Elevated activity and microglial expression of myeloperoxidase in demyelinated cerebral cortex in multiple sclerosis

Elizabeth Gray1, Taya L Thomas, Samar Betmouni

  • 1Glial Cell Biology Laboratories, University of Bristol Institute of Clinical Neuroscience, Frenchay Hospital, Bristol, UK.

Insights

In multiple sclerosis (MS), activated microglia expressing myeloperoxidase (MPO) are linked to gray matter demyelination. This suggests microglial reactive oxygen species contribute to cortical damage in MS patients.

Area of Science:

  • Neuroscience
  • Immunology
  • Pathology

Background:

  • Progressive multiple sclerosis (MS) involves extensive cortical demyelination.
  • Gray matter demyelination in MS is associated with microglial activation.
  • Macrophages and microglia express myeloperoxidase (MPO) and generate reactive oxygen species (ROS) during myelin phagocytosis.

Purpose of the Study:

  • To investigate microglial activation in the cerebral cortex of MS patients.
  • To determine the relationship between microglial activation, MPO activity, and cortical demyelination in MS.

Main Methods:

  • Analysis of 34 cortical lesions from 21 neuropathologically confirmed MS cases.
  • Immunohistochemistry using HLA-DR and CD68 markers to assess microglial activation.
  • Measurement of MPO activity in MS cortical homogenates.

Main Results:

  • Significantly higher HLA-DR immunolabeling in demyelinated MS cortex compared to control cortex.
  • Increased microglial activation within MS cortical lesions versus non-demyelinated areas.
  • Elevated MPO activity in MS cortex associated with demyelination, with MPO localized to CD68-positive microglia within cortical plaques.

Conclusions:

  • Cortical demyelination in MS is associated with increased MPO activity.
  • Activated microglia expressing MPO are present in demyelinated cortical lesions.
  • Microglial production of ROS is implicated in the pathogenesis of cortical demyelination in MS.