CD4-positive T cell-mediated neuroprotection requires dual compartment antigen presentation

J Neurosci. 2004 May 5;24(18):4333-9. doi: 10.1523/JNEUROSCI.5276-03.2004.

Abstract

Our laboratory discovered that CD4-positive (CD4+) T cells of the immune system convey transitory neuroprotection to injured mouse facial motoneurons (FMNs) (Serpe et al., 1999, 2000, 2003). A fundamental question in the mechanisms responsible for neuroprotection concerns the identity of the cell(s) that serves as the antigen-presenting cell (APC) to activate the CD4+ T cells. Here, we first establish that CD4+ T cells reactive to non-CNS antigen fail to support FMN survival and, second, demonstrate a two-compartment model of CD4+ T cell activation. Mouse bone marrow (BM) chimeras were developed that discriminate between resident antigen-presenting host cell and BM-derived antigen-presenting donor cell expression of major histocompatibility complex II within central and peripheral compartments, respectively. After facial nerve transection, neither compartment alone is sufficient to result in activated CD4+ T cell-mediated FMN survival. Rather, CD4+ T cell-mediated neuroprotection appears to depend on both resident microglial cells in the central compartment and a BM-derived APC in the peripheral compartment. This is the first in vivo report demonstrating a neuroprotective mechanism requiring APC functions by resident (i.e., parenchymal) microglial cells.

Publication types

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

MeSH terms

  • Animals
  • Antigen Presentation / genetics
  • Antigen Presentation / immunology*
  • Antigen-Presenting Cells / immunology
  • Antigens / immunology
  • Axotomy
  • Bone Marrow Transplantation / immunology
  • CD4-Positive T-Lymphocytes / immunology*
  • CD4-Positive T-Lymphocytes / metabolism*
  • Cell Compartmentation / genetics
  • Cell Compartmentation / immunology*
  • Cell Survival / genetics
  • Cell Survival / immunology
  • Cytoprotection / genetics
  • Cytoprotection / immunology*
  • Facial Nerve / cytology
  • Facial Nerve / physiology
  • Female
  • Genes, MHC Class II
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Microglia / cytology
  • Microglia / immunology
  • Microglia / metabolism
  • Motor Neurons / cytology
  • Motor Neurons / immunology*
  • Motor Neurons / metabolism
  • Radiation Chimera

Substances

  • Antigens