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The origin of remyelinating oligodendrocytes in antiserum-mediated demtelinative optic neuropathy
Journal article   Peer reviewed

The origin of remyelinating oligodendrocytes in antiserum-mediated demtelinative optic neuropathy

W.M. Carroll, A.R. Jennings and F.L. Mastaglia
Brain, Vol.113(4), pp.953-973
1990
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Abstract

The origin of the remyelinating oligodendrocyte in a focal antigalactocerebroside-induced demyelinating lesion of the cat optic nerve was studied with detailed correlative electron microscopy and immunocytochemistry using a panel of antigenic makers. Within 10 days of the destruction of all endogenous oligodendrocytes and demyelination of all axons in the lesion, a new population of small glial cells appeared coincident with division of the residual astrocytes and developed a process-bearing axon-embracing morphology. The processes of these small glial cells (SGCs) contained intermediate filaments composed not of glial fibrillary acidic protein but of vimentin and over the ensuing 14 days these cells confirmed their oligodendrocyte destiny by differentiating to lose the intermediate filaments, form myelin and acquire the typical oligodendrocyte antigenic phenotype. It is suggested that the extensive remyelination of this lesion is sponsored by the new population of SGCs which in turn are generated either by differentiated reactive astrocytes or by as yet unidentified precursor cells.

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Collaboration types
Domestic collaboration
Citation topics
1 Clinical & Life Sciences
1.203 Neuromuscular Disorders
1.203.1430 Oligodendrocyte Myelination
Web Of Science research areas
Clinical Neurology
Neurosciences
ESI research areas
Neuroscience & Behavior
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