Stellmer Franziska, Keyser Britta, Burckhardt Birgitta C, Koepsell Hermann, Streichert Thomas, Glatzel Markus, Jabs Sabrina, Thiem Joachim, Herdering Wilhelm, Koeller David M, Goodman Stephen I, Lukacs Zoltan, Ullrich Kurt, Burckhardt Gerhard, Braulke Thomas, Mühlhausen Chris
Department of Pediatrics, University Medical Center Hamburg-Eppendorf, Martinistrasse 52, 20246, Hamburg, Germany.
J Mol Med (Berl). 2007 Jul;85(7):763-70. doi: 10.1007/s00109-007-0174-5. Epub 2007 Mar 14.
Patients with glutaryl-CoA dehydrogenase (GCDH) deficiency accumulate glutaric acid (GA) and 3-hydroxyglutaric acid (3OH-GA) in their blood and urine. To identify the transporter mediating the translocation of 3OH-GA through membranes, kidney tissue of Gcdh-/- mice have been investigated because of its central role in urinary excretion of this metabolite. Using microarray analyses of kidney-expressed genes in Gcdh-/- mice, several differentially expressed genes encoding transporter proteins were identified. Real-time polymerase chain reaction analysis confirmed the upregulation of the sodium-dependent dicarboxylate cotransporter 3 (NaDC3) and the organic cation transporter 2 (OCT2). Expression analysis of NaDC3 in Xenopus laevis oocytes by the two-electrode-voltage-clamp technique demonstrated the sodium-dependent translocation of 3OH-GA with a K (M) value of 0.95 mM. Furthermore, tracer flux measurements in Chinese hamster ovary cells overexpressing OCT2 showed that 3OH-GA inhibited significantly the uptake of methyl-4-phenylpyridinium, whereas 3OH-GA is not transported by OCT2. The data demonstrate for the first time the membrane translocation of 3OH-GA mediated by NaDC3 and the cis-inhibitory effect on OCT2-mediated transport of cations.
戊二酰辅酶A脱氢酶(GCDH)缺乏症患者的血液和尿液中会积累戊二酸(GA)和3-羟基戊二酸(3OH-GA)。为了确定介导3OH-GA跨膜转运的转运蛋白,研究了Gcdh-/-小鼠的肾脏组织,因为其在该代谢物的尿液排泄中起核心作用。通过对Gcdh-/-小鼠肾脏表达基因进行微阵列分析,鉴定出了几个编码转运蛋白的差异表达基因。实时聚合酶链反应分析证实了钠依赖性二羧酸共转运蛋白3(NaDC3)和有机阳离子转运蛋白2(OCT2)的上调。通过双电极电压钳技术对非洲爪蟾卵母细胞中的NaDC3进行表达分析,结果表明3OH-GA的钠依赖性转运,其米氏常数(K(M))值为0.95 mM。此外,在过表达OCT2的中国仓鼠卵巢细胞中的示踪剂通量测量表明,3OH-GA显著抑制了甲基-4-苯基吡啶鎓的摄取,而OCT2不转运3OH-GA。这些数据首次证明了由NaDC3介导的3OH-GA的膜转运以及对OCT2介导的阳离子转运的顺式抑制作用。