4.3 Article

Multiple Sclerosis: Destruction and Regeneration of Astrocytes in Acute Lesions

期刊

出版社

OXFORD UNIV PRESS INC
DOI: 10.1093/jnen/nly121

关键词

Astrocytes; Aquaporin4; Blood-brain barrier; Conduction block; KIR4; 1; Neuromyelitis optica; Secondary progressive MS

资金

  1. Multiple Sclerosis Research Australia
  2. Nerve Research Foundation University of Sydney
  3. National Multiple Sclerosis Society [JWP RG 2731-A-B]
  4. NSW Ministry for Science and Medical Research
  5. University of Sydney
  6. National Health and Medical Research Council of Australia
  7. National Neurological Research Specimen Bank, VAMC Wadsworth Division, Los Angeles, California - NINDS/NIMH
  8. National Multiple Sclerosis Society
  9. Hereditary Disease Research Foundation
  10. Comprehensive Epilepsy Program
  11. Tourette Syndrome Association
  12. Dystonia Medical Research Foundation
  13. Veterans Health Services and Research Administration, Department of Veterans Affairs

向作者/读者索取更多资源

There are reports that astrocyte perivascular endfeet are damaged in some cases of multiple sclerosis (MS). This study was designed to determine the origin and outcome of astrocyte damage in acute, resolving, and inactive plaques. Ten acute plaques from 10 early MS cases and 14 plaques of differing histological age from 9 subacute and chronic cases were examined immunohistochemically. Also examined were nonnecrotic early lesions in 3 patients with neuromyelitis optica (NMO). Plaques from 3 MS cases were examined electron microscopically. The edge zones in each of the 10 acute MS lesions revealed a complete loss of astrocyte cell bodies and their pericapillary, perineuronal, and perivascular foot processes. Dendrophagocytosis of degenerate astrocytes was observed. Astrocyte precursors, similar to those that replace destroyed astrocytes in nonnecrotic NMO lesions, were present in areas depleted of astrocytes. Resolving plaques were repopulated initially by stellate astrocytes that stained negatively for the water channel molecule aquaporin4 (AQP4). In older lesions, astrocytes were predominantly AQP4-positive. Loss and recovery of astrocytes in new MS lesions may be as important as myelin loss as a cause of conduction block responsible for symptoms in patients with relapsing and remitting and secondary progressive MS.

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