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Hormone-induced mitochondrial fission is utilized by brown adipocytes as an amplification pathway for energy expenditure

机译:激素诱导的线粒体裂变被棕色脂肪细胞用作能量消耗的放大途径

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摘要

Adrenergic stimulation of brown adipocytes (BA) induces mitochondrial uncoupling, thereby increasing energy expenditure by shifting nutrient oxidation towards thermogenesis. Here we describe that mitochondrial dynamics is a physiological regulator of adrenergically-induced changes in energy expenditure. The sympathetic neurotransmitter Norepinephrine (NE) induced complete and rapid mitochondrial fragmentation in BA, characterized by Drp1 phosphorylation and Opa1 cleavage. Mechanistically, NE-mediated Drp1 phosphorylation was dependent on Protein Kinase-A (PKA) activity, whereas Opa1 cleavage required mitochondrial depolarization mediated by FFAs released as a result of lipolysis. This change in mitochondrial architecture was observed both in primary cultures and brown adipose tissue from cold-exposed mice. Mitochondrial uncoupling induced by NE in brown adipocytes was reduced by inhibition of mitochondrial fission through transient Drp1 DN overexpression. Furthermore, forced mitochondrial fragmentation in BA through Mfn2 knock down increased the capacity of exogenous FFAs to increase energy expenditure. These results suggest that, in addition to its ability to stimulate lipolysis, NE induces energy expenditure in BA by promoting mitochondrial fragmentation. Together these data reveal that adrenergically-induced changes to mitochondrial dynamics are required for BA thermogenic activation and for the control of energy expenditure.
机译:肾上腺能刺激棕色脂肪细胞(BA)诱导线粒体解偶联,从而通过将营养物氧化转移到生热作用而增加能量消耗。在这里,我们描述线粒体动力学是肾上腺素引起的能量消耗变化的生理调节剂。交感神经递质去甲肾上腺素(NE)诱导BA中线粒体的完全和快速断裂,其特征是Drp1磷酸化和Opa1裂解。从机理上讲,NE介导的Drp1磷酸化依赖于蛋白激酶-A(PKA)活性,而Opa1切割则需要由脂解作用释放的FFA介导的线粒体去极化。在原始培养物和冷暴露小鼠的棕色脂肪组织中均观察到线粒体结构的这种变化。 NE通过短暂的Drp1 DN过表达抑制线粒体裂变而减少了棕色脂肪细胞中NE诱导的线粒体解偶联。此外,通过Mfn2敲低迫使BA中的线粒体片段化增加了外源FFA增加能量消耗的能力。这些结果表明,除了刺激脂肪分解的能力外,NE还通过促进线粒体片段化在BA中诱导能量消耗。这些数据共同表明,肾上腺素诱导的线粒体动力学变化是BA生热激活和控制能量消耗所必需的。

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