Liver proteome of mice with different genetic susceptibilities to the effects of fluoride

J Appl Oral Sci. 2016 May-Jun;24(3):250-7. doi: 10.1590/1678-775720150364.

Abstract

Objective: In this study, we investigated the differential pattern of protein expression in the liver of these mice to provide insights on why they have different responses to F.

Material and methods: Weanling male A/J and 129P3/J mice (n=10 from each strain) were pared and housed in metabolic cages with ad libitum access to low-F food and deionized water for 42 days. Liver proteome profiles were examined using nLC-MS/MS. Protein function was classified by GO biological process (Cluego v2.0.7 + Clupedia v1.0.8) and protein-protein interaction network was constructed (PSICQUIC, Cytoscape).

Results: Most proteins with fold change were increased in A/J mice. The functional category with the highest percentage of altered genes was oxidation-reduction process (20%). Subnetwork analysis revealed that proteins with fold change interacted with Disks large homolog 4 and Calcium-activated potassium channel subunit alpha-1. A/J mice had an increase in proteins related to energy flux and oxidative stress.

Conclusion: This could be a possible explanation for the high susceptibility of these mice to the effects of F, since the exposure also induces oxidative stress.

MeSH terms

  • Animals
  • Fluorides / analysis
  • Fluorides / metabolism
  • Fluorides / toxicity*
  • Fluorosis, Dental / genetics*
  • Gene Expression
  • Genetic Predisposition to Disease*
  • Liver / drug effects*
  • Liver / metabolism*
  • Male
  • Mass Spectrometry / methods
  • Mice
  • Mice, 129 Strain
  • Mice, Inbred A
  • Oxidative Stress / drug effects
  • Protein Interaction Domains and Motifs
  • Proteins / analysis*
  • Proteins / drug effects
  • Proteins / genetics
  • Proteome / drug effects*
  • Proteomics / methods
  • Reference Values
  • Time Factors

Substances

  • Proteins
  • Proteome
  • Fluorides