Self DNA from lymphocytes that have undergone activation-induced cell death enhances murine B cell proliferation and antibody production

PLoS One. 2014 Oct 8;9(10):e109095. doi: 10.1371/journal.pone.0109095. eCollection 2014.

Abstract

Systemic lupus erythematosus (SLE) is characterized by prominent autoinflammatory tissue damage associated with impaired removal of dying cells and DNA. Self DNA-containing immune complexes are able to activate both innate and adaptive immune responses and play an important role in the maintenance and exacerbation of autoimmunity in SLE. In this study, we used DNA from lymphocytes that have undergone activation-induced cell death (ALD-DNA) and analyzed its role on the activation and differentiation of B cells from normal BALB/c mice as well as lupus-prone MRL+/+ and MRL/lpr mice. We found that ALD-DNA directly increased the expression of costimulatory molecules and the survival of naïve B cells in vitro. Although ALD-DNA alone had little effect on the proliferation of naïve B cells, it enhanced LPS-activated B cell proliferation in vitro and in vivo. In addition, ALD-DNA increased plasma cell numbers and IgG production in LPS-stimulated cultures of naïve B cells, in part via enhancing IL-6 production. Importantly, B cells from lupus mice were hyperresponsive to ALD-DNA and/or LPS relative to normal control B cells in terminal plasma cell differentiation, as evidenced by increases in CD138+ cell numbers, IgM production, and mRNA levels of B lymphocyte-induced maturation protein-1 (Blimp-1) and the X-box binding protein 1 (XBP1). Furthermore, ALD-DNA enhanced CD40-activated naïve B cell proliferation. Collectively, these data indicate that self DNA can serve as a DAMP (damage-associated molecular pattern) that cooperates with signals from both innate and adaptive immunity to promote polyclonal B cell activation, a common characteristic of autoimmune diseases.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibody Formation / genetics
  • Antibody Formation / physiology
  • B-Lymphocytes / metabolism*
  • DNA / metabolism
  • Deoxyribonuclease I / genetics
  • Female
  • Interleukin-6 / metabolism
  • Lupus Erythematosus, Systemic / metabolism*
  • Lymphocyte Activation / genetics
  • Lymphocyte Activation / physiology*
  • Lymphocytes / metabolism*
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred MRL lpr
  • Positive Regulatory Domain I-Binding Factor 1
  • Transcription Factors / genetics

Substances

  • Interleukin-6
  • Prdm1 protein, mouse
  • Transcription Factors
  • DNA
  • Positive Regulatory Domain I-Binding Factor 1
  • Deoxyribonuclease I

Grants and funding

The work was supported by grants from the Chinese Natural Sciences Foundation (Grant 30872337 [QL], 81273215 [YC] and 81330080 [QL]) (http://www.nsfc.gov.cn/). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.