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小鼠体内的短链和中链肉碱酰基转移酶以及酰基辅酶A硫酯酶为将β-氧化产物运出过氧化物酶体提供了互补系统。

Short- and medium-chain carnitine acyltransferases and acyl-CoA thioesterases in mouse provide complementary systems for transport of beta-oxidation products out of peroxisomes.

作者信息

Westin M A K, Hunt M C, Alexson S E H

机构信息

Karolinska Institutet, Department of Laboratory Medicine, Division of Clinical Chemistry, C1-74, Karolinska University Hospital at Huddinge, Stockholm, Sweden.

出版信息

Cell Mol Life Sci. 2008 Mar;65(6):982-90. doi: 10.1007/s00018-008-7576-6.

Abstract

Peroxisomes metabolize a variety of lipids, acting as a chain-shortening system that produces acyl-CoAs of varying chain lengths, including acetyl-CoA and propionyl-CoA. It is, however, still largely unknown how beta-oxidation products exit peroxisomes and where they are further metabolized. Peroxisomes contain carnitine acetyltransferase (CRAT) and carnitine octanoyltransferase (CROT) that produce carnitine esters for transport out of peroxisomes, together with recently characterized acyl-CoA thioesterases (ACOTs) that produce free fatty acids. Here we have performed tissue expression profiling of the short- and medium-chain carnitine acyltransferases Crat, Crot and the short- and medium-chain thioesterases (Acot12) and (Acot5), and show that they are largely expressed in different tissues, suggesting that they do not compete for the same substrates but rather provide complementary systems for transport of metabolites across the peroxisomal membrane. These data also explain earlier observed tissue differences in peroxisomal production of acetyl-CoA/acetyl-carnitine/acetate and underscores the differences in peroxisome function in various organs.

摘要

过氧化物酶体代谢多种脂质,作为一种链缩短系统,产生不同链长的酰基辅酶A,包括乙酰辅酶A和丙酰辅酶A。然而,β-氧化产物如何离开过氧化物酶体以及它们在何处进一步代谢,在很大程度上仍然未知。过氧化物酶体含有肉碱乙酰转移酶(CRAT)和肉碱辛酰转移酶(CROT),它们产生肉碱酯以便从过氧化物酶体输出,同时还有最近鉴定出的产生游离脂肪酸的酰基辅酶A硫酯酶(ACOTs)。在这里,我们对短链和中链肉碱酰基转移酶Crat、Crot以及短链和中链硫酯酶(Acot12)和(Acot5)进行了组织表达谱分析,结果表明它们在很大程度上在不同组织中表达,这表明它们并非竞争相同的底物,而是为跨过氧化物酶体膜的代谢物转运提供互补系统。这些数据也解释了早期观察到的过氧化物酶体产生乙酰辅酶A/乙酰肉碱/乙酸盐的组织差异,并强调了不同器官中过氧化物酶体功能的差异。

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