3-Hydroxyglutaric acid is transported via the sodium-dependent dicarboxylate transporter NaDC3.

  • Franziska Stellmer
  • Britta Keyser
  • Birgitta C Burckhardt
  • Hermann Koepsell
  • Thomas Streichert
  • Markus Glatzel
  • Sabrina Jabs
  • Joachim Thiem
  • Wilhelm Herdering
  • David M Koeller
  • Stephen I Goodman
  • Zoltan Lukacs
  • Kurt Ullrich
  • Gerhard Burckhardt
  • Thomas Braulke
  • Chris Mühlhausen

Abstract

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.

Bibliografische Daten

OriginalspracheDeutsch
Aufsatznummer7
ISSN0946-2716
StatusVeröffentlicht - 2007
pubmed 17356845