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The activation of dormant ependymal cells following spinal cord injury

Ependymal cells, a dormant population of ciliated progenitors found within the central canal of the spinal cord, undergo significant alterations after spinal cord injury (SCI). Understanding the molecular events that induce ependymal cell activation after SCI represents the first step toward control...

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Autores principales: Rodriguez-Jimenez, Francisco Javier, Jendelova, Pavla, Erceg, Slaven
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10324230/
https://www.ncbi.nlm.nih.gov/pubmed/37408068
http://dx.doi.org/10.1186/s13287-023-03395-4
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author Rodriguez-Jimenez, Francisco Javier
Jendelova, Pavla
Erceg, Slaven
author_facet Rodriguez-Jimenez, Francisco Javier
Jendelova, Pavla
Erceg, Slaven
author_sort Rodriguez-Jimenez, Francisco Javier
collection PubMed
description Ependymal cells, a dormant population of ciliated progenitors found within the central canal of the spinal cord, undergo significant alterations after spinal cord injury (SCI). Understanding the molecular events that induce ependymal cell activation after SCI represents the first step toward controlling the response of the endogenous regenerative machinery in damaged tissues. This response involves the activation of specific signaling pathways in the spinal cord that promotes self-renewal, proliferation, and differentiation. We review our current understanding of the signaling pathways and molecular events that mediate the SCI-induced activation of ependymal cells by focusing on the roles of some cell adhesion molecules, cellular membrane receptors, ion channels (and their crosstalk), and transcription factors. An orchestrated response regulating the expression of receptors and ion channels fine-tunes and coordinates the activation of ependymal cells after SCI or cell transplantation. Understanding the major players in the activation of ependymal cells may help us to understand whether these cells represent a critical source of cells contributing to cellular replacement and tissue regeneration after SCI. A more complete understanding of the role and function of individual signaling pathways in endogenous spinal cord progenitors may foster the development of novel targeted therapies to induce the regeneration of the injured spinal cord.
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spelling pubmed-103242302023-07-07 The activation of dormant ependymal cells following spinal cord injury Rodriguez-Jimenez, Francisco Javier Jendelova, Pavla Erceg, Slaven Stem Cell Res Ther Review Ependymal cells, a dormant population of ciliated progenitors found within the central canal of the spinal cord, undergo significant alterations after spinal cord injury (SCI). Understanding the molecular events that induce ependymal cell activation after SCI represents the first step toward controlling the response of the endogenous regenerative machinery in damaged tissues. This response involves the activation of specific signaling pathways in the spinal cord that promotes self-renewal, proliferation, and differentiation. We review our current understanding of the signaling pathways and molecular events that mediate the SCI-induced activation of ependymal cells by focusing on the roles of some cell adhesion molecules, cellular membrane receptors, ion channels (and their crosstalk), and transcription factors. An orchestrated response regulating the expression of receptors and ion channels fine-tunes and coordinates the activation of ependymal cells after SCI or cell transplantation. Understanding the major players in the activation of ependymal cells may help us to understand whether these cells represent a critical source of cells contributing to cellular replacement and tissue regeneration after SCI. A more complete understanding of the role and function of individual signaling pathways in endogenous spinal cord progenitors may foster the development of novel targeted therapies to induce the regeneration of the injured spinal cord. BioMed Central 2023-07-05 /pmc/articles/PMC10324230/ /pubmed/37408068 http://dx.doi.org/10.1186/s13287-023-03395-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Review
Rodriguez-Jimenez, Francisco Javier
Jendelova, Pavla
Erceg, Slaven
The activation of dormant ependymal cells following spinal cord injury
title The activation of dormant ependymal cells following spinal cord injury
title_full The activation of dormant ependymal cells following spinal cord injury
title_fullStr The activation of dormant ependymal cells following spinal cord injury
title_full_unstemmed The activation of dormant ependymal cells following spinal cord injury
title_short The activation of dormant ependymal cells following spinal cord injury
title_sort activation of dormant ependymal cells following spinal cord injury
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10324230/
https://www.ncbi.nlm.nih.gov/pubmed/37408068
http://dx.doi.org/10.1186/s13287-023-03395-4
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