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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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.
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