Department of Biochemistry & Cambridge Systems Biology Centre, University of Cambridge, Tennis Court Road, Cambridge CB2 1GA, U.K.
MRC, Human Nutrition Research, Elsie Widdowson Laboratory, 120 Fulbourn Road, Cambridge CB1 9NL, U.K.
J Proteome Res. 2020 Oct 2;19(10):3919-3935. doi: 10.1021/acs.jproteome.9b00894. Epub 2020 Aug 31.
Obesity is a complex disorder where the genome interacts with diet and environmental factors to ultimately influence body mass, composition, and shape. Numerous studies have investigated how bulk lipid metabolism of adipose tissue changes with obesity and, in particular, how the composition of triglycerides (TGs) changes with increased adipocyte expansion. However, reflecting the analytical challenge posed by examining non-TG lipids in extracts dominated by TGs, the glycerophospholipid composition of cell membranes has been seldom investigated. Phospholipids (PLs) contribute to a variety of cellular processes including maintaining organelle functionality, providing an optimized environment for membrane-associated proteins, and acting as pools for metabolites (e.g. choline for one-carbon metabolism and for methylation of DNA). We have conducted a comprehensive lipidomic study of white adipose tissue in mice which become obese either through genetic modification (/), diet (high fat diet), or a combination of the two, using both solid phase extraction and ion mobility to increase coverage of the lipidome. Composition changes in seven classes of lipids (free fatty acids, diglycerides, TGs, phosphatidylcholines, lyso-phosphatidylcholines, phosphatidylethanolamines, and phosphatidylserines) correlated with perturbations in one-carbon metabolism and transcriptional changes in adipose tissue. We demonstrate that changes in TGs that dominate the overall lipid composition of white adipose tissue are distinct from diet-induced alterations of PLs, the predominant components of the cell membranes. PLs correlate better with transcriptional and one-carbon metabolism changes within the cell, suggesting that the compositional changes that occur in cell membranes during adipocyte expansion have far-reaching functional consequences. Data are available at MetaboLights under the submission number: MTBLS1775.
肥胖是一种复杂的紊乱,其中基因组与饮食和环境因素相互作用,最终影响体重、组成和形状。许多研究已经调查了脂肪组织的总体脂质代谢如何随着肥胖而变化,特别是甘油三酯 (TGs) 的组成如何随着脂肪细胞的扩张而变化。然而,反映了在以 TGs 为主的提取物中检查非 TG 脂质所带来的分析挑战,细胞膜的甘油磷脂组成很少被研究。磷脂 (PLs) 有助于多种细胞过程,包括维持细胞器功能、为膜相关蛋白提供优化的环境以及作为代谢物的池 (例如胆碱用于一碳代谢和 DNA 的甲基化)。我们对肥胖的小鼠白色脂肪组织进行了全面的脂质组学研究,这些肥胖是通过遗传修饰 (/), 饮食 (高脂肪饮食) 或两者结合引起的,使用固相萃取和离子淌度来增加脂质组的覆盖范围。七种脂质类别的组成变化 (游离脂肪酸、二酰基甘油、TGs、磷脂酰胆碱、溶血磷脂酰胆碱、磷脂酰乙醇胺和磷脂酰丝氨酸) 与一碳代谢的扰动和脂肪组织中转录变化相关。我们证明,主导白色脂肪组织整体脂质组成的 TGs 的变化与 PLs 的饮食诱导改变不同,PLs 是细胞膜的主要成分。PLs 与细胞内的转录和一碳代谢变化相关性更好,表明在脂肪细胞扩张过程中发生的细胞膜组成变化具有深远的功能后果。数据可在 MetaboLights 下提交号 MTBLS1775 下查看。