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The role of neural stem cells in regulating glial scar formation and repair
Glial scars are a common pathological occurrence in a variety of central nervous system (CNS) diseases and injuries. They are caused after severe damage and consist of reactive glia that form a barrier around the damaged tissue that leads to a non-permissive microenvironment which prevents proper en...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8975756/ https://www.ncbi.nlm.nih.gov/pubmed/34820704 http://dx.doi.org/10.1007/s00441-021-03554-0 |
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author | Nicaise, Alexandra M. D’Angelo, Andrea Ionescu, Rosana-Bristena Krzak, Grzegorz Willis, Cory M. Pluchino, Stefano |
author_facet | Nicaise, Alexandra M. D’Angelo, Andrea Ionescu, Rosana-Bristena Krzak, Grzegorz Willis, Cory M. Pluchino, Stefano |
author_sort | Nicaise, Alexandra M. |
collection | PubMed |
description | Glial scars are a common pathological occurrence in a variety of central nervous system (CNS) diseases and injuries. They are caused after severe damage and consist of reactive glia that form a barrier around the damaged tissue that leads to a non-permissive microenvironment which prevents proper endogenous regeneration. While there are a number of therapies that are able to address some components of disease, there are none that provide regenerative properties. Within the past decade, neural stem cells (NSCs) have been heavily studied due to their potent anti-inflammatory and reparative capabilities in disease and injury. Exogenously applied NSCs have been found to aid in glial scar healing by reducing inflammation and providing cell replacement. However, endogenous NSCs have also been found to contribute to the reactive environment by different means. Further understanding how NSCs can be leveraged to aid in the resolution of the glial scar is imperative in the use of these cells as regenerative therapies. To do so, humanised 3D model systems have been developed to study the development and maintenance of the glial scar. Herein, we explore the current work on endogenous and exogenous NSCs in the glial scar as well as the novel 3D stem cell–based technologies being used to model this pathology in a dish. |
format | Online Article Text |
id | pubmed-8975756 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-89757562022-04-07 The role of neural stem cells in regulating glial scar formation and repair Nicaise, Alexandra M. D’Angelo, Andrea Ionescu, Rosana-Bristena Krzak, Grzegorz Willis, Cory M. Pluchino, Stefano Cell Tissue Res Review Glial scars are a common pathological occurrence in a variety of central nervous system (CNS) diseases and injuries. They are caused after severe damage and consist of reactive glia that form a barrier around the damaged tissue that leads to a non-permissive microenvironment which prevents proper endogenous regeneration. While there are a number of therapies that are able to address some components of disease, there are none that provide regenerative properties. Within the past decade, neural stem cells (NSCs) have been heavily studied due to their potent anti-inflammatory and reparative capabilities in disease and injury. Exogenously applied NSCs have been found to aid in glial scar healing by reducing inflammation and providing cell replacement. However, endogenous NSCs have also been found to contribute to the reactive environment by different means. Further understanding how NSCs can be leveraged to aid in the resolution of the glial scar is imperative in the use of these cells as regenerative therapies. To do so, humanised 3D model systems have been developed to study the development and maintenance of the glial scar. Herein, we explore the current work on endogenous and exogenous NSCs in the glial scar as well as the novel 3D stem cell–based technologies being used to model this pathology in a dish. Springer Berlin Heidelberg 2021-11-25 2022 /pmc/articles/PMC8975756/ /pubmed/34820704 http://dx.doi.org/10.1007/s00441-021-03554-0 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Review Nicaise, Alexandra M. D’Angelo, Andrea Ionescu, Rosana-Bristena Krzak, Grzegorz Willis, Cory M. Pluchino, Stefano The role of neural stem cells in regulating glial scar formation and repair |
title | The role of neural stem cells in regulating glial scar formation and repair |
title_full | The role of neural stem cells in regulating glial scar formation and repair |
title_fullStr | The role of neural stem cells in regulating glial scar formation and repair |
title_full_unstemmed | The role of neural stem cells in regulating glial scar formation and repair |
title_short | The role of neural stem cells in regulating glial scar formation and repair |
title_sort | role of neural stem cells in regulating glial scar formation and repair |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8975756/ https://www.ncbi.nlm.nih.gov/pubmed/34820704 http://dx.doi.org/10.1007/s00441-021-03554-0 |
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