewed·Aug 13, 2026
- Blocking mitochondrial pyruvate import causes energy wasting via futile lipid cycling in brown fat
M. Veliova, C. Mendes Ferreira, … O. S. Shirihai·bioRxiv·Nov 15, 2019
- NCLX prevents cell death during adrenergic activation of the brown adipose tissue
E. A. Assali, A. E. Jones, … O. S. Shirihai·bioRxiv·Nov 6, 2018
- IF1 is a cold-regulated switch of ATP synthase to support thermogenesis in brown fat
H. S. Brunetta, A. S. Jung, … A. Bartelt·bioRxiv·Jul 27, 2023