Cargando…
Microglial displacement of inhibitory synapses provides neuroprotection in the adult brain
Microglia actively survey the brain microenvironment and play essential roles in sculpting synaptic connections during brain development. While microglial functions in the adult brain are less clear, activated microglia can closely appose neuronal cell bodies and displace axosomatic presynaptic term...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Pub. Group
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4109015/ https://www.ncbi.nlm.nih.gov/pubmed/25047355 http://dx.doi.org/10.1038/ncomms5486 |
_version_ | 1782327824763322368 |
---|---|
author | Chen, Zhihong Jalabi, Walid Hu, Weiwei Park, Hyun-Joo Gale, John T. Kidd, Grahame J. Bernatowicz, Rodica Gossman, Zachary C. Chen, Jacqueline T. Dutta, Ranjan Trapp, Bruce D. |
author_facet | Chen, Zhihong Jalabi, Walid Hu, Weiwei Park, Hyun-Joo Gale, John T. Kidd, Grahame J. Bernatowicz, Rodica Gossman, Zachary C. Chen, Jacqueline T. Dutta, Ranjan Trapp, Bruce D. |
author_sort | Chen, Zhihong |
collection | PubMed |
description | Microglia actively survey the brain microenvironment and play essential roles in sculpting synaptic connections during brain development. While microglial functions in the adult brain are less clear, activated microglia can closely appose neuronal cell bodies and displace axosomatic presynaptic terminals. Microglia-mediated stripping of presynaptic terminals is considered neuroprotective, but the cellular and molecular mechanisms are poorly defined. Using 3D electron microscopy, we demonstrate that activated microglia displace inhibitory presynaptic terminals from cortical neurons in adult mice. Electrophysiological recordings further establish that the reduction in inhibitory GABAergic synapses increased synchronized firing of cortical neurons in γ-frequency band. Increased neuronal activity results in the calcium-mediated activation of CaM kinase IV, phosphorylation of CREB, increased expression of antiapoptotic and neurotrophic molecules and reduced apoptosis of cortical neurons following injury. These results indicate that activated microglia can protect the adult brain by migrating to inhibitory synapses and displacing them from cortical neurons. |
format | Online Article Text |
id | pubmed-4109015 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Pub. Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-41090152014-08-15 Microglial displacement of inhibitory synapses provides neuroprotection in the adult brain Chen, Zhihong Jalabi, Walid Hu, Weiwei Park, Hyun-Joo Gale, John T. Kidd, Grahame J. Bernatowicz, Rodica Gossman, Zachary C. Chen, Jacqueline T. Dutta, Ranjan Trapp, Bruce D. Nat Commun Article Microglia actively survey the brain microenvironment and play essential roles in sculpting synaptic connections during brain development. While microglial functions in the adult brain are less clear, activated microglia can closely appose neuronal cell bodies and displace axosomatic presynaptic terminals. Microglia-mediated stripping of presynaptic terminals is considered neuroprotective, but the cellular and molecular mechanisms are poorly defined. Using 3D electron microscopy, we demonstrate that activated microglia displace inhibitory presynaptic terminals from cortical neurons in adult mice. Electrophysiological recordings further establish that the reduction in inhibitory GABAergic synapses increased synchronized firing of cortical neurons in γ-frequency band. Increased neuronal activity results in the calcium-mediated activation of CaM kinase IV, phosphorylation of CREB, increased expression of antiapoptotic and neurotrophic molecules and reduced apoptosis of cortical neurons following injury. These results indicate that activated microglia can protect the adult brain by migrating to inhibitory synapses and displacing them from cortical neurons. Nature Pub. Group 2014-07-22 /pmc/articles/PMC4109015/ /pubmed/25047355 http://dx.doi.org/10.1038/ncomms5486 Text en Copyright © 2014, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Chen, Zhihong Jalabi, Walid Hu, Weiwei Park, Hyun-Joo Gale, John T. Kidd, Grahame J. Bernatowicz, Rodica Gossman, Zachary C. Chen, Jacqueline T. Dutta, Ranjan Trapp, Bruce D. Microglial displacement of inhibitory synapses provides neuroprotection in the adult brain |
title | Microglial displacement of inhibitory synapses provides neuroprotection in the adult brain |
title_full | Microglial displacement of inhibitory synapses provides neuroprotection in the adult brain |
title_fullStr | Microglial displacement of inhibitory synapses provides neuroprotection in the adult brain |
title_full_unstemmed | Microglial displacement of inhibitory synapses provides neuroprotection in the adult brain |
title_short | Microglial displacement of inhibitory synapses provides neuroprotection in the adult brain |
title_sort | microglial displacement of inhibitory synapses provides neuroprotection in the adult brain |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4109015/ https://www.ncbi.nlm.nih.gov/pubmed/25047355 http://dx.doi.org/10.1038/ncomms5486 |
work_keys_str_mv | AT chenzhihong microglialdisplacementofinhibitorysynapsesprovidesneuroprotectionintheadultbrain AT jalabiwalid microglialdisplacementofinhibitorysynapsesprovidesneuroprotectionintheadultbrain AT huweiwei microglialdisplacementofinhibitorysynapsesprovidesneuroprotectionintheadultbrain AT parkhyunjoo microglialdisplacementofinhibitorysynapsesprovidesneuroprotectionintheadultbrain AT galejohnt microglialdisplacementofinhibitorysynapsesprovidesneuroprotectionintheadultbrain AT kiddgrahamej microglialdisplacementofinhibitorysynapsesprovidesneuroprotectionintheadultbrain AT bernatowiczrodica microglialdisplacementofinhibitorysynapsesprovidesneuroprotectionintheadultbrain AT gossmanzacharyc microglialdisplacementofinhibitorysynapsesprovidesneuroprotectionintheadultbrain AT chenjacquelinet microglialdisplacementofinhibitorysynapsesprovidesneuroprotectionintheadultbrain AT duttaranjan microglialdisplacementofinhibitorysynapsesprovidesneuroprotectionintheadultbrain AT trappbruced microglialdisplacementofinhibitorysynapsesprovidesneuroprotectionintheadultbrain |