Following direct CD40 activation, human primary microglial cells produce IL-12 p40 but not bioactive IL-12 p70

Cytokine. 2001 Apr 21;14(2):88-96. doi: 10.1006/cyto.2000.0855.

Abstract

There is accumulating evidence that interleukin 12 (IL-12) is involved in the pathogenesis of multiple sclerosis. In the periphery, this cytokine is produced by antigen-presenting cells (APCs) following interaction with activated T cells. CD40 ligation plays a crucial role in this production. Microglial cells are thought to play a major role in antigen presentation in the central nervous system. In this work, we examined IL-12 production by human primary microglial cells after CD40 ligation. These cells expressed CD40 and MHC class II following interferon-gamma activation. IL-12 p40 mRNA and protein, but not bioactive IL-12 p70, were detected in response to direct CD40 activation. Microglial cells co-cultured with activated allogenic CD4+ T lymphocytes also produced IL-12 p40 but not IL-12 p70. This IL-12 p40 production was inhibited by anti-CD40 ligand. Altogether, these results suggest that CD40-CD40-ligand interaction provides a signal that triggers IL-12 p40 expression. However, other interaction(s) may be required during antigen presentation for bioactive heterodimeric IL-12 p70 to be produced by microglial cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • CD4 Antigens / metabolism
  • CD4-Positive T-Lymphocytes / cytology
  • CD4-Positive T-Lymphocytes / drug effects
  • CD40 Antigens / metabolism*
  • CD40 Ligand / genetics
  • CD40 Ligand / metabolism
  • Cell Line
  • Cells, Cultured
  • Central Nervous System / cytology
  • Central Nervous System / metabolism
  • Coculture Techniques
  • Enzyme-Linked Immunosorbent Assay
  • Fibroblasts
  • Flow Cytometry
  • Histocompatibility Antigens Class II / metabolism
  • Humans
  • Interferon-gamma / pharmacology
  • Interleukin-12 / chemistry*
  • Interleukin-12 / genetics
  • Interleukin-12 / metabolism*
  • Interleukin-12 / pharmacology
  • Mice
  • Microglia / drug effects
  • Microglia / metabolism*
  • Molecular Weight
  • Phytohemagglutinins / pharmacology
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism

Substances

  • CD4 Antigens
  • CD40 Antigens
  • Histocompatibility Antigens Class II
  • Phytohemagglutinins
  • RNA, Messenger
  • CD40 Ligand
  • Interleukin-12
  • Interferon-gamma