Citrullination of proteins: A common post-translational modification pathway induced by different nanoparticles in vitro and in vivo

Bashir M. Mohamed, Navin K. Verma, Anthony M. Davies, Aoife McGowan, Kieran Crosbie-Staunton, Adriele Prina-Mello, Dermot Kelleher, Catherine H. Botting, Corey P. Causey, Paul R. Thompson, Ger J.M. Pruijn, Elena R. Kisin, Alexey V. Tkach, Anna A. Shvedova*, Yuri Volkov

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

85 Citations (Scopus)

Abstract

Aim: Rapidly expanding manufacture and use of nanomaterials emphasize the requirements for thorough assessment of health outcomes associated with novel applications. Post-translational protein modifications catalyzed by Ca 2+-dependent peptidylargininedeiminases have been shown to trigger immune responses including autoantibody generation, a hallmark of immune complexes deposition in rheumatoid arthritis. Therefore, the aim of the study was to assess if nanoparticles are able to promote protein citrullination. Materials & methods: Human A549 and THP-1 cells were exposed to silicon dioxide, carbon black or single-walled carbon nanotubes. C57BL/6 mice were exposed to respirable single-walled carbon nanotubes. Protein citrullination, peptidylargininedeiminases activity and target proteins were evaluated. Results: The studied nanoparticles induced protein citrullination both in cultured human cells and mouse lung tissues. Citrullination occurred via the peptidylargininedeiminase-dependent mechanism. Cytokeratines 7, 8, 18 and plectins were identified as intracellular citrullination targets. Conclusion: Nanoparticle exposure facilitated post-translational citrullination of proteins.

Original languageEnglish
Pages (from-to)1181-1195
Number of pages15
JournalNanomedicine
Volume7
Issue number8
DOIs
Publication statusPublished - Aug 2012
Externally publishedYes

ASJC Scopus Subject Areas

  • Bioengineering
  • Medicine (miscellaneous)
  • Biomedical Engineering
  • General Materials Science
  • Development

Keywords

  • autoimmunity
  • high content analysis
  • immune system
  • inflammation
  • nanomaterial
  • nanoparticle
  • peptidylargininedeiminase
  • post-translational modification
  • protein citrullination
  • rheumatoid arthritis

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