Stimulation of adult oligodendrogenesis by myelin-specific T cells

Am J Pathol. 2011 Oct;179(4):2028-41. doi: 10.1016/j.ajpath.2011.06.006. Epub 2011 Aug 26.

Abstract

In multiple sclerosis (MS), myelin-specific T cells are normally associated with destruction of myelin and axonal damage. However, in acute MS plaque, remyelination occurs concurrent with T-cell infiltration, which raises the question of whether T cells might stimulate myelin repair. We investigated the effect of myelin-specific T cells on oligodendrocyte formation at sites of axonal damage in the mouse hippocampal dentate gyrus. Infiltrating T cells specific for myelin proteolipid protein stimulated proliferation of chondroitin sulfate NG2-expressing oligodendrocyte precursor cells early after induction via axonal transection, resulting in a 25% increase in the numbers of oligodendrocytes. In contrast, T cells specific for ovalbumin did not stimulate the formation of new oligodendrocytes. In addition, infiltration of myelin-specific T cells enhanced the sprouting response of calretinergic associational/commissural fibers within the dentate gyrus. These results have implications for the perception of MS pathogenesis because they show that infiltrating myelin-specific T cells can stimulate oligodendrogenesis in the adult central nervous system.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aging
  • Animals
  • Axons / metabolism
  • Axons / pathology
  • Calbindin 2
  • Cell Count
  • Cell Movement
  • Cell Proliferation
  • Cytokines / genetics
  • Cytokines / metabolism
  • Dentate Gyrus / metabolism
  • Dentate Gyrus / pathology
  • Female
  • Mice
  • Myelin Proteolipid Protein / metabolism
  • Myelin Sheath / immunology*
  • Myelin Sheath / pathology*
  • Nerve Degeneration / pathology
  • Neurogenesis / immunology*
  • Neurons, Afferent / metabolism
  • Neurons, Afferent / pathology
  • Oligodendroglia / immunology*
  • Oligodendroglia / pathology*
  • Organ Specificity / immunology
  • Perforant Pathway / metabolism
  • Perforant Pathway / pathology
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • S100 Calcium Binding Protein G / metabolism
  • T-Lymphocytes / immunology*

Substances

  • Calbindin 2
  • Cytokines
  • Myelin Proteolipid Protein
  • RNA, Messenger
  • S100 Calcium Binding Protein G