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

Author:

Mohamed Bashir M1,Verma Navin K2,Davies Anthony M1,McGowan Aoife1,Crosbie-Staunton Kieran2,Prina-Mello Adriele2,Kelleher Dermot1,Botting Catherine H3,Causey Corey P4,Thompson Paul R5,Pruijn Ger JM6,Kisin Elena R7,Tkach Alexey V7,Shvedova Anna A8,Volkov Yuri9

Affiliation:

1. Department of Clinical Medicine, Trinity College Dublin, Ireland

2. Department of Clinical Medicine, Trinity College Dublin, Ireland and Centre for Research on Adaptive Nanostructures & Nanodevices, Trinity College Dublin, Ireland

3. BMS Mass Spectrometry & Proteomics Facility, University of St Andrews, Scotland, UK

4. Department of Chemistry & Biochemistry, University of South Carolina, SC, USA

5. Department of Chemistry & Biochemistry, University of South Carolina, SC, USA and Department of Chemistry, The Scripps Research Institute, FL, USA

6. Department of Biomolecular Chemistry, Radboud University Nijmegen, Nijmegen-Midden, The Netherlands

7. National Institute for Occupational Safety & Health (NIOSH), WV, USA

8. Health Effects Laboratory Division, NIOSH, Morgantown, WV, USA; National Institute for Occupational Safety & Health (NIOSH), WV, USA and Department of Pharmacology & Physiology, West Virginia University, WV, USA.

9. Department of Clinical Medicine, Trinity College Dublin, Ireland and Centre for Research on Adaptive Nanostructures & Nanodevices, Trinity College Dublin, Ireland.

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 Ca2+-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 submitted 18 March 2011; Revised submitted 10 November 2011; Published online 25 May 2012

Publisher

Future Medicine Ltd

Subject

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

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