Membrane translocation of glutaric acid and its derivatives

The neurodegenerative disorder glutaric aciduria type I (GA I) is characterized by increased levels of cytotoxic metabolites such as glutaric acid (GA) and 3-hydroxyglutaric (30HGA). The present report summarizes recent investigations providing insights into mechanisms of intra- and intercellular translocation of these metabolites. Initiated by microarray analyses in a mouse model of GA 1, the sodium-dependent dicarboxylate cotransporter 3 (NaC3) was the first molecule identified to mediate the translocation of GA and 30HGA with high and low affinity, respectively. More recently, organic anion transporters (OAT) I and 4 have been reported to be high-affinity transporters for GA and 30HGA as well as D-2- and L-2-hydroxyglutaric acid (D20HGA, L20HGA). The concerted action of NaC3 and OATs may be important for the directed uptake and excretion of GA, 30HGA, D20HGA and L20HGA in kidney proximal tubule cells. In addition, experimental data on cultured neuronal and glial cells isolated from mouse brain demonstrated that GA rather than 30HGA may competitively inhibit the anaplerotic supply of tricarboxylic acid cycle intermediates from astrocytes to neurons. The identification of GA and GA derivative transporters may represent targets for new approaches to treat patients with GA I and related disorders.