B cell tolerance to deiminated histones in BALB/c,C57BL/6, and autoimmune-prone mouse strains

Nishant Dwivedi, Annica Hedberg, Ying Yi Zheng, Indira Neeli, Minoru Satoh, Laurence Morel, Ole Petter Rekvig, Marko Radic

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Abstract

Deimination, a posttranslational modification of arginine to citrulline carried out by peptidylarginine deiminases, may compromise tolerance of self-antigens. Patients with connective tissue autoimmunity, particularly rheumatoid arthritis (RA), systemic lupus erythematosus (SLE), or Felty's syndrome, present with autoantibodies to deiminated histones (dH), which thus form a category of antibodies to citrullinated protein antigens (ACPA). In general, ACPA are a sensitive diagnostic for RA and may form in response to the release of nuclear chromatin (DNA plus dH) from granulocytes, usually referred to as neutrophil extracellular traps. The aim of this study was to examine spontaneously autoimmune mice for autoantibodies and T cell responses to dH. We compared IgG binding to deiminated and non-deiminated histones (nH) by ELISA and Western blotting in spontaneously autoimmune strains of (NZB × NZW) F1 and NZM2410 together with their derivative congenic strains, C57BL/6.Sle1 and C57BL/6.Sle1.Sle3, which display profound autoreactivity against nuclear self-antigens. The splenocyte proliferation against the two antigens was determined in the spontaneously autoimmune (NZB × NZW) F1 strain from which other autoimmune strains used in the study were derived. Immunizations with dH and nH were attempted in BALB/c mice to assess their splenocyte response. Splenocytes from BALB/c mice and from autoimmune mice at the time of conversion to autoimmunity proliferated strongly in response to dH, yet serum IgG from autoimmune (NZB × NZW) F1, NZM2410, and C57BL/6.Sle1.Sle3 mice displayed a remarkable bias against binding to dH. At the time of seroconversion, the antibodies already exhibited preference for nH, and only nH were recovered from circulating immune complexes. Analysis of histone deimination showed constitutive deimination in thymic extracts from C57BL/6 and C57BL/6.Sle1.Sle2.Sle3 triply congenic mice and in spleens of autoimmune triply congenic mice. Our study demonstrates that tolerance mechanisms against dH are intact in BALB/c and C57BL/6 mice and continue to be effective in mice with overt autoimmunity to nH. We conclude that, in contrast to human RA and SLE patients, where we frequently observe autoantibodies against dH, autoimmune mice maintain strong tolerance mechanisms to prevent the development of autoantibodies to dH.

Original languageEnglish (US)
Article number362
JournalFrontiers in immunology
Volume8
Issue numberMAR
DOIs
StatePublished - Mar 30 2017

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Histones
B-Lymphocytes
Autoantibodies
Autoimmunity
Congenic Mice
Rheumatoid Arthritis
Autoantigens
Antigens
Systemic Lupus Erythematosus
Antibodies
Immunoglobulin G
Felty Syndrome
Citrulline
Nuclear Antigens
Post Translational Protein Processing
Antigen-Antibody Complex
Inbred C57BL Mouse
Granulocytes
Connective Tissue
Chromatin

All Science Journal Classification (ASJC) codes

  • Immunology and Allergy
  • Immunology

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B cell tolerance to deiminated histones in BALB/c,C57BL/6, and autoimmune-prone mouse strains. / Dwivedi, Nishant; Hedberg, Annica; Zheng, Ying Yi; Neeli, Indira; Satoh, Minoru; Morel, Laurence; Rekvig, Ole Petter; Radic, Marko.

In: Frontiers in immunology, Vol. 8, No. MAR, 362, 30.03.2017.

Research output: Contribution to journalArticle

Dwivedi, Nishant ; Hedberg, Annica ; Zheng, Ying Yi ; Neeli, Indira ; Satoh, Minoru ; Morel, Laurence ; Rekvig, Ole Petter ; Radic, Marko. / B cell tolerance to deiminated histones in BALB/c,C57BL/6, and autoimmune-prone mouse strains. In: Frontiers in immunology. 2017 ; Vol. 8, No. MAR.
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AU - Neeli, Indira

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