CD40-CD40L interactions induce chemokine expression by human microglia: implications for human immunodeficiency virus encephalitis and multiple sclerosis

Am J Pathol. 2002 Feb;160(2):559-67. doi: 10.1016/S0002-9440(10)64875-4.

Abstract

CD40 is a protein on microglia that is up-regulated with interferon (IFN)-gamma and is engaged by CD40L, found on CD4+ T cells, B cells, and monocytes. These interactions may be important in central nervous system inflammatory diseases. Microglia have been shown to be a source of chemokines, whose expression plays a key role in central nervous system pathologies. We examined the expression of CD40 on microglia in human immunodeficiency virus (HIV) encephalitic brain, and the effects of CD40-CD40L interactions on the expression of chemokines by cultured microglia. We found significantly increased numbers of CD40-positive microglia in HIV-infected brain tissue. Treatment of cultured microglia with IFN-gamma and CD40L increased expression of several chemokines. IFN-gamma- and CD40L-induced MCP-1 protein was mediated by activation of the ERK1/2 MAPK pathway, and Western blot analysis demonstrated phosphorylation of ERK1/2 upon stimulation of microglia. In contrast, IFN-gamma- and CD40L-induced IP-10 protein production was mediated by the p38 MAPK pathway. Our data suggest a mechanism whereby CD40L+ cells can induce microglia to secrete chemokines, amplifying inflammatory processes seen in HIV encephalitis and multiple sclerosis, and implicate CD40-CD40L interactions as a target for interventional strategies.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adolescent
  • Adult
  • Antigens, CD / immunology
  • Antigens, CD / metabolism
  • Antigens, Differentiation, Myelomonocytic / immunology
  • Antigens, Differentiation, Myelomonocytic / metabolism
  • Brain / pathology
  • Brain / physiopathology
  • CD40 Antigens / immunology
  • CD40 Antigens / metabolism*
  • CD40 Ligand / immunology
  • CD40 Ligand / metabolism*
  • CD40 Ligand / pharmacology
  • Cells, Cultured
  • Chemokines / genetics
  • Chemokines / immunology
  • Chemokines / metabolism*
  • Child
  • Encephalitis, Viral / physiopathology*
  • Female
  • HIV Infections / immunology
  • HIV Infections / physiopathology
  • Humans
  • Infant
  • Interferon-gamma / pharmacology*
  • Male
  • Microglia / drug effects*
  • Microglia / immunology
  • Microglia / metabolism
  • Middle Aged
  • Mitogen-Activated Protein Kinases / metabolism
  • Multiple Sclerosis / immunology
  • Multiple Sclerosis / physiopathology

Substances

  • Antigens, CD
  • Antigens, Differentiation, Myelomonocytic
  • CD40 Antigens
  • CD68 antigen, human
  • Chemokines
  • CD40 Ligand
  • Interferon-gamma
  • Mitogen-Activated Protein Kinases