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过氧化物酶体增殖物激活受体α对Octn2转运体(SLC22A5)的调控

Regulation of Octn2 transporter (SLC22A5) by peroxisome proliferator activated receptor alpha.

作者信息

Maeda Tomoji, Wakasawa Takeru, Funabashi Miho, Fukushi Akimasa, Fujita Masaharu, Motojima Kiyoto, Tamai Ikumi

机构信息

Department of Membrane Transport and Pharmacokinetics, Faculty of Pharmaceutical Sciences, Tokyo University of Science, Noda, Chiba, Japan.

出版信息

Biol Pharm Bull. 2008 Jun;31(6):1230-6. doi: 10.1248/bpb.31.1230.

Abstract

The tissue distribution and disposition of carnitine, which plays an important role in the transport of long-chain fatty acids across the mitochondrial inner membrane for beta-oxidation, are well controlled by carnitine transporter organic cation/carnitine transporter 2 (OCTN2). Since little information is available on regulation of the expression of the OCTN2 gene, we examined the factors that affect the expression level of rat Octn2 (rOctn2), focusing on nuclear receptor peroxisome proliferator activated receptor alpha (PPARalpha), which regulates expression of genes associated with beta-oxidation of fatty acids. mRNA of rOctn2 was induced by the PPARalpha ligand fenofibrate in primary-cultured rat hepatocytes. Further, the PPARalpha ligand Wy14643 increased the expression of Octn2 in wild-type mice, but not in PPARalpha knockout mice. Analysis of the rOctn2 promoter region suggested the presence of putative cis elements of PPARalpha. Wistar rats treated with intraperitoneal fenofibrate administration showed increased expression of rOctn2 mRNA in liver, and uptake of [3H]carnitine by freshly isolated hepatocytes derived from those rats was also increased. In conclusion, our results indicate that the nuclear receptor PPARalpha directly up-regulates the expression of rOctn2 and increases the hepatic uptake of carnitine via rOctn2.

摘要

肉碱在长链脂肪酸穿过线粒体内膜进行β-氧化的转运过程中发挥着重要作用,其组织分布和代谢由肉碱转运体有机阳离子/肉碱转运体2(OCTN2)进行良好调控。由于关于OCTN2基因表达调控的信息较少,我们研究了影响大鼠Octn2(rOctn2)表达水平的因素,重点关注调节脂肪酸β-氧化相关基因表达的核受体过氧化物酶体增殖物激活受体α(PPARα)。在原代培养的大鼠肝细胞中,rOctn2的mRNA由PPARα配体非诺贝特诱导产生。此外,PPARα配体Wy14643增加了野生型小鼠中Octn2的表达,但在PPARα基因敲除小鼠中未增加。对rOctn2启动子区域的分析表明存在PPARα的假定顺式元件。腹腔注射非诺贝特处理的Wistar大鼠肝脏中rOctn2 mRNA的表达增加,并且从这些大鼠分离的新鲜肝细胞对[3H]肉碱的摄取也增加。总之,我们的结果表明核受体PPARα直接上调rOctn2的表达,并通过rOctn2增加肝脏对肉碱的摄取。

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