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Primary Phagocytosis of Neurons by Inflamed Microglia: Potential Roles in Neurodegeneration
Microglial phagocytosis of dead or dying neurons can be beneficial by preventing the release of damaging and/or pro-inflammatory intracellular components. However, there is now evidence that under certain conditions, such as inflammation, microglia can also phagocytose viable neurons, thus executing...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Research Foundation
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3288722/ https://www.ncbi.nlm.nih.gov/pubmed/22403545 http://dx.doi.org/10.3389/fphar.2012.00027 |
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author | Neher, Jonas J. Neniskyte, Urte Brown, Guy C. |
author_facet | Neher, Jonas J. Neniskyte, Urte Brown, Guy C. |
author_sort | Neher, Jonas J. |
collection | PubMed |
description | Microglial phagocytosis of dead or dying neurons can be beneficial by preventing the release of damaging and/or pro-inflammatory intracellular components. However, there is now evidence that under certain conditions, such as inflammation, microglia can also phagocytose viable neurons, thus executing their death. Such phagocytic cell death may result from exposure of phosphatidylserine (PS) or other eat-me signals on otherwise viable neurons as a result of physiological activation or sub-toxic insult, and neuronal phagocytosis by activated microglia. In this review, we discuss the mechanisms of phagocytic cell death and its potential roles in Alzheimer’s Disease, Parkinson’s Disease, and Frontotemporal Dementia. |
format | Online Article Text |
id | pubmed-3288722 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Frontiers Research Foundation |
record_format | MEDLINE/PubMed |
spelling | pubmed-32887222012-03-08 Primary Phagocytosis of Neurons by Inflamed Microglia: Potential Roles in Neurodegeneration Neher, Jonas J. Neniskyte, Urte Brown, Guy C. Front Pharmacol Pharmacology Microglial phagocytosis of dead or dying neurons can be beneficial by preventing the release of damaging and/or pro-inflammatory intracellular components. However, there is now evidence that under certain conditions, such as inflammation, microglia can also phagocytose viable neurons, thus executing their death. Such phagocytic cell death may result from exposure of phosphatidylserine (PS) or other eat-me signals on otherwise viable neurons as a result of physiological activation or sub-toxic insult, and neuronal phagocytosis by activated microglia. In this review, we discuss the mechanisms of phagocytic cell death and its potential roles in Alzheimer’s Disease, Parkinson’s Disease, and Frontotemporal Dementia. Frontiers Research Foundation 2012-02-28 /pmc/articles/PMC3288722/ /pubmed/22403545 http://dx.doi.org/10.3389/fphar.2012.00027 Text en Copyright © 2012 Neher, Neniskyte and Brown. http://www.frontiersin.org/licenseagreement This is an open-access article distributed under the terms of the Creative Commons Attribution Non Commercial License, which permits non-commercial use, distribution, and reproduction in other forums, provided the original authors and source are credited. |
spellingShingle | Pharmacology Neher, Jonas J. Neniskyte, Urte Brown, Guy C. Primary Phagocytosis of Neurons by Inflamed Microglia: Potential Roles in Neurodegeneration |
title | Primary Phagocytosis of Neurons by Inflamed Microglia: Potential Roles in Neurodegeneration |
title_full | Primary Phagocytosis of Neurons by Inflamed Microglia: Potential Roles in Neurodegeneration |
title_fullStr | Primary Phagocytosis of Neurons by Inflamed Microglia: Potential Roles in Neurodegeneration |
title_full_unstemmed | Primary Phagocytosis of Neurons by Inflamed Microglia: Potential Roles in Neurodegeneration |
title_short | Primary Phagocytosis of Neurons by Inflamed Microglia: Potential Roles in Neurodegeneration |
title_sort | primary phagocytosis of neurons by inflamed microglia: potential roles in neurodegeneration |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3288722/ https://www.ncbi.nlm.nih.gov/pubmed/22403545 http://dx.doi.org/10.3389/fphar.2012.00027 |
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