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Oligodendrocyte Lineage Cells in Chronic Demyelination of Multiple Sclerosis Optic Nerve
Reports that chronically demyelinated multiple sclerosis brain and spinal cord lesions contained immature oligodendrocyte lineage cells have generated major interest aimed at the potential for promotion of endogenous repair. Despite the prominence of the optic nerve as a lesion site and its importan...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8028859/ https://www.ncbi.nlm.nih.gov/pubmed/25175564 http://dx.doi.org/10.1111/bpa.12193 |
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author | Jennings, Alison Ruth Carroll, William M. |
author_facet | Jennings, Alison Ruth Carroll, William M. |
author_sort | Jennings, Alison Ruth |
collection | PubMed |
description | Reports that chronically demyelinated multiple sclerosis brain and spinal cord lesions contained immature oligodendrocyte lineage cells have generated major interest aimed at the potential for promotion of endogenous repair. Despite the prominence of the optic nerve as a lesion site and its importance in clinical disease assessment, no detailed studies of multiple sclerosis‐affected optic nerve exist. This study aims to provide insight into the cellular pathology of chronic demyelination in multiple sclerosis through direct morphological and immunohistochemical analysis of optic nerve in conjunction with observations from an experimental cat optic nerve model of successful remyelination. Myelin staining was followed by immunohistochemistry to differentially label neuroglia. Digitally immortalized sections were then analyzed to generate quantification data and antigenic phenotypes including maturational stages within the oligodendrocyte lineage. It was found that some chronically demyelinated multiple sclerosis optic nerve lesions contained oligodendroglial cells and that heterogeneity existed in the presence of myelin sheaths, oligodendrocyte maturational stages and extent of axonal investment. The findings advance our understanding of oligodendrocyte activity in chronically demyelinated human optic nerve and may have implications for studies aimed at enhancement of endogenous repair in multiple sclerosis. |
format | Online Article Text |
id | pubmed-8028859 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-80288592021-09-03 Oligodendrocyte Lineage Cells in Chronic Demyelination of Multiple Sclerosis Optic Nerve Jennings, Alison Ruth Carroll, William M. Brain Pathol Research Articles Reports that chronically demyelinated multiple sclerosis brain and spinal cord lesions contained immature oligodendrocyte lineage cells have generated major interest aimed at the potential for promotion of endogenous repair. Despite the prominence of the optic nerve as a lesion site and its importance in clinical disease assessment, no detailed studies of multiple sclerosis‐affected optic nerve exist. This study aims to provide insight into the cellular pathology of chronic demyelination in multiple sclerosis through direct morphological and immunohistochemical analysis of optic nerve in conjunction with observations from an experimental cat optic nerve model of successful remyelination. Myelin staining was followed by immunohistochemistry to differentially label neuroglia. Digitally immortalized sections were then analyzed to generate quantification data and antigenic phenotypes including maturational stages within the oligodendrocyte lineage. It was found that some chronically demyelinated multiple sclerosis optic nerve lesions contained oligodendroglial cells and that heterogeneity existed in the presence of myelin sheaths, oligodendrocyte maturational stages and extent of axonal investment. The findings advance our understanding of oligodendrocyte activity in chronically demyelinated human optic nerve and may have implications for studies aimed at enhancement of endogenous repair in multiple sclerosis. John Wiley and Sons Inc. 2014-10-29 /pmc/articles/PMC8028859/ /pubmed/25175564 http://dx.doi.org/10.1111/bpa.12193 Text en © 2014 The Authors. Brain Pathology published by John Wiley & Sons Ltd on behalf of International Society of Neuropathology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Research Articles Jennings, Alison Ruth Carroll, William M. Oligodendrocyte Lineage Cells in Chronic Demyelination of Multiple Sclerosis Optic Nerve |
title | Oligodendrocyte Lineage Cells in Chronic Demyelination of Multiple Sclerosis Optic Nerve |
title_full | Oligodendrocyte Lineage Cells in Chronic Demyelination of Multiple Sclerosis Optic Nerve |
title_fullStr | Oligodendrocyte Lineage Cells in Chronic Demyelination of Multiple Sclerosis Optic Nerve |
title_full_unstemmed | Oligodendrocyte Lineage Cells in Chronic Demyelination of Multiple Sclerosis Optic Nerve |
title_short | Oligodendrocyte Lineage Cells in Chronic Demyelination of Multiple Sclerosis Optic Nerve |
title_sort | oligodendrocyte lineage cells in chronic demyelination of multiple sclerosis optic nerve |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8028859/ https://www.ncbi.nlm.nih.gov/pubmed/25175564 http://dx.doi.org/10.1111/bpa.12193 |
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