线粒体atp敏感K+通道(MitoKATP)调节棕色脂肪细胞的分化和代谢。

IF 4.7 2区 生物学 Q2 CELL BIOLOGY
Osvaldo Rodrigues Pereira, Julian D C Serna, Camille C Caldeira da Silva, Henrique Camara, Sean D Kodani, William T Festuccia, Yu-Hua Tseng, Alicia J Kowaltowski
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引用次数: 0

摘要

棕色脂肪组织(BAT)在哺乳动物的非寒战产热中起着核心作用,它通过解偶联蛋白UCP1的活性消散线粒体膜电位以释放热量。已知线粒体内膜可渗透钾离子(K+),钾离子通过atp敏感通道(MitoKATP)或由内膜电位驱动的双分子层渗漏进入基质。线粒体K+内流与渗透压升高、促进水内流和增加基质体积有关。由于BAT线粒体由于解偶联蛋白1 (UCP1)活性而具有较低的内膜电位,我们假设这可能涉及MitoKATP活性的代偿性变化,因此测试了MitoKATP在基础和刺激条件下参与棕色脂肪细胞活性。我们发现小鼠的冷暴露和肾上腺素能刺激可调节MitoKATP的通道部分BAT MitoK水平。人类前脂肪细胞中编码MitoKATP成孔亚基的基因的遗传消融会降低细胞呼吸和增殖,阻碍向成熟脂肪细胞的分化。在小鼠细胞系中,该蛋白的缺失限制了前体阶段细胞的氧气消耗,但在成熟脂肪细胞中没有。有趣的是,成熟脂肪细胞中MitoKATP的抑制增加了肾上腺素能刺激的氧气消耗,表明该途径的关闭对于BAT的完全产热很重要。同样,MitoKATP抑制增加了β 3肾上腺素能受体激动剂CL316,243处理小鼠BAT线粒体的耗氧量。总之,我们的研究结果表明,MitoKATP的活性调节棕色脂肪细胞的分化和代谢,影响产热。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mitochondrial ATP-sensitive K+ channels (MitoKATP) regulate brown adipocyte differentiation and metabolism.

Brown adipose tissue (BAT) plays a central role in mammalian nonshivering 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 preadipocytes 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 the β3 adrenergic receptor agonist CL316,243. Overall, our results suggest that the activity of MitoKATP regulates differentiation and metabolism of brown adipocytes, impacting thermogenesis.NEW & NOTEWORTHY Brown fat cells are important to maintain a 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.

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来源期刊
CiteScore
9.10
自引率
1.80%
发文量
252
审稿时长
1 months
期刊介绍: The American Journal of Physiology-Cell Physiology is dedicated to innovative approaches to the study of cell and molecular physiology. Contributions that use cellular and molecular approaches to shed light on mechanisms of physiological control at higher levels of organization also appear regularly. Manuscripts dealing with the structure and function of cell membranes, contractile systems, cellular organelles, and membrane channels, transporters, and pumps are encouraged. Studies dealing with integrated regulation of cellular function, including mechanisms of signal transduction, development, gene expression, cell-to-cell interactions, and the cell physiology of pathophysiological states, are also eagerly sought. Interdisciplinary studies that apply the approaches of biochemistry, biophysics, molecular biology, morphology, and immunology to the determination of new principles in cell physiology are especially welcome.
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