Impact of fluoride and a static magnetic field on the gene expression that is associated with the antioxidant defense system of human fibroblasts

Chem Biol Interact. 2018 May 1:287:13-19. doi: 10.1016/j.cbi.2018.04.004. Epub 2018 Apr 6.

Abstract

Fluoride cytotoxicity has been associated with apoptosis, oxidative stress, general changes in DNA and RNA and protein biosynthesis, whereas the results of studies on the effect of SMF on antioxidant activity of cells are contradictory. Therefore, the aim of our study was to evaluate the simultaneous exposure of human cells to fluoride SMF that are generated by permanent magnets on the expression profile of the genes that are associated with the antioxidant defense system. Control fibroblasts and fibroblasts that had been treated with fluoride were subjected to the influence of SMF with a moderate induction. In order to achieve our aims, we applied modern molecular biology techniques such as the oligonucleotide microarray. Among the antioxidant defense genes, five (SOD1, PLK3, CLN8, XPA, HAO1), whose expression was significantly altered by the action of fluoride ions and the exposure to SMF were normalized their expression was identified. We showed that fluoride ions cause oxidative stress, whereas exposure to SMF with a moderate induction can suppress their effects by normalizing the expression of the genes that are altered by fluoride. Our research may explain the molecular mechanisms of the influence of fluoride and SMF that are generated by permanent magnets on cells.

Keywords: Antioxidant defense system; Fibroblasts; Fluoride; Oligonucleotide microarray; Static magnetic fields.

MeSH terms

  • Alcohol Oxidoreductases / genetics
  • Alcohol Oxidoreductases / metabolism
  • Antioxidants / metabolism*
  • Apoptosis / drug effects
  • Cell Line
  • Fibroblasts / cytology
  • Fibroblasts / drug effects
  • Fibroblasts / metabolism
  • Fluorides / toxicity*
  • Gene Expression / drug effects*
  • Humans
  • Magnetic Fields
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism
  • Oligonucleotide Array Sequence Analysis
  • Oxidative Stress / drug effects
  • Protein Serine-Threonine Kinases / genetics
  • Protein Serine-Threonine Kinases / metabolism
  • RNA / isolation & purification
  • RNA / metabolism
  • Reactive Oxygen Species / metabolism
  • Real-Time Polymerase Chain Reaction
  • Superoxide Dismutase / genetics
  • Superoxide Dismutase / metabolism
  • Tumor Suppressor Proteins
  • Xeroderma Pigmentosum Group A Protein / genetics
  • Xeroderma Pigmentosum Group A Protein / metabolism

Substances

  • Antioxidants
  • CLN8 protein, human
  • Membrane Proteins
  • Reactive Oxygen Species
  • Tumor Suppressor Proteins
  • XPA protein, human
  • Xeroderma Pigmentosum Group A Protein
  • RNA
  • Alcohol Oxidoreductases
  • HAO1 protein, human
  • Superoxide Dismutase
  • PLK3 protein, human
  • Protein Serine-Threonine Kinases
  • Fluorides