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Factors regulating microglia activation

Microglia are resident macrophages of the central nervous system (CNS) that display high functional similarities to other tissue macrophages. However, it is especially important to create and maintain an intact tissue homeostasis to support the neuronal cells, which are very sensitive even to minor...

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Detalles Bibliográficos
Autores principales: Kierdorf, Katrin, Prinz, Marco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3632747/
https://www.ncbi.nlm.nih.gov/pubmed/23630462
http://dx.doi.org/10.3389/fncel.2013.00044
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author Kierdorf, Katrin
Prinz, Marco
author_facet Kierdorf, Katrin
Prinz, Marco
author_sort Kierdorf, Katrin
collection PubMed
description Microglia are resident macrophages of the central nervous system (CNS) that display high functional similarities to other tissue macrophages. However, it is especially important to create and maintain an intact tissue homeostasis to support the neuronal cells, which are very sensitive even to minor changes in their environment. The transition from the “resting” but surveying microglial phenotype to an activated stage is tightly regulated by several intrinsic (e.g., Runx-1, Irf8, and Pu.1) and extrinsic factors (e.g., CD200, CX(3)CR1, and TREM2). Under physiological conditions, minor changes of those factors are sufficient to cause fatal dysregulation of microglial cell homeostasis and result in severe CNS pathologies. In this review, we discuss recent achievements that gave new insights into mechanisms that ensure microglia quiescence.
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spelling pubmed-36327472013-04-29 Factors regulating microglia activation Kierdorf, Katrin Prinz, Marco Front Cell Neurosci Neuroscience Microglia are resident macrophages of the central nervous system (CNS) that display high functional similarities to other tissue macrophages. However, it is especially important to create and maintain an intact tissue homeostasis to support the neuronal cells, which are very sensitive even to minor changes in their environment. The transition from the “resting” but surveying microglial phenotype to an activated stage is tightly regulated by several intrinsic (e.g., Runx-1, Irf8, and Pu.1) and extrinsic factors (e.g., CD200, CX(3)CR1, and TREM2). Under physiological conditions, minor changes of those factors are sufficient to cause fatal dysregulation of microglial cell homeostasis and result in severe CNS pathologies. In this review, we discuss recent achievements that gave new insights into mechanisms that ensure microglia quiescence. Frontiers Media S.A. 2013-04-23 /pmc/articles/PMC3632747/ /pubmed/23630462 http://dx.doi.org/10.3389/fncel.2013.00044 Text en Copyright © Kierdorf and Prinz. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.
spellingShingle Neuroscience
Kierdorf, Katrin
Prinz, Marco
Factors regulating microglia activation
title Factors regulating microglia activation
title_full Factors regulating microglia activation
title_fullStr Factors regulating microglia activation
title_full_unstemmed Factors regulating microglia activation
title_short Factors regulating microglia activation
title_sort factors regulating microglia activation
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3632747/
https://www.ncbi.nlm.nih.gov/pubmed/23630462
http://dx.doi.org/10.3389/fncel.2013.00044
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