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Modulating Microglial Cells for Promoting Brain Recovery and Repair

Representing the brain’s innate immune cells that interact vividly with blood-derived immune cells and brain parenchymal cells, microglia set the stage for successful brain remodeling and repair in the aftermath of brain damage. With the development of pharmacological colony-stimulating factor-1 rec...

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Detalles Bibliográficos
Autores principales: Hermann, Dirk M., Gunzer, Matthias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7829249/
https://www.ncbi.nlm.nih.gov/pubmed/33505251
http://dx.doi.org/10.3389/fncel.2020.627987
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author Hermann, Dirk M.
Gunzer, Matthias
author_facet Hermann, Dirk M.
Gunzer, Matthias
author_sort Hermann, Dirk M.
collection PubMed
description Representing the brain’s innate immune cells that interact vividly with blood-derived immune cells and brain parenchymal cells, microglia set the stage for successful brain remodeling and repair in the aftermath of brain damage. With the development of pharmacological colony-stimulating factor-1 receptor inhibitors, which allow inhibiting or depleting microglial cells, and of transgenic mice, allowing the inducible depletion of microglial cells, experimental tools have become available for studying roles of microglia in neurodegenerative and neurorestorative processes. These models open fundamental insights into roles of microglia in controlling synaptic plasticity in the healthy and the injured brain. Acting as a switch from injury to repair, microglial cells might open opportunities for promoting neurological recovery in human patients upon brain injury.
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spelling pubmed-78292492021-01-26 Modulating Microglial Cells for Promoting Brain Recovery and Repair Hermann, Dirk M. Gunzer, Matthias Front Cell Neurosci Cellular Neuroscience Representing the brain’s innate immune cells that interact vividly with blood-derived immune cells and brain parenchymal cells, microglia set the stage for successful brain remodeling and repair in the aftermath of brain damage. With the development of pharmacological colony-stimulating factor-1 receptor inhibitors, which allow inhibiting or depleting microglial cells, and of transgenic mice, allowing the inducible depletion of microglial cells, experimental tools have become available for studying roles of microglia in neurodegenerative and neurorestorative processes. These models open fundamental insights into roles of microglia in controlling synaptic plasticity in the healthy and the injured brain. Acting as a switch from injury to repair, microglial cells might open opportunities for promoting neurological recovery in human patients upon brain injury. Frontiers Media S.A. 2021-01-11 /pmc/articles/PMC7829249/ /pubmed/33505251 http://dx.doi.org/10.3389/fncel.2020.627987 Text en Copyright © 2021 Hermann and Gunzer. 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) and the copyright owner(s) 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 Cellular Neuroscience
Hermann, Dirk M.
Gunzer, Matthias
Modulating Microglial Cells for Promoting Brain Recovery and Repair
title Modulating Microglial Cells for Promoting Brain Recovery and Repair
title_full Modulating Microglial Cells for Promoting Brain Recovery and Repair
title_fullStr Modulating Microglial Cells for Promoting Brain Recovery and Repair
title_full_unstemmed Modulating Microglial Cells for Promoting Brain Recovery and Repair
title_short Modulating Microglial Cells for Promoting Brain Recovery and Repair
title_sort modulating microglial cells for promoting brain recovery and repair
topic Cellular Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7829249/
https://www.ncbi.nlm.nih.gov/pubmed/33505251
http://dx.doi.org/10.3389/fncel.2020.627987
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