Chair of Molecular Nutritional Medicine, TUM School of Life Sciences Weihenstephan, Technical University of Munich, Freising, Germany.
EKFZ-Else Kröner Fresenius Zentrum for Nutritional Medicine, Technical Universtiy of Munich, Freising, Germany.
Obesity (Silver Spring). 2020 Mar;28(3):590-600. doi: 10.1002/oby.22737. Epub 2020 Feb 7.
Previous studies have revealed decreased mitochondrial respiration in adipocytes of obese mice. This study aimed to identify the molecular underpinnings of altered mitochondrial metabolism in adipocytes.
Untargeted proteomics of mitochondria isolated from adipocytes and metabolite profiling of adipose tissues were conducted in diet-induced obese (DIO) and lean mice. Subcutaneous and intra-abdominal adipose tissues were studied to depict depot-specific alterations.
In subcutaneous adipocytes of DIO mice, changes in proteins related to mitochondrial structure and function were observed. Mitochondrial proteins of the inner and outer membrane were strongly reduced, whereas proteins of key matrix metabolic pathways were increased in the obese versus lean state, as further substantiated by metabolite profiling. A pronounced decrease in the oxidative phosphorylation (OXPHOS) enzymatic equipment and cristae density of the inner membrane was identified. In intra-abdominal adipocytes, similar systematic downregulation of the OXPHOS machinery in obesity occurred, but there was no regulation of outer membrane or matrix proteins.
Protein components of the OXPHOS machinery are systematically downregulated in adipose tissues of DIO mice compared with lean mice. Loss of the mitochondrial OXPHOS capacity in adipocytes may aggravate the development of metabolic disease.
先前的研究表明肥胖小鼠脂肪细胞中线粒体呼吸作用减弱。本研究旨在确定脂肪细胞中线粒体代谢改变的分子基础。
对饮食诱导肥胖(DIO)和瘦小鼠的脂肪细胞分离的线粒体进行非靶向蛋白质组学和脂肪组织代谢物分析。研究了皮下和内脏脂肪组织,以描绘特定部位的变化。
在 DIO 小鼠的皮下脂肪细胞中,观察到与线粒体结构和功能相关的蛋白质发生变化。与瘦小鼠相比,肥胖小鼠的内外膜线粒体蛋白显著减少,而关键基质代谢途径的蛋白增加,这进一步通过代谢物分析得到证实。还发现氧化磷酸化(OXPHOS)酶设备和内膜嵴密度明显下降。在腹腔脂肪细胞中,肥胖也发生了类似的 OXPHOS 机制系统性下调,但对外膜或基质蛋白没有调节。
与瘦小鼠相比,DIO 小鼠脂肪组织中线粒体 OXPHOS 机制的蛋白成分系统性地下调。脂肪细胞中线粒体 OXPHOS 能力的丧失可能会加重代谢性疾病的发展。