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Apoptosis-induced histone H3 methylation is targeted by autoantibodies in systemic lupus erythematosus
  1. Casandra C van Bavel1,
  2. Jürgen W Dieker1,
  3. Yvet Kroeze1,
  4. Wim P Tamboer1,
  5. Reinhard Voll2,
  6. Sylviane Muller3,
  7. Jo H Berden1,
  8. Johan van der Vlag1
  1. 1Department of Nephrology, Nephrology Research Laboratory, Nijmegen Centre for Molecular Life Sciences, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands
  2. 2Nikolaus-Fiebiger Centre of Molecular Medicine, University of Erlangen-Nuremberg, Erlangen, Germany
  3. 3CNRS, Institut de Biologie Moléculaire et Cellulaire, Strasbourg, France
  1. Correspondence to Dr J van der Vlag, Department of Nephrology, Nephrology Research Laboratory (279), Nijmegen Centre for Molecular Life Sciences, Radboud University Nijmegen Medical Centre, Geert Grooteplein 26, 6525 GA Nijmegen, The Netherlands; j.vandervlag{at}


Objectives In systemic lupus erythematosus (SLE) apoptotic chromatin is present extracellularly, which is most likely the result of disturbed apoptosis and/or insufficient removal. Released chromatin, modified during apoptosis, activates the immune system resulting in the formation of autoantibodies. A study was undertaken to identify apoptosis-induced histone modifications that play a role in SLE.

Methods The lupus-derived monoclonal antibody BT164, recently established by selection using apoptotic nucleosomes, was analysed by ELISA, western blot analysis and immunofluorescence staining using chromatin, cells, plasma and renal sections. Random peptide phage display and peptide inhibition ELISA were used to identify precisely the epitope of BT164. The reactivity of plasma samples from lupus mice and patients with SLE with the epitope of BT164 was investigated by peptide ELISA.

Results The epitope of BT164 was mapped in the N-terminal tail of histone H3 (27-KSAPAT-32) and included the apoptosis-induced trimethylation of K27. siRNA-mediated silencing of histone demethylases in cultured cells resulted in hypermethylation of H3K27 and increased nuclear reactivity of BT164. This apoptosis-induced H3K27me3 is a target for autoantibodies in patients and mice with SLE and is present in plasma and in glomerular deposits.

Conclusion In addition to previously identified acetylation of histone H4, H2A and H2B, this study shows that trimethylation of histone H3 on lysine 27 is induced by apoptosis and associated with autoimmunity in SLE. This finding is important for understanding the autoimmune response in SLE and for the development of translational strategies.

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  • Funding This work was supported by the Dutch Kidney Foundation (grant C05.2119), the Dutch Arthritis Association (grant 09-1-308) and the PhD student program of the Radboud University Nijmegen Medical Centre.

  • Competing interests None.

  • Ethics approval This study was conducted with the approval of the local ethics committee of the Radboud University Nijmegen Medical Centre.

  • Provenance and peer review Not commissioned; externally peer reviewed.

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