Up-regulated p75NTR neurotrophin receptor on glial cells in MS plaques

Neurology. 1999 Nov 10;53(8):1676-82. doi: 10.1212/wnl.53.8.1676.

Abstract

Objective: To investigate the expression of the neurotrophin receptor p75NTR on glial cells within MS plaques.

Background: In recent studies on the pathogenesis of MS white matter plaques, we found large populations of inflammatory and resident glial cells, including oligodendrocytes undergoing cell death, and identified increased expression of Fas receptor and ligand death pathway signaling molecules on the same glial cell types. In another study, the p75NTR was shown to induce apoptotic death of maturing oligodendrocytes when exposed to NGF in vitro.

Methods: We used immunohistochemistry and in situ reverse-transcription PCR to detect p75NTR expression on inflammatory and resident glial cells in MS plaques and used TUNEL staining for fragmented DNA to detect cell death.

Results: Up-regulated p75NTR messenger RNA and protein were demonstrated in both oligodendrocytes and microglia/macrophages in MS plaques but not in control white matter. However, only a fraction of p75NTR expressing oligodendrocytes was also stained by TUNEL.

Conclusions: Glial cell expression of p75NTR receptor is up-regulated during MS plaque formation. The exact role of this receptor in glial cell death and/or survival in MS remains to be elucidated.

Publication types

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

MeSH terms

  • Antigens / analysis
  • Biomarkers
  • Brain / immunology
  • Brain / metabolism*
  • Brain / pathology*
  • Humans
  • In Situ Nick-End Labeling
  • Multiple Sclerosis / immunology
  • Multiple Sclerosis / metabolism*
  • Multiple Sclerosis / pathology*
  • Neuroglia / immunology
  • Neuroglia / metabolism*
  • Oligodendroglia / metabolism
  • RNA, Messenger / metabolism
  • Receptor, Nerve Growth Factor / genetics
  • Receptor, Nerve Growth Factor / immunology
  • Receptor, Nerve Growth Factor / metabolism*
  • Up-Regulation

Substances

  • Antigens
  • Biomarkers
  • RNA, Messenger
  • Receptor, Nerve Growth Factor