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Glial- and Neuronal-Specific Expression of CCL5 mRNA in the Rat Brain

Chemokine (C-C motif) ligand 5 (CCL5) belongs to a group of chemokines that play a role in the peripheral immune system, mostly as chemoattractant molecules, and mediate tactile allodynia. In the central nervous system (CNS), CCL5 and its receptors have multiple functions, including promoting neuroi...

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Autores principales: Lanfranco, Maria Fe, Mocchetti, Italo, Burns, Mark P., Villapol, Sonia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5770405/
https://www.ncbi.nlm.nih.gov/pubmed/29375328
http://dx.doi.org/10.3389/fnana.2017.00137
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author Lanfranco, Maria Fe
Mocchetti, Italo
Burns, Mark P.
Villapol, Sonia
author_facet Lanfranco, Maria Fe
Mocchetti, Italo
Burns, Mark P.
Villapol, Sonia
author_sort Lanfranco, Maria Fe
collection PubMed
description Chemokine (C-C motif) ligand 5 (CCL5) belongs to a group of chemokines that play a role in the peripheral immune system, mostly as chemoattractant molecules, and mediate tactile allodynia. In the central nervous system (CNS), CCL5 and its receptors have multiple functions, including promoting neuroinflammation, insulin signaling, neuromodulator of synaptic activity and neuroprotection against a variety of neurotoxins. Evidence has also suggested that this chemokine may regulate opioid response. The multifunctional profile of CCL5 might correlate with its ability to bind different chemokine receptors, as well as with its unique cellular expression. In this work, we have used fluorescence in situ hybridization combined with immunohistochemistry to examine the expression profile of CCL5 mRNA in the adult rat brain and provide evidence of its cellular localization. We have observed that the highest expression of CCL5 mRNA occurs in all major fiber tracts, including the corpus callosum, anterior commissure, and cerebral peduncle. In these tracts, CCL5 mRNA was localized in oligodendrocytes, astrocytes and microglia. Astrocytic and microglial expression was also evident in several brain areas including the cerebral cortex, caudate/putamen, hippocampus, and thalamus. Furthermore, using a specific neuronal marker, we observed CCL5 mRNA expression in discrete layers of the cortex and hippocampus. Interestingly, in the midbrain, CCL5 mRNA co-localized with tyrosine hydroxylase (TH) positive cells of the ventral tegmental area, suggesting that CCL5 might be expressed by a subset of dopaminergic neurons of the mesolimbic system. The expression of CCL5 mRNA and protein, together with its receptors, in selected brain cell populations proposes that this chemokine could be involved in neuronal/glial communication.
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spelling pubmed-57704052018-01-26 Glial- and Neuronal-Specific Expression of CCL5 mRNA in the Rat Brain Lanfranco, Maria Fe Mocchetti, Italo Burns, Mark P. Villapol, Sonia Front Neuroanat Neuroscience Chemokine (C-C motif) ligand 5 (CCL5) belongs to a group of chemokines that play a role in the peripheral immune system, mostly as chemoattractant molecules, and mediate tactile allodynia. In the central nervous system (CNS), CCL5 and its receptors have multiple functions, including promoting neuroinflammation, insulin signaling, neuromodulator of synaptic activity and neuroprotection against a variety of neurotoxins. Evidence has also suggested that this chemokine may regulate opioid response. The multifunctional profile of CCL5 might correlate with its ability to bind different chemokine receptors, as well as with its unique cellular expression. In this work, we have used fluorescence in situ hybridization combined with immunohistochemistry to examine the expression profile of CCL5 mRNA in the adult rat brain and provide evidence of its cellular localization. We have observed that the highest expression of CCL5 mRNA occurs in all major fiber tracts, including the corpus callosum, anterior commissure, and cerebral peduncle. In these tracts, CCL5 mRNA was localized in oligodendrocytes, astrocytes and microglia. Astrocytic and microglial expression was also evident in several brain areas including the cerebral cortex, caudate/putamen, hippocampus, and thalamus. Furthermore, using a specific neuronal marker, we observed CCL5 mRNA expression in discrete layers of the cortex and hippocampus. Interestingly, in the midbrain, CCL5 mRNA co-localized with tyrosine hydroxylase (TH) positive cells of the ventral tegmental area, suggesting that CCL5 might be expressed by a subset of dopaminergic neurons of the mesolimbic system. The expression of CCL5 mRNA and protein, together with its receptors, in selected brain cell populations proposes that this chemokine could be involved in neuronal/glial communication. Frontiers Media S.A. 2018-01-12 /pmc/articles/PMC5770405/ /pubmed/29375328 http://dx.doi.org/10.3389/fnana.2017.00137 Text en Copyright © 2018 Lanfranco, Moccheti, Burns and Villapol. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Lanfranco, Maria Fe
Mocchetti, Italo
Burns, Mark P.
Villapol, Sonia
Glial- and Neuronal-Specific Expression of CCL5 mRNA in the Rat Brain
title Glial- and Neuronal-Specific Expression of CCL5 mRNA in the Rat Brain
title_full Glial- and Neuronal-Specific Expression of CCL5 mRNA in the Rat Brain
title_fullStr Glial- and Neuronal-Specific Expression of CCL5 mRNA in the Rat Brain
title_full_unstemmed Glial- and Neuronal-Specific Expression of CCL5 mRNA in the Rat Brain
title_short Glial- and Neuronal-Specific Expression of CCL5 mRNA in the Rat Brain
title_sort glial- and neuronal-specific expression of ccl5 mrna in the rat brain
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5770405/
https://www.ncbi.nlm.nih.gov/pubmed/29375328
http://dx.doi.org/10.3389/fnana.2017.00137
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