Mitochondrial Carnitine/Acylcarnitine Transporter, a Novel Target of Mercury Toxicity

作者：Tonazzi Annamaria; Giangregorio Nicola; Console Lara; Scalise Mariafrancesca; La Russa Daniele; Notaristefano Caterina; Brunelli Elvira; Barca Donatella; Indiveri Cesare^*

来源：Chemical Research in Toxicology, 2015, 28(5): 1015-1022.

DOI：10.1021/acs.chemrestox.5b00050

The effect of Hg2+ and CH3Hg+ on the mitochondrial carnitine/acylcarnitine transporter (CACT) has been studied on the recombinant protein and on the CACT extracted from HeLa cells or Zebrafish and reconstituted in proteoliposomes. Transport was abolished upon treatment of the recombinant CACT in proteoliposomes by Hg2+ or CH3Hg+. Inhibition was reversed by the SH reducing agent 1,4-dithioerythritol, GSH, and N-acetylcysteine. IC50 for Hg2+ and CH3Hg+ of 90 nM and 137 nM, respectively, were measured by dose-response analyses. Inhibition was abolished in the C-less CACT mutant. Strong reduction of inhibition by both reagents was observed in the C136A and some reduction in the C155A mutants. Inhibition similar to that of the WT was observed in the C23V/C58V/C89S/C155V/C283S mutant, containing only C136. Optimal inhibition by Hg2+ was found in the four replacement mutants C23V/C58V/C89S/C283S Containing both C136 and C155 indicating cross-reaction of Hg2+ with the two Cys residues. Inhibition kinetic analysis showed mixed inhibition by Hg2+ or competitive inhibition by CH3Hg+. HeLa Cells or Zebrafish were treated with :the more potent inhibitor. Ten micromolar HgCl2 caused clear impairment of viability of HeLa cells. The transport assay in proteoliposomes with CACT extracted from treated cells showed that the transporter was inactivated and that DTE rescued the activity. Nearly identical results were observed with Zebrafish upon extraction of the CACT from the liver of the treated animals that, indeed, showed accumulation of the mercurial compound.

• 出版日期2015-5