活性氧信号介导的热适应需要线粒体钙单转运体。

IF 5 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Suji Kim, Seung-Kuy Cha, Kyu-Sang Park, Jun Namkung
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引用次数: 0

摘要

线粒体Ca2+内流通过线粒体钙单转运体(MCU)加速线粒体生物发生和能量代谢。然而,在产热脂肪组织中,mcu依赖的线粒体激活和产热的分子机制仍然是未知的。在这项研究中,我们证明了MCU通过线粒体活性氧(mtROS)的形成来控制棕色和米色脂肪细胞的线粒体功能。棕色脂肪组织特异性Mcu敲除(Mcu BKO)小鼠表现出氧气消耗和产热减少,并伴有β-氧化和产热相关基因的下调。此外,Mcu BKO小鼠表现出mtROS减少,对冷暴露或β-肾上腺素能刺激表现出缺陷的产热反应。在Mcu BKO小鼠中,包括Ucp1在内的产热基因的下调可以通过外源ROS通过amp活化蛋白激酶(AMPK)激活来挽救。总之,我们的研究结果表明,MCU调节mtROS的形成,而mtROS反过来又介导有丝分裂核信号传导到线粒体激活的细胞反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mitochondrial Calcium Uniporter is Required for Thermogenic Adaptation Mediated by Reactive Oxygen Species Signaling.

Mitochondrial Ca2+ influx via mitochondrial calcium uniporter (MCU) accelerates mitochondrial biogenesis and energy metabolism. Nevertheless, the molecular mechanism of MCU-dependent mitochondrial activation and thermogenesis in thermogenic adipose tissues remains elusive. In this study, we demonstrate that MCU governs mitochondrial functions in brown and beige adipocytes via the formation of mitochondrial reactive oxygen species (mtROS). Mice with a brown adipose tissue-specific Mcu knockout (Mcu BKO) mice exhibited decreased oxygen consumption and heat production, accompanied by downregulation of genes related to β-oxidation and thermogenesis. Furthermore, Mcu BKO mice, exhibiting a reduction in mtROS, showed defective thermogenic responses to cold exposure or β-adrenergic stimulation. Downregulation of thermogenic genes including Ucp1 in Mcu BKO mice can be rescued by exogenous ROS through AMP-activated protein kinase (AMPK) activation. Collectively, our results suggest that MCU modulates mtROS formation, which in turn mediates mitonuclear signaling to cellular response with mitochondrial activation.

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来源期刊
Journal of Lipid Research
Journal of Lipid Research 生物-生化与分子生物学
CiteScore
11.10
自引率
4.60%
发文量
146
审稿时长
41 days
期刊介绍: The Journal of Lipid Research (JLR) publishes original articles and reviews in the broadly defined area of biological lipids. We encourage the submission of manuscripts relating to lipids, including those addressing problems in biochemistry, molecular biology, structural biology, cell biology, genetics, molecular medicine, clinical medicine and metabolism. Major criteria for acceptance of articles are new insights into mechanisms of lipid function and metabolism and/or genes regulating lipid metabolism along with sound primary experimental data. Interpretation of the data is the authors’ responsibility, and speculation should be labeled as such. Manuscripts that provide new ways of purifying, identifying and quantifying lipids are invited for the Methods section of the Journal. JLR encourages contributions from investigators in all countries, but articles must be submitted in clear and concise English.
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