Sierra Ana, Subbotina Ekaterina, Zhu Zhiyong, Gao Zhan, Koganti Siva Rama Krishna, Coetzee William A, Goldhamer David J, Hodgson-Zingman Denice M, Zingman Leonid V
Department of Internal Medicine, University of Iowa, Carver College of Medicine, Iowa City, IA 52242, USA.
Department of Pediatrics, NYU School of Medicine, New York, NY 10016, USA.
Biochem Biophys Res Commun. 2016 Feb 26;471(1):129-34. doi: 10.1016/j.bbrc.2016.01.166. Epub 2016 Jan 30.
Sarcolemmal ATP-sensitive potassium (KATP) channels control skeletal muscle energy use through their ability to adjust membrane excitability and related cell functions in accordance with cellular metabolic status. Mice with disrupted skeletal muscle KATP channels exhibit reduced adipocyte size and increased fatty acid release into the circulation. As yet, the molecular mechanisms underlying this link between skeletal muscle KATP channel function and adipose mobilization have not been established. Here, we demonstrate that skeletal muscle-specific disruption of KATP channel function in transgenic (TG) mice promotes production and secretion of musclin. Musclin is a myokine with high homology to atrial natriuretic peptide (ANP) that enhances ANP signaling by competing for elimination. Augmented musclin production in TG mice is driven by a molecular cascade resulting in enhanced acetylation and nuclear exclusion of the transcription factor forkhead box O1 (FOXO1) - an inhibitor of transcription of the musclin encoding gene. Musclin production/secretion in TG is paired with increased mobilization of fatty acids and a clear trend toward increased circulating ANP, an activator of lipolysis. These data establish KATP channel-dependent musclin production as a potential mechanistic link coupling "local" skeletal muscle energy consumption with mobilization of bodily resources from fat. Understanding such mechanisms is an important step toward designing interventions to manage metabolic disorders including those related to excess body fat and associated co-morbidities.
肌膜ATP敏感性钾(KATP)通道通过根据细胞代谢状态调节膜兴奋性及相关细胞功能来控制骨骼肌能量利用。骨骼肌KATP通道功能缺失的小鼠脂肪细胞尺寸减小,且脂肪酸释放到循环中的量增加。迄今为止,骨骼肌KATP通道功能与脂肪动员之间联系的分子机制尚未明确。在此,我们证明转基因(TG)小鼠中骨骼肌特异性KATP通道功能破坏会促进肌肉素的产生和分泌。肌肉素是一种与心房利钠肽(ANP)具有高度同源性的肌动蛋白,通过竞争消除来增强ANP信号传导。TG小鼠中肌肉素产生增加是由一个分子级联驱动的,该级联导致转录因子叉头框O1(FOXO1)(肌肉素编码基因转录的抑制剂)的乙酰化增强和核排斥。TG小鼠中肌肉素的产生/分泌与脂肪酸动员增加以及循环ANP(脂解激活剂)明显增加的趋势相关。这些数据表明依赖KATP通道的肌肉素产生是将“局部”骨骼肌能量消耗与身体脂肪资源动员联系起来的潜在机制环节。理解此类机制是设计干预措施以管理包括与过多体脂及相关合并症有关的代谢紊乱的重要一步。