Silver nanoparticle-induced hemoglobin decrease involves alteration of histone 3 methylation status

Biomaterials. 2015 Nov:70:12-22. doi: 10.1016/j.biomaterials.2015.08.015. Epub 2015 Aug 11.

Abstract

Silver nanoparticles (nanosilver, AgNPs) have been shown to induce toxicity in vitro and in vivo; however, the molecular bases underlying the detrimental effects have not been thoroughly understood. Although there are numerous studies on its genotoxicity, only a few studies have investigated the epigenetic changes, even less on the changes of histone modifications by AgNPs. In the current study, we probed the AgNP-induced alterations to histone methylation that could be responsible for globin reduction in erythroid cells. AgNP treatment caused a significant reduction of global methylation level for histone 3 (H3) in erythroid MEL cells at sublethal concentrations, devoid of oxidative stress. The ChIP-PCR analyses demonstrated that methylation of H3 at lysine (Lys) 4 (H3K4) and Lys 79 (H3K79) on the β-globin locus was greatly reduced. The reduction in methylation could be attributed to decreased histone methyltransferase DOT-1L and MLL levels as well as the direct binding between AgNPs to H3/H4 that provide steric hindrance to prevent methylation as predicted by the all-atom molecular dynamics simulations. This direct interaction was further proved by AgNP-mediated pull-down assay and immunoprecipitation assay. These changes, together with decreased RNA polymerase II activity and chromatin binding at this locus, resulted in decreased hemoglobin production. By contrast, Ag ion-treated cells showed no alterations in histone methylation level. Taken together, these results showed a novel finding in which AgNPs could alter the methylation status of histone. Our study therefore opens a new avenue to study the biological effects of AgNPs at sublethal concentrations from the perspective of epigenetic mechanisms.

Keywords: Epigenetics; Hemoglobin; Histone; Methylation; Nanosilver; Transcription.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line, Tumor
  • Cell Survival / drug effects
  • Genetic Loci
  • Hemoglobins
  • Histone Methyltransferases
  • Histone-Lysine N-Methyltransferase / metabolism
  • Histones / metabolism*
  • Immunoprecipitation
  • Metal Nanoparticles / chemistry*
  • Metal Nanoparticles / ultrastructure
  • Methylation / drug effects
  • Mice
  • Molecular Dynamics Simulation
  • Protein Binding / drug effects
  • Protein Multimerization / drug effects
  • Silver / pharmacology*
  • beta-Globins / metabolism

Substances

  • Hemoglobins
  • Histones
  • beta-Globins
  • Silver
  • Histone Methyltransferases
  • Histone-Lysine N-Methyltransferase