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首页> 外文期刊>Biochimica et biophysica acta. Molecular cell research >Lipid droplet remodeling and interaction with mitochondria in mouse brown adipose tissue during cold treatment
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Lipid droplet remodeling and interaction with mitochondria in mouse brown adipose tissue during cold treatment

机译:小鼠棕色脂肪组织冷处理过程中脂质液滴的重塑及其与线粒体的相互作用

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Brown adipose tissue (BAT) maintains animal body temperature by non-shivering thermogenesis, which is through uncoupling protein 1 (UCP1) that uncouples oxidative phosphorylation and utilizes beta-oxidation of fatty acids released from triacylglycerol (TAG) in lipid droplets (LDs). Increasing BAT activity and "browning" other tissues such as white adipose tissue (WAT) can enhance the expenditure of excess stored energy, and in turn reduce prevalence of metabolic diseases. Although many studies have characterized the biology of BAT and brown adipocytes, BAT LDs especially their activation induced by cold exposure remain to be explored. We have isolated LDs from mouse interscapular BAT and characterized the full proteome using mass spectrometry. Both morphological and biochemical experiments showed that the LDs could tightly associate with mitochondria. Under cold treatment mouse BAT started expressing LD structure protein PLIN-2/ADRP and increased expression of PLIN1 Both hormone sensitive lipase (HSL) and adipose TAG lipase (ATGL) were increased in LDs. In addition, isolated BAT LDs showed increased levels of the mitochondrial protein UCP1, and prolonged cold exposure could stimulate BAT mitochondrial cristae biogenesis. These changes were in agreement with the data from transcriptional analysis. Our results provide the BAT LD proteome for the first time and show that BAT LDs facilitate heat production by coupling increasing TAG hydrolysis through recruitment of ATGL and HSL to the organelle and expression of another LD resident protein PLIN2/ADRP, as well as by tightly associating with activated mitochondria. These findings will benefit the study of BAT activation and the interaction between LDs and mitochondria. (C) 2015 Elsevier B.V. All rights reserved.
机译:棕色脂肪组织(BAT)通过不发抖的生热作用来维持动物体温,这是通过解偶联蛋白1(UCP1)来实现的,该蛋白解耦了氧化磷酸化作用,并利用了脂滴(LDs)中三酰基甘油(TAG)释放的脂肪酸的β-氧化作用。提高BAT活性并“变褐”其他组织(例如白色脂肪组织(WAT))可以增加多余能量的消耗,进而降低代谢性疾病的患病率。尽管许多研究已经对BAT和棕色脂肪细胞的生物学特性进行了描述,但BAT LDs,尤其是冷暴露诱导的激活仍有待探索。我们从小鼠肩cap骨BAT中分离了LD,并使用质谱对整个蛋白质组进行了表征。形态学和生化实验均表明,LDs可以与线粒体紧密结合。在冷处理下,小鼠BAT开始表达LD结构蛋白PLIN-2 / ADRP并增加PLIN1的表达LDs中激素敏感性脂肪酶(HSL)和脂肪TAG脂肪酶(ATGL)均增加。此外,分离的BAT LDs显示线粒体蛋白UCP1水平升高,长时间的冷暴露可刺激BAT线粒体的ista生物发生。这些变化与转录分析的数据一致。我们的结果首次提供了BAT LD蛋白质组,表明BAT LDs通过将ATGL和HSL募集到细胞器和表达另一种LD驻留蛋白PLIN2 / ADRP以及紧密结合来增强TAG水解,从而促进热量产生。激活线粒体。这些发现将有利于BAT激活以及LD与线粒体之间相互作用的研究。 (C)2015 Elsevier B.V.保留所有权利。

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