Cargando…
Tenascins Interfere With Remyelination in an Ex Vivo Cerebellar Explant Model of Demyelination
Oligodendrocytes form myelin membranes and thereby secure the insulation of axons and the rapid conduction of action potentials. Diseases such as multiple sclerosis highlight the importance of this glial cell population for brain function. In the adult brain, efficient remyelination following the da...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8965512/ https://www.ncbi.nlm.nih.gov/pubmed/35372366 http://dx.doi.org/10.3389/fcell.2022.819967 |
_version_ | 1784678450611617792 |
---|---|
author | Bauch, Juliane Ort, Sina Vom Ulc, Annika Faissner, Andreas |
author_facet | Bauch, Juliane Ort, Sina Vom Ulc, Annika Faissner, Andreas |
author_sort | Bauch, Juliane |
collection | PubMed |
description | Oligodendrocytes form myelin membranes and thereby secure the insulation of axons and the rapid conduction of action potentials. Diseases such as multiple sclerosis highlight the importance of this glial cell population for brain function. In the adult brain, efficient remyelination following the damage to oligodendrocytes is compromised. Myelination is characterized by proliferation, migration, and proper integration of oligodendrocyte precursor cells (OPCs). These processes are among others controlled by proteins of the extracellular matrix (ECM). As a prominent representative ECM molecule, tenascin-C (Tnc) exerts an inhibitory effect on the migration and differentiation of OPCs. The structurally similar paralogue tenascin-R (Tnr) is known to promote the differentiation of oligodendrocytes. The model of lysolecithin-induced demyelination of cerebellar slice cultures represents an important tool for the analysis of the remyelination process. Ex vivo cerebellar explant cultures of Tnc ( −/− ) and Tnr ( −/− ) mouse lines displayed enhanced remyelination by forming thicker myelin membranes upon exposure to lysolecithin. The inhibitory effect of tenascins on remyelination could be confirmed when demyelinated wildtype control cultures were exposed to purified Tnc or Tnr protein. In that approach, the remyelination efficiency decreased in a dose-dependent manner with increasing concentrations of ECM molecules added. In order to examine potential roles in a complex in vivo environment, we successfully established cuprizone-based acute demyelination to analyze the remyelination behavior after cuprizone withdrawal in SV129, Tnc ( −/− ), and Tnr ( −/− ) mice. In addition, we documented by immunohistochemistry in the cuprizone model the expression of chondroitin sulfate proteoglycans that are inhibitory for the differentiation of OPCs. In conclusion, inhibitory properties of Tnc and Tnr for myelin membrane formation could be demonstrated by using an ex vivo approach. |
format | Online Article Text |
id | pubmed-8965512 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-89655122022-03-31 Tenascins Interfere With Remyelination in an Ex Vivo Cerebellar Explant Model of Demyelination Bauch, Juliane Ort, Sina Vom Ulc, Annika Faissner, Andreas Front Cell Dev Biol Cell and Developmental Biology Oligodendrocytes form myelin membranes and thereby secure the insulation of axons and the rapid conduction of action potentials. Diseases such as multiple sclerosis highlight the importance of this glial cell population for brain function. In the adult brain, efficient remyelination following the damage to oligodendrocytes is compromised. Myelination is characterized by proliferation, migration, and proper integration of oligodendrocyte precursor cells (OPCs). These processes are among others controlled by proteins of the extracellular matrix (ECM). As a prominent representative ECM molecule, tenascin-C (Tnc) exerts an inhibitory effect on the migration and differentiation of OPCs. The structurally similar paralogue tenascin-R (Tnr) is known to promote the differentiation of oligodendrocytes. The model of lysolecithin-induced demyelination of cerebellar slice cultures represents an important tool for the analysis of the remyelination process. Ex vivo cerebellar explant cultures of Tnc ( −/− ) and Tnr ( −/− ) mouse lines displayed enhanced remyelination by forming thicker myelin membranes upon exposure to lysolecithin. The inhibitory effect of tenascins on remyelination could be confirmed when demyelinated wildtype control cultures were exposed to purified Tnc or Tnr protein. In that approach, the remyelination efficiency decreased in a dose-dependent manner with increasing concentrations of ECM molecules added. In order to examine potential roles in a complex in vivo environment, we successfully established cuprizone-based acute demyelination to analyze the remyelination behavior after cuprizone withdrawal in SV129, Tnc ( −/− ), and Tnr ( −/− ) mice. In addition, we documented by immunohistochemistry in the cuprizone model the expression of chondroitin sulfate proteoglycans that are inhibitory for the differentiation of OPCs. In conclusion, inhibitory properties of Tnc and Tnr for myelin membrane formation could be demonstrated by using an ex vivo approach. Frontiers Media S.A. 2022-03-15 /pmc/articles/PMC8965512/ /pubmed/35372366 http://dx.doi.org/10.3389/fcell.2022.819967 Text en Copyright © 2022 Bauch, Ort, Ulc and Faissner. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cell and Developmental Biology Bauch, Juliane Ort, Sina Vom Ulc, Annika Faissner, Andreas Tenascins Interfere With Remyelination in an Ex Vivo Cerebellar Explant Model of Demyelination |
title | Tenascins Interfere With Remyelination in an Ex Vivo Cerebellar Explant Model of Demyelination |
title_full | Tenascins Interfere With Remyelination in an Ex Vivo Cerebellar Explant Model of Demyelination |
title_fullStr | Tenascins Interfere With Remyelination in an Ex Vivo Cerebellar Explant Model of Demyelination |
title_full_unstemmed | Tenascins Interfere With Remyelination in an Ex Vivo Cerebellar Explant Model of Demyelination |
title_short | Tenascins Interfere With Remyelination in an Ex Vivo Cerebellar Explant Model of Demyelination |
title_sort | tenascins interfere with remyelination in an ex vivo cerebellar explant model of demyelination |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8965512/ https://www.ncbi.nlm.nih.gov/pubmed/35372366 http://dx.doi.org/10.3389/fcell.2022.819967 |
work_keys_str_mv | AT bauchjuliane tenascinsinterferewithremyelinationinanexvivocerebellarexplantmodelofdemyelination AT ortsinavom tenascinsinterferewithremyelinationinanexvivocerebellarexplantmodelofdemyelination AT ulcannika tenascinsinterferewithremyelinationinanexvivocerebellarexplantmodelofdemyelination AT faissnerandreas tenascinsinterferewithremyelinationinanexvivocerebellarexplantmodelofdemyelination |