Calcitriol increases frataxin levels and restores mitochondrial function in cell models of Friedreich Ataxia

Biochem J. 2021 Jan 15;478(1):1-20. doi: 10.1042/BCJ20200331.

Abstract

Friedreich ataxia (FA) is a neurodegenerative disease caused by the deficiency of frataxin, a mitochondrial protein. In primary cultures of dorsal root ganglia neurons, we showed that frataxin depletion resulted in decreased levels of the mitochondrial calcium exchanger NCLX, neurite degeneration and apoptotic cell death. Here, we describe that frataxin-deficient dorsal root ganglia neurons display low levels of ferredoxin 1 (FDX1), a mitochondrial Fe/S cluster-containing protein that interacts with frataxin and, interestingly, is essential for the synthesis of calcitriol, the active form of vitamin D. We provide data that calcitriol supplementation, used at nanomolar concentrations, is able to reverse the molecular and cellular markers altered in DRG neurons. Calcitriol is able to recover both FDX1 and NCLX levels and restores mitochondrial membrane potential indicating an overall mitochondrial function improvement. Accordingly, reduction in apoptotic markers and neurite degeneration was observed and, as a result, cell survival was also recovered. All these beneficial effects would be explained by the finding that calcitriol is able to increase the mature frataxin levels in both, frataxin-deficient DRG neurons and cardiomyocytes; remarkably, this increase also occurs in lymphoblastoid cell lines derived from FA patients. In conclusion, these results provide molecular bases to consider calcitriol for an easy and affordable therapeutic approach for FA patients.

Keywords: calcitriol; calcium homoeostasis; frataxin; mitochondrial dysfunction.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 25-Hydroxyvitamin D3 1-alpha-Hydroxylase / metabolism
  • Apoptosis / drug effects
  • Calcitriol / biosynthesis
  • Calcitriol / metabolism
  • Calcitriol / pharmacology*
  • Carrier Proteins / metabolism
  • Cell Line
  • Cell Survival / drug effects
  • Ferredoxins / metabolism*
  • Frataxin
  • Friedreich Ataxia / metabolism*
  • Ganglia, Spinal / cytology
  • Ganglia, Spinal / metabolism
  • Humans
  • Iron-Binding Proteins / metabolism*
  • Membrane Potential, Mitochondrial / drug effects*
  • Microfilament Proteins / metabolism
  • Mitochondria / drug effects*
  • Mitochondria / metabolism
  • Mitochondrial Proteins / metabolism
  • Myocytes, Cardiac / drug effects
  • Myocytes, Cardiac / metabolism
  • Neurons / metabolism*
  • Sodium-Calcium Exchanger / metabolism
  • Vitamin D / metabolism

Substances

  • Carrier Proteins
  • Ferredoxins
  • Iron-Binding Proteins
  • Microfilament Proteins
  • Mitochondrial Proteins
  • SLC8B1 protein, human
  • Sodium-Calcium Exchanger
  • fodrin
  • Vitamin D
  • 25-Hydroxyvitamin D3 1-alpha-Hydroxylase
  • Calcitriol