Department of Clinical Chemistry, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
J Lipid Res. 2012 Jul;53(7):1296-303. doi: 10.1194/jlr.M024463. Epub 2012 Apr 25.
L-bifunctional enzyme (Ehhadh) is part of the classical peroxisomal fatty acid β-oxidation pathway. This pathway is highly inducible via peroxisome proliferator-activated receptor α (PPARα) activation. However, no specific substrates or functions for Ehhadh are known, and Ehhadh knockout (KO) mice display no appreciable changes in lipid metabolism. To investigate Ehhadh functions, we used a bioinformatics approach and found that Ehhadh expression covaries with genes involved in the tricarboxylic acid cycle and in mitochondrial and peroxisomal fatty acid oxidation. Based on these findings and the regulation of Ehhadh's expression by PPARα, we hypothesized that the phenotype of Ehhadh KO mice would become apparent after fasting. Ehhadh mice tolerated fasting well but displayed a marked deficiency in the fasting-induced production of the medium-chain dicarboxylic acids adipic and suberic acid and of the carnitine esters thereof. The decreased levels of adipic and suberic acid were not due to a deficient induction of ω-oxidation upon fasting, as Cyp4a10 protein levels increased in wild-type and Ehhadh KO mice.We conclude that Ehhadh is indispensable for the production of medium-chain dicarboxylic acids, providing an explanation for the coordinated induction of mitochondrial and peroxisomal oxidative pathways during fasting.
L-双功能酶 (Ehhadh) 是经典过氧化物酶体脂肪酸β-氧化途径的一部分。该途径可通过过氧化物酶体增殖物激活受体α (PPARα) 激活高度诱导。然而,Ehhadh 的具体底物或功能尚不清楚,Ehhadh 敲除 (KO) 小鼠的脂质代谢没有明显变化。为了研究 Ehhadh 的功能,我们使用了一种生物信息学方法,发现 Ehhadh 的表达与参与三羧酸循环以及线粒体和过氧化物酶体脂肪酸氧化的基因相关。基于这些发现以及 PPARα 对 Ehhadh 表达的调节,我们假设 Ehhadh KO 小鼠的表型在禁食后会变得明显。Ehhadh 小鼠能很好地耐受禁食,但在禁食诱导的中链二羧酸(己二酸和辛二酸)及其肉碱酯的产生中表现出明显的缺乏。己二酸和辛二酸水平的降低不是由于禁食时ω-氧化的诱导不足,因为 Cyp4a10 蛋白水平在野生型和 Ehhadh KO 小鼠中均增加。我们得出结论,Ehhadh 对于中链二羧酸的产生是必不可少的,为禁食期间线粒体和过氧化物酶体氧化途径的协调诱导提供了一个解释。