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The Role of Astrocytes in Neuroprotection after Brain Stroke: Potential in Cell Therapy

Astrocytes are commonly involved in negative responses through their hyperreactivity and glial scar formation in excitotoxic and/or mechanical injuries. But, astrocytes are also specialized glial cells of the nervous system that perform multiple homeostatic functions for the survival and maintenance...

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Autores principales: Becerra-Calixto, Andrea, Cardona-Gómez, Gloria P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5376556/
https://www.ncbi.nlm.nih.gov/pubmed/28420961
http://dx.doi.org/10.3389/fnmol.2017.00088
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author Becerra-Calixto, Andrea
Cardona-Gómez, Gloria P.
author_facet Becerra-Calixto, Andrea
Cardona-Gómez, Gloria P.
author_sort Becerra-Calixto, Andrea
collection PubMed
description Astrocytes are commonly involved in negative responses through their hyperreactivity and glial scar formation in excitotoxic and/or mechanical injuries. But, astrocytes are also specialized glial cells of the nervous system that perform multiple homeostatic functions for the survival and maintenance of the neurovascular unit. Astrocytes have neuroprotective, angiogenic, immunomodulatory, neurogenic, and antioxidant properties and modulate synaptic function. This makes them excellent candidates as a source of neuroprotection and neurorestoration in tissues affected by ischemia/reperfusion, when some of their deregulated genes can be controlled. Therefore, this review analyzes pro-survival responses of astrocytes that would allow their use in cell therapy strategies.
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spelling pubmed-53765562017-04-18 The Role of Astrocytes in Neuroprotection after Brain Stroke: Potential in Cell Therapy Becerra-Calixto, Andrea Cardona-Gómez, Gloria P. Front Mol Neurosci Neuroscience Astrocytes are commonly involved in negative responses through their hyperreactivity and glial scar formation in excitotoxic and/or mechanical injuries. But, astrocytes are also specialized glial cells of the nervous system that perform multiple homeostatic functions for the survival and maintenance of the neurovascular unit. Astrocytes have neuroprotective, angiogenic, immunomodulatory, neurogenic, and antioxidant properties and modulate synaptic function. This makes them excellent candidates as a source of neuroprotection and neurorestoration in tissues affected by ischemia/reperfusion, when some of their deregulated genes can be controlled. Therefore, this review analyzes pro-survival responses of astrocytes that would allow their use in cell therapy strategies. Frontiers Media S.A. 2017-04-03 /pmc/articles/PMC5376556/ /pubmed/28420961 http://dx.doi.org/10.3389/fnmol.2017.00088 Text en Copyright © 2017 Becerra-Calixto and Cardona-Gómez. http://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) or licensor 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 Neuroscience
Becerra-Calixto, Andrea
Cardona-Gómez, Gloria P.
The Role of Astrocytes in Neuroprotection after Brain Stroke: Potential in Cell Therapy
title The Role of Astrocytes in Neuroprotection after Brain Stroke: Potential in Cell Therapy
title_full The Role of Astrocytes in Neuroprotection after Brain Stroke: Potential in Cell Therapy
title_fullStr The Role of Astrocytes in Neuroprotection after Brain Stroke: Potential in Cell Therapy
title_full_unstemmed The Role of Astrocytes in Neuroprotection after Brain Stroke: Potential in Cell Therapy
title_short The Role of Astrocytes in Neuroprotection after Brain Stroke: Potential in Cell Therapy
title_sort role of astrocytes in neuroprotection after brain stroke: potential in cell therapy
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5376556/
https://www.ncbi.nlm.nih.gov/pubmed/28420961
http://dx.doi.org/10.3389/fnmol.2017.00088
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