Pathogenic mechanisms underlying X-linked Charcot-Marie-Tooth neuropathy (CMTX6) in patients with a pyruvate dehydrogenase kinase 3 mutation

Neurobiol Dis. 2016 Oct:94:237-44. doi: 10.1016/j.nbd.2016.07.001. Epub 2016 Jul 5.

Abstract

Charcot-Marie-Tooth disease (CMT) is the most common inherited peripheral neuropathy. An X-linked form of CMT (CMTX6) is caused by a missense mutation (R158H) in the pyruvate dehydrogenase kinase isoenzyme 3 (PDK3) gene. PDK3 is one of 4 isoenzymes that negatively regulate the activity of the pyruvate dehydrogenase complex (PDC) by reversible phosphorylation of its first catalytic component pyruvate dehydrogenase (designated as E1). Mitochondrial PDC catalyses the oxidative decarboxylation of pyruvate to acetyl CoA and links glycolysis to the energy-producing Krebs cycle. We have previously shown the R158H mutation confers PDK3 enzyme hyperactivity. In this study we demonstrate that the increased PDK3 activity in patient fibroblasts (PDK3(R158H)) leads to the attenuation of PDC through hyper-phosphorylation of E1 at selected serine residues. This hyper-phosphorylation can be reversed by treating the PDK3(R158H) fibroblasts with the PDK inhibitor dichloroacetate (DCA). In the patient cells, down-regulation of PDC leads to increased lactate, decreased ATP and alteration of the mitochondrial network. Our findings highlight the potential to develop specific drug targeting of the mutant PDK3 as a therapeutic approach to treating CMTX6.

Keywords: Dichloroacetic acid; Mitochondria; Patient fibroblasts; Pyruvate dehydrogenase complex; Pyruvate dehydrogenase kinase 3; X-linked Charcot-Marie-Tooth neuropathy.

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Charcot-Marie-Tooth Disease / metabolism*
  • Humans
  • Isoenzymes / metabolism
  • Mitochondria / metabolism*
  • Mutation* / genetics
  • Phosphorylation
  • Protein Serine-Threonine Kinases / genetics*
  • Pyruvate Dehydrogenase Acetyl-Transferring Kinase

Substances

  • Isoenzymes
  • PDK3 protein, human
  • Pyruvate Dehydrogenase Acetyl-Transferring Kinase
  • Adenosine Triphosphate
  • Protein Serine-Threonine Kinases