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Targeting the Subventricular Zone to Promote Myelin Repair in the Aging Brain
The subventricular zone (SVZ) is the largest and most active germinal zone in the adult forebrain. Neural stem cells (NSCs) of the SVZ generate olfactory interneurons throughout life and retain the intrinsic ability to generate oligodendrocytes (OLs), the myelinating cells of the central nervous sys...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9180001/ https://www.ncbi.nlm.nih.gov/pubmed/35681504 http://dx.doi.org/10.3390/cells11111809 |
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author | Butt, Arthur Morgan Rivera, Andrea Dominico Fulton, Daniel Azim, Kasum |
author_facet | Butt, Arthur Morgan Rivera, Andrea Dominico Fulton, Daniel Azim, Kasum |
author_sort | Butt, Arthur Morgan |
collection | PubMed |
description | The subventricular zone (SVZ) is the largest and most active germinal zone in the adult forebrain. Neural stem cells (NSCs) of the SVZ generate olfactory interneurons throughout life and retain the intrinsic ability to generate oligodendrocytes (OLs), the myelinating cells of the central nervous system. OLs and myelin are targets in demyelinating diseases such as multiple sclerosis (MS). Remyelination is dependent on the ability of oligodendrocyte progenitor cells (OPCs) to proliferate, migrate, and terminally differentiate into myelinating OLs. During aging, there is a gradual decrease in the regenerative capacity of OPCs, and the consequent loss of OLs and myelin is a contributing factor in cognitive decline and the failure of remyelination in MS and other pathologies with aging contexts, including Alzheimer’s disease (AD) and stroke. The age-related decrease in oligodendrogenesis has not been fully characterised but is known to reflect changes in intrinsic and environmental factors affecting the ability of OPCs to respond to pro-differentiation stimuli. Notably, SVZ-derived OPCs are an important source of remyelinating OLs in addition to parenchymal OPCs. In this mini-review, we briefly discuss differences between SVZ-derived and parenchymal OPCs in their responses to demyelination and highlight challenges associated with their study in vivo and how they can be targeted for regenerative therapies in the aged brain. |
format | Online Article Text |
id | pubmed-9180001 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-91800012022-06-10 Targeting the Subventricular Zone to Promote Myelin Repair in the Aging Brain Butt, Arthur Morgan Rivera, Andrea Dominico Fulton, Daniel Azim, Kasum Cells Review The subventricular zone (SVZ) is the largest and most active germinal zone in the adult forebrain. Neural stem cells (NSCs) of the SVZ generate olfactory interneurons throughout life and retain the intrinsic ability to generate oligodendrocytes (OLs), the myelinating cells of the central nervous system. OLs and myelin are targets in demyelinating diseases such as multiple sclerosis (MS). Remyelination is dependent on the ability of oligodendrocyte progenitor cells (OPCs) to proliferate, migrate, and terminally differentiate into myelinating OLs. During aging, there is a gradual decrease in the regenerative capacity of OPCs, and the consequent loss of OLs and myelin is a contributing factor in cognitive decline and the failure of remyelination in MS and other pathologies with aging contexts, including Alzheimer’s disease (AD) and stroke. The age-related decrease in oligodendrogenesis has not been fully characterised but is known to reflect changes in intrinsic and environmental factors affecting the ability of OPCs to respond to pro-differentiation stimuli. Notably, SVZ-derived OPCs are an important source of remyelinating OLs in addition to parenchymal OPCs. In this mini-review, we briefly discuss differences between SVZ-derived and parenchymal OPCs in their responses to demyelination and highlight challenges associated with their study in vivo and how they can be targeted for regenerative therapies in the aged brain. MDPI 2022-05-31 /pmc/articles/PMC9180001/ /pubmed/35681504 http://dx.doi.org/10.3390/cells11111809 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Butt, Arthur Morgan Rivera, Andrea Dominico Fulton, Daniel Azim, Kasum Targeting the Subventricular Zone to Promote Myelin Repair in the Aging Brain |
title | Targeting the Subventricular Zone to Promote Myelin Repair in the Aging Brain |
title_full | Targeting the Subventricular Zone to Promote Myelin Repair in the Aging Brain |
title_fullStr | Targeting the Subventricular Zone to Promote Myelin Repair in the Aging Brain |
title_full_unstemmed | Targeting the Subventricular Zone to Promote Myelin Repair in the Aging Brain |
title_short | Targeting the Subventricular Zone to Promote Myelin Repair in the Aging Brain |
title_sort | targeting the subventricular zone to promote myelin repair in the aging brain |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9180001/ https://www.ncbi.nlm.nih.gov/pubmed/35681504 http://dx.doi.org/10.3390/cells11111809 |
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