A morphological analysis of activity-dependent myelination and myelin injury in transitional oligodendrocytes

Abstract Neuronal activity is established as a driver of oligodendrocyte (OL) differentiation and myelination. The concept of activity-dependent myelin plasticity, and its role in cognition and disease, is gaining support. Methods capable of resolving changes in the morphology of individual myelinat...

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Main Authors: Eszter Toth, Sayed Muhammed Rassul, Martin Berry, Daniel Fulton
Format: Article
Language:English
Published: Nature Publishing Group 2021-05-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-021-88887-0
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spelling doaj-ee8adcc82dcb4e94a938ef11d7709eb12021-05-09T11:32:26ZengNature Publishing GroupScientific Reports2045-23222021-05-0111111410.1038/s41598-021-88887-0A morphological analysis of activity-dependent myelination and myelin injury in transitional oligodendrocytesEszter Toth0Sayed Muhammed Rassul1Martin Berry2Daniel Fulton3Neuroscience and Ophthalmology Research Group, Institute of Inflammation and Ageing, College of Medical and Dental Sciences, University of BirminghamNeuroscience and Ophthalmology Research Group, Institute of Inflammation and Ageing, College of Medical and Dental Sciences, University of BirminghamNeuroscience and Ophthalmology Research Group, Institute of Inflammation and Ageing, College of Medical and Dental Sciences, University of BirminghamNeuroscience and Ophthalmology Research Group, Institute of Inflammation and Ageing, College of Medical and Dental Sciences, University of BirminghamAbstract Neuronal activity is established as a driver of oligodendrocyte (OL) differentiation and myelination. The concept of activity-dependent myelin plasticity, and its role in cognition and disease, is gaining support. Methods capable of resolving changes in the morphology of individual myelinating OL would advance our understanding of myelin plasticity and injury, thus we adapted a labelling approach involving Semliki Forest Virus (SFV) vectors to resolve and quantify the 3-D structure of OL processes and internodes in cerebellar slice cultures. We first demonstrate the utility of the approach by studying changes in OL morphology after complement-mediated injury. SFV vectors injected into cerebellar white matter labelled transitional OL (TOL), whose characteristic mixture of myelinating and non-myelinating processes exhibited significant degeneration after complement injury. The method was also capable of resolving finer changes in morphology related to neuronal activity. Prolonged suppression of neuronal activity, which reduced myelination, selectively decreased the length of putative internodes, and the proportion of process branches that supported them, while leaving other features of process morphology unaltered. Overall this work provides novel information on the morphology of TOL, and their response to conditions that alter circuit function or induce demyelination.https://doi.org/10.1038/s41598-021-88887-0
collection DOAJ
language English
format Article
sources DOAJ
author Eszter Toth
Sayed Muhammed Rassul
Martin Berry
Daniel Fulton
spellingShingle Eszter Toth
Sayed Muhammed Rassul
Martin Berry
Daniel Fulton
A morphological analysis of activity-dependent myelination and myelin injury in transitional oligodendrocytes
Scientific Reports
author_facet Eszter Toth
Sayed Muhammed Rassul
Martin Berry
Daniel Fulton
author_sort Eszter Toth
title A morphological analysis of activity-dependent myelination and myelin injury in transitional oligodendrocytes
title_short A morphological analysis of activity-dependent myelination and myelin injury in transitional oligodendrocytes
title_full A morphological analysis of activity-dependent myelination and myelin injury in transitional oligodendrocytes
title_fullStr A morphological analysis of activity-dependent myelination and myelin injury in transitional oligodendrocytes
title_full_unstemmed A morphological analysis of activity-dependent myelination and myelin injury in transitional oligodendrocytes
title_sort morphological analysis of activity-dependent myelination and myelin injury in transitional oligodendrocytes
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2021-05-01
description Abstract Neuronal activity is established as a driver of oligodendrocyte (OL) differentiation and myelination. The concept of activity-dependent myelin plasticity, and its role in cognition and disease, is gaining support. Methods capable of resolving changes in the morphology of individual myelinating OL would advance our understanding of myelin plasticity and injury, thus we adapted a labelling approach involving Semliki Forest Virus (SFV) vectors to resolve and quantify the 3-D structure of OL processes and internodes in cerebellar slice cultures. We first demonstrate the utility of the approach by studying changes in OL morphology after complement-mediated injury. SFV vectors injected into cerebellar white matter labelled transitional OL (TOL), whose characteristic mixture of myelinating and non-myelinating processes exhibited significant degeneration after complement injury. The method was also capable of resolving finer changes in morphology related to neuronal activity. Prolonged suppression of neuronal activity, which reduced myelination, selectively decreased the length of putative internodes, and the proportion of process branches that supported them, while leaving other features of process morphology unaltered. Overall this work provides novel information on the morphology of TOL, and their response to conditions that alter circuit function or induce demyelination.
url https://doi.org/10.1038/s41598-021-88887-0
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