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Simulation of triacylglycerol ion profiles: bioinformatics for interpretation of triacylglycerol biosynthesis

机译:模拟三酰基甘油离子谱:用于解释三酰基甘油生物合成的生物信息学

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摘要

Although the synthesis pathways of intracellular triacylglycerol (TAG) species have been well elucidated, assessment of the contribution of an individual pathway to TAG pools in different mammalian organs, particularly under pathophysiological conditions, is difficult, although not impossible. Herein, we developed and validated a novel bioinformatic approach to assess the differential contributions of the known pathways to TAG pools through simulation of TAG ion profiles determined by shotgun lipidomics. This powerful approach was applied to determine such contributions in mouse heart, liver, and skeletal muscle and to examine the changes of these pathways in mouse liver induced after treatment with a high-fat diet. It was clearly demonstrated that assessment of the altered TAG biosynthesis pathways under pathophysiological conditions can be readily achieved through simulation of lipidomics data. Collectively, this new development should greatly facilitate our understanding of the biochemical mechanisms underpinning TAG accumulation at the states of obesity and lipotoxicity.
机译:尽管已经很好地阐明了细胞内三酰基甘油(TAG)种类的合成途径,但是很难评估单个途径对不同哺乳动物器官中TAG库的贡献,特别是在病理生理条件下,尽管并非不可能。在这里,我们开发并验证了一种新颖的生物信息学方法,通过模拟由shot弹枪脂质组学确定的TAG离子谱,评估已知途径对TAG池的差异贡献。这种强大的方法被用于确定在小鼠心脏,肝脏和骨骼肌中的这种贡献,并检查在用高脂饮食治疗后诱导的小鼠肝脏中这些途径的变化。清楚地表明,通过脂质组学数据的模拟,可以容易地实现在病理生理条件下改变的TAG生物合成途径的评估。总的来说,这一新进展将极大地促进我们对肥胖和脂毒性状态下TAG积累的生化机制的理解。

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