Sarah Brunner, Marcus Höring, Gerhard Liebisch, Sabine Schweizer, Josef Scheiber, Piero Giansanti, Maria Hidrobo, Sven Hermeling, Josef Oeckl, Natalia Prudente de Mello, Fabiana Perocchi, Claudine Seeliger, Akim Strohmeyer, Martin Klingenspor, Johannes Plagge, Bernhard Küster, Ralph Burkhardt, Klaus-Peter Janssen, Josef Ecker
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引用次数: 0
Abstract
Lipid composition is conserved within sub-cellular compartments to maintain cell function. Lipidomic analyses of liver, muscle, white and brown adipose tissue (BAT) mitochondria revealed substantial differences in their glycerophospholipid (GPL) and free cholesterol (FC) contents. The GPL to FC ratio was 50-fold higher in brown than white adipose tissue mitochondria. Their purity was verified by comparison of proteomes with ER and mitochondria-associated membranes. A lipid signature containing PC and FC, calculated from the lipidomic profiles, allowed differentiation of mitochondria from BAT of mice housed at different temperatures. Elevating FC in BAT mitochondria prevented uncoupling protein (UCP) 1 function, whereas increasing GPL boosted it. Similarly, STARD3 overexpression facilitating mitochondrial FC import inhibited UCP1 function in primary brown adipocytes, whereas a knockdown promoted it. We conclude that the mitochondrial GPL/FC ratio is key for BAT function and propose that targeting it might be a promising strategy to promote UCP1 activity.
脂质成分在亚细胞间隙中保持不变,以维持细胞功能。对肝脏、肌肉、白色和棕色脂肪组织(BAT)线粒体进行的脂质体分析表明,它们的甘油磷脂(GPL)和游离胆固醇(FC)含量存在很大差异。棕色脂肪组织线粒体的甘油磷脂(GPL)与游离胆固醇(FC)之比是白色脂肪组织线粒体的 50 倍。通过与ER和线粒体相关膜的蛋白质组比较,验证了它们的纯度。根据脂质体图谱计算出的包含 PC 和 FC 的脂质特征,可以将不同温度下饲养的小鼠的 BAT 线粒体区分开来。提高 BAT 线粒体中的 FC 会阻止解偶联蛋白(UCP)1 的功能,而提高 GPL 则会增强其功能。同样,促进线粒体 FC 导入的 STARD3 过表达抑制了原生棕色脂肪细胞中的 UCP1 功能,而基因敲除则促进了 UCP1 功能。我们得出结论,线粒体 GPL/FC 比率是 BAT 功能的关键,并提出针对它可能是促进 UCP1 活性的一种有前途的策略。
期刊介绍:
Life Science Alliance is a global, open-access, editorially independent, and peer-reviewed journal launched by an alliance of EMBO Press, Rockefeller University Press, and Cold Spring Harbor Laboratory Press. Life Science Alliance is committed to rapid, fair, and transparent publication of valuable research from across all areas in the life sciences.