4.3 Article

Neuromyelitis optica: a demyelinating disease characterized by acute destruction and regeneration of perivascular astrocytes

Journal

MULTIPLE SCLEROSIS JOURNAL
Volume 16, Issue 10, Pages 1156-1172

Publisher

SAGE PUBLICATIONS LTD
DOI: 10.1177/1352458510382324

Keywords

apoptosis; Devic's disease; glial progenitors; myelin

Funding

  1. Multiple Sclerosis Research Australia
  2. Neil and Norma Hill Research Fellowship
  3. Nerve Research Foundation, University of Sydney
  4. NSW Ministry For Science And Medical Research
  5. Ramaciotti foundation
  6. Biogen Idec post-graduate scholarship

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Objective: To determine whether there is an astrocyte lesion in NMO and if this differs from astrocyte changes in multiple sclerosis (MS). Methods: Astrocyte pathology in early (still-myelinated) lesions and subacute NMO and MS lesions was examined immunohistochemically and in sections stained for astrocytes using routine histological techniques. Results: Demyelination in early NMO lesions is accompanied by oligodendrocyte apoptosis in a pattern identical to that seen in MS and this is preceded by an abrupt destruction of perivascular astrocytes. Reparative astrogliosis is effected by a population of unipolar, new astrocytes. Evidence of a different type of astrocyte lesion was found in MS. Discussion: The findings add to experimental evidence that the antibody is pathogenic. They also raise the possibility that demyelination in MS may be a bystander effect of an astrocyte lesion, i.e. that MS is not a disease primarily of myelin and oligodendrocytes.

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