Cargando…

Spinal microglial motility is independent of neuronal activity and plasticity in adult mice

Microglia are the resident macrophages in the central nervous system. In the spinal cord dorsal horn, microglia stay in resting condition during physiological sensory processing, and are activated under pathological conditions such as peripheral nerve injury. In cases such as this, the nearby restin...

Descripción completa

Detalles Bibliográficos
Autores principales: Chen, Tao, Koga, Kohei, Li, Xiang-Yao, Zhuo, Min
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2857828/
https://www.ncbi.nlm.nih.gov/pubmed/20380706
http://dx.doi.org/10.1186/1744-8069-6-19
_version_ 1782180346821869568
author Chen, Tao
Koga, Kohei
Li, Xiang-Yao
Zhuo, Min
author_facet Chen, Tao
Koga, Kohei
Li, Xiang-Yao
Zhuo, Min
author_sort Chen, Tao
collection PubMed
description Microglia are the resident macrophages in the central nervous system. In the spinal cord dorsal horn, microglia stay in resting condition during physiological sensory processing, and are activated under pathological conditions such as peripheral nerve injury. In cases such as this, the nearby resting microglia increase their motility and accumulate at the site of injury. However, direct evidence to support that nerve activity can enhance the motility of microglia has not yet to be reported. In this study we investigated whether the activation of spinal microglia under in vivo nerve injury may be mimicked by neuronal activity in the spinal cord slice preparation. We found that local application of spinal excitatory neurotransmitters, such as glutamate and substance P did not cause any change in the motility of microglial cells in the spinal cord dorsal horn. The motility of microglial cells is unlikely modulated by other transmitters, neuromodulators and chemokines, because similar applications such as GABA, serotonin, noradrenaline, carbachol, fractalkine or interleukin did not produce any obvious effect. Furthermore, low or high frequency stimulation of spinal dorsal root fibers at noxious intensities failed to cause any enhanced extension or retraction of the microglia processes. By contrast, focal application of ATP triggered rapid and robust activation of microglial cells in the spinal dorsal horn. Our results provide the first evidence that the activation of microglia in the spinal cord after nerve injury is unlikely due solely to neuronal activity, non-neuronal factors are likely responsible for the activation of nerve injury-related microglial cells in the spinal dorsal horn.
format Text
id pubmed-2857828
institution National Center for Biotechnology Information
language English
publishDate 2010
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-28578282010-04-22 Spinal microglial motility is independent of neuronal activity and plasticity in adult mice Chen, Tao Koga, Kohei Li, Xiang-Yao Zhuo, Min Mol Pain Research Microglia are the resident macrophages in the central nervous system. In the spinal cord dorsal horn, microglia stay in resting condition during physiological sensory processing, and are activated under pathological conditions such as peripheral nerve injury. In cases such as this, the nearby resting microglia increase their motility and accumulate at the site of injury. However, direct evidence to support that nerve activity can enhance the motility of microglia has not yet to be reported. In this study we investigated whether the activation of spinal microglia under in vivo nerve injury may be mimicked by neuronal activity in the spinal cord slice preparation. We found that local application of spinal excitatory neurotransmitters, such as glutamate and substance P did not cause any change in the motility of microglial cells in the spinal cord dorsal horn. The motility of microglial cells is unlikely modulated by other transmitters, neuromodulators and chemokines, because similar applications such as GABA, serotonin, noradrenaline, carbachol, fractalkine or interleukin did not produce any obvious effect. Furthermore, low or high frequency stimulation of spinal dorsal root fibers at noxious intensities failed to cause any enhanced extension or retraction of the microglia processes. By contrast, focal application of ATP triggered rapid and robust activation of microglial cells in the spinal dorsal horn. Our results provide the first evidence that the activation of microglia in the spinal cord after nerve injury is unlikely due solely to neuronal activity, non-neuronal factors are likely responsible for the activation of nerve injury-related microglial cells in the spinal dorsal horn. BioMed Central 2010-04-09 /pmc/articles/PMC2857828/ /pubmed/20380706 http://dx.doi.org/10.1186/1744-8069-6-19 Text en Copyright ©2010 Chen et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Chen, Tao
Koga, Kohei
Li, Xiang-Yao
Zhuo, Min
Spinal microglial motility is independent of neuronal activity and plasticity in adult mice
title Spinal microglial motility is independent of neuronal activity and plasticity in adult mice
title_full Spinal microglial motility is independent of neuronal activity and plasticity in adult mice
title_fullStr Spinal microglial motility is independent of neuronal activity and plasticity in adult mice
title_full_unstemmed Spinal microglial motility is independent of neuronal activity and plasticity in adult mice
title_short Spinal microglial motility is independent of neuronal activity and plasticity in adult mice
title_sort spinal microglial motility is independent of neuronal activity and plasticity in adult mice
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2857828/
https://www.ncbi.nlm.nih.gov/pubmed/20380706
http://dx.doi.org/10.1186/1744-8069-6-19
work_keys_str_mv AT chentao spinalmicroglialmotilityisindependentofneuronalactivityandplasticityinadultmice
AT kogakohei spinalmicroglialmotilityisindependentofneuronalactivityandplasticityinadultmice
AT lixiangyao spinalmicroglialmotilityisindependentofneuronalactivityandplasticityinadultmice
AT zhuomin spinalmicroglialmotilityisindependentofneuronalactivityandplasticityinadultmice