C1q enhances IFN-gamma production by antigen-specific T cells via the CD40 costimulatory pathway on dendritic cells

Blood. 2009 Apr 9;113(15):3485-93. doi: 10.1182/blood-2008-06-164392. Epub 2009 Jan 26.

Abstract

Dendritic cells (DCs) are known to produce C1q, the initiator of the classical complement pathway. We demonstrate that murine DCs deficient in C1q (C1qa(-/-)) are poorer than wild-type (WT) DCs at eliciting the proliferation and Th1 differentiation of antigen-specific T cells. These defects result from decreased production of IL-12p70 by C1qa(-/-) DCs and impaired expression of costimulatory molecules CD80 and CD86 in response to CD40 ligation. The defective production of IL-12p70 and the reduced expression of CD80 and CD86 by C1qa(-/-) DCs were specifically mediated via CD40 ligation, as normal levels of IL-12p70 and CD80/86 were observed after ligation of Toll-like receptors (TLRs) on C1qa(-/-) DCs. CD40 ligation on C1qa(-/-) DCs, but not TLR ligation, results in decreased phosphorylation of p38 and ERK1/2 kinases. A strong colocalization of CD40 and C1q was observed by confocal microscopy upon CD40 ligation (but not TLR ligation) on DCs. Furthermore, human DCs from 2 C1q-deficient patients were found to have impaired IL-12p70 production in response to CD40L stimulation. Our novel data suggest that C1q augments the production of IL-12p70 by mouse and human DCs after CD40 triggering and plays important roles in sustaining the maturation of DCs and guiding the activation of T cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigen Presentation / immunology
  • Apoptosis / immunology
  • CD40 Antigens / metabolism*
  • Calreticulin / metabolism
  • Cell Communication / immunology
  • Cell Differentiation / immunology
  • Cells, Cultured
  • Complement C1q / genetics
  • Complement C1q / metabolism*
  • Complement C1q / pharmacology
  • Dendritic Cells / cytology
  • Dendritic Cells / drug effects
  • Dendritic Cells / metabolism*
  • Female
  • Humans
  • Interferon-gamma / metabolism*
  • Interleukin-12 / metabolism
  • Lymphocyte Transfusion
  • Male
  • Mice
  • Mice, Mutant Strains
  • Mitogen-Activated Protein Kinase 1 / metabolism
  • Mitogen-Activated Protein Kinase 3 / metabolism
  • Phagocytosis / immunology
  • Spleen / cytology
  • Th1 Cells / cytology*
  • Th1 Cells / metabolism
  • Toll-Like Receptors / metabolism
  • p38 Mitogen-Activated Protein Kinases / metabolism

Substances

  • CD40 Antigens
  • Calreticulin
  • Toll-Like Receptors
  • Interleukin-12
  • Complement C1q
  • Interferon-gamma
  • Mitogen-Activated Protein Kinase 1
  • Mitogen-Activated Protein Kinase 3
  • p38 Mitogen-Activated Protein Kinases