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Dark microglia: Why are they dark?
Using transmission electron microscopy (TEM) we recently characterized a microglial phenotype that is induced by chronic stress, fractalkine receptor deficiency, aging, or Alzheimer disease pathology. These ‘dark’ microglia appear overly active compared with the normal microglia, reaching for synapt...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5193044/ https://www.ncbi.nlm.nih.gov/pubmed/28042375 http://dx.doi.org/10.1080/19420889.2016.1230575 |
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author | Bisht, Kanchan Sharma, Kaushik Lacoste, Baptiste Tremblay, Marie-Ève |
author_facet | Bisht, Kanchan Sharma, Kaushik Lacoste, Baptiste Tremblay, Marie-Ève |
author_sort | Bisht, Kanchan |
collection | PubMed |
description | Using transmission electron microscopy (TEM) we recently characterized a microglial phenotype that is induced by chronic stress, fractalkine receptor deficiency, aging, or Alzheimer disease pathology. These ‘dark’ microglia appear overly active compared with the normal microglia, reaching for synaptic clefts, and extensively engulfing pre-synaptic axon terminals and post-synaptic dendritic spines. From these findings we hypothesized that dark microglia could be specifically implicated in the pathological remodeling of neuronal circuits, which impairs learning, memory, and other essential cognitive functions. In the present addendum we further discuss about the possible causes of their dark appearance under TEM. |
format | Online Article Text |
id | pubmed-5193044 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-51930442016-12-30 Dark microglia: Why are they dark? Bisht, Kanchan Sharma, Kaushik Lacoste, Baptiste Tremblay, Marie-Ève Commun Integr Biol Article Addendum Using transmission electron microscopy (TEM) we recently characterized a microglial phenotype that is induced by chronic stress, fractalkine receptor deficiency, aging, or Alzheimer disease pathology. These ‘dark’ microglia appear overly active compared with the normal microglia, reaching for synaptic clefts, and extensively engulfing pre-synaptic axon terminals and post-synaptic dendritic spines. From these findings we hypothesized that dark microglia could be specifically implicated in the pathological remodeling of neuronal circuits, which impairs learning, memory, and other essential cognitive functions. In the present addendum we further discuss about the possible causes of their dark appearance under TEM. Taylor & Francis 2016-10-03 /pmc/articles/PMC5193044/ /pubmed/28042375 http://dx.doi.org/10.1080/19420889.2016.1230575 Text en © 2016 The Author(s). Published with license by Taylor & Francis. This is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted. |
spellingShingle | Article Addendum Bisht, Kanchan Sharma, Kaushik Lacoste, Baptiste Tremblay, Marie-Ève Dark microglia: Why are they dark? |
title | Dark microglia: Why are they dark? |
title_full | Dark microglia: Why are they dark? |
title_fullStr | Dark microglia: Why are they dark? |
title_full_unstemmed | Dark microglia: Why are they dark? |
title_short | Dark microglia: Why are they dark? |
title_sort | dark microglia: why are they dark? |
topic | Article Addendum |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5193044/ https://www.ncbi.nlm.nih.gov/pubmed/28042375 http://dx.doi.org/10.1080/19420889.2016.1230575 |
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