Wu X, Huang W, Prasad P D, Seth P, Rajan D P, Leibach F H, Chen J, Conway S J, Ganapathy V
Department of Biochemistry and Molecular Biology, Medical College of Georgia, Augusta, Georgia, USA.
J Pharmacol Exp Ther. 1999 Sep;290(3):1482-92.
We have demonstrated in the present study that novel organic cation transporter (OCTN) 2 is a transporter for organic cations as well as carnitine. OCTN2 transports organic cations without involving Na(+), but it transports carnitine only in the presence of Na(+). The ability to transport organic cations and carnitine is demonstrable with human, rat, and mouse OCTN2s. Na(+) does not influence the affinity of OCTN2 for organic cations, but it increases the affinity severalfold for carnitine. The short-chain acyl esters of carnitine are also transported by OCTN2. Two mutations, M352R and P478L, in human OCTN2 are associated with loss of transport function, but the protein expression of these mutants is comparable to that of the wild-type human OCTN2. In situ hybridization in the rat shows that OCTN2 is expressed in the proximal and distal tubules and in the glomeruli in the kidney, in the myocardium, valves, and arterioles in the heart, in the labyrinthine layer of the placenta, and in the cortex, hippocampus, and cerebellum in the brain. This is the first report that OCTN2 is a Na(+)-independent organic cation transporter as well as a Na(+)-dependent carnitine transporter and that OCTN2 is expressed not only in the heart, kidney, and placenta but also in the brain.
在本研究中,我们已证明新型有机阳离子转运体(OCTN)2是一种有机阳离子以及肉碱的转运体。OCTN2转运有机阳离子时不涉及Na⁺,但仅在有Na⁺存在时转运肉碱。人、大鼠和小鼠的OCTN2均具有转运有机阳离子和肉碱的能力。Na⁺不影响OCTN2对有机阳离子的亲和力,但会使其对肉碱的亲和力增加数倍。肉碱的短链酰基酯也可被OCTN2转运。人OCTN2中的两个突变,M352R和P478L,与转运功能丧失有关,但这些突变体的蛋白表达与野生型人OCTN2相当。大鼠原位杂交显示,OCTN2在肾脏的近端和远端小管以及肾小球、心脏的心肌、瓣膜和小动脉、胎盘的迷路层以及大脑的皮质、海马体和小脑中均有表达。这是关于OCTN2是一种不依赖Na⁺的有机阳离子转运体以及依赖Na⁺的肉碱转运体,且OCTN2不仅在心脏、肾脏和胎盘中表达,还在大脑中表达的首次报道。