CXCL12 chemokine and GABA neurotransmitter systems crosstalk and their putative roles

Since CXCL12 and its receptors, CXCR4 and CXCR7, have been found in the brain, the role of this chemokine has been expanded from chemoattractant in the immune system to neuromodulatory in the brain. Several pieces of evidence suggest that this chemokine system could crosstalk with the GABAergic syst...

Full description

Bibliographic Details
Main Author: Guyon eAlice
Format: Article
Language:English
Published: Frontiers Media S.A. 2014-04-01
Series:Frontiers in Cellular Neuroscience
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fncel.2014.00115/full
_version_ 1818921740846235648
author Guyon eAlice
author_facet Guyon eAlice
author_sort Guyon eAlice
collection DOAJ
description Since CXCL12 and its receptors, CXCR4 and CXCR7, have been found in the brain, the role of this chemokine has been expanded from chemoattractant in the immune system to neuromodulatory in the brain. Several pieces of evidence suggest that this chemokine system could crosstalk with the GABAergic system, known to be the main inhibitory neurotransmitter system in the brain. <br/>Indeed, GABA and CXCL12 as well as their receptors are colocalized in many cell types including neurons and there are several examples in which these two systems interact. Several mechanisms can be proposed to explain how these systems interact, including receptor-receptor interactions, crosstalk at the level of second messenger cascades, or direct pharmacological interactions, as GABA and GABAB receptor agonists/antagonists have been shown to be allosteric modulators of CXCR4.<br/>The interplay between CXCL12/CXCR4-CXCR7 and GABA/GABAA-GABAB receptors systems could have many physiological implications in neurotransmission, cancer and inflammation. In addition, the GABAB agonist baclofen is currently used in medicine to treat spasticity in patients with spinal cord injury, cerebral palsy, traumatic brain injury, multiple sclerosis and other disorders. More recently it has also been used in the treatment of alcohol dependence and withdrawal. The allosteric effects of this agent on CXCR4 could contribute to these beneficial effects or at the opposite, to its side effects.<br/><br/>
first_indexed 2024-12-20T01:42:27Z
format Article
id doaj.art-109f155b244f4f479ff5be300c6adb81
institution Directory Open Access Journal
issn 1662-5102
language English
last_indexed 2024-12-20T01:42:27Z
publishDate 2014-04-01
publisher Frontiers Media S.A.
record_format Article
series Frontiers in Cellular Neuroscience
spelling doaj.art-109f155b244f4f479ff5be300c6adb812022-12-21T19:57:52ZengFrontiers Media S.A.Frontiers in Cellular Neuroscience1662-51022014-04-01810.3389/fncel.2014.0011587968CXCL12 chemokine and GABA neurotransmitter systems crosstalk and their putative rolesGuyon eAlice0CNRS-UNSASince CXCL12 and its receptors, CXCR4 and CXCR7, have been found in the brain, the role of this chemokine has been expanded from chemoattractant in the immune system to neuromodulatory in the brain. Several pieces of evidence suggest that this chemokine system could crosstalk with the GABAergic system, known to be the main inhibitory neurotransmitter system in the brain. <br/>Indeed, GABA and CXCL12 as well as their receptors are colocalized in many cell types including neurons and there are several examples in which these two systems interact. Several mechanisms can be proposed to explain how these systems interact, including receptor-receptor interactions, crosstalk at the level of second messenger cascades, or direct pharmacological interactions, as GABA and GABAB receptor agonists/antagonists have been shown to be allosteric modulators of CXCR4.<br/>The interplay between CXCL12/CXCR4-CXCR7 and GABA/GABAA-GABAB receptors systems could have many physiological implications in neurotransmission, cancer and inflammation. In addition, the GABAB agonist baclofen is currently used in medicine to treat spasticity in patients with spinal cord injury, cerebral palsy, traumatic brain injury, multiple sclerosis and other disorders. More recently it has also been used in the treatment of alcohol dependence and withdrawal. The allosteric effects of this agent on CXCR4 could contribute to these beneficial effects or at the opposite, to its side effects.<br/><br/>http://journal.frontiersin.org/Journal/10.3389/fncel.2014.00115/fullBaclofenCXCR4GABAGABAA receptorsGABAB receptorsCXCR7
spellingShingle Guyon eAlice
CXCL12 chemokine and GABA neurotransmitter systems crosstalk and their putative roles
Frontiers in Cellular Neuroscience
Baclofen
CXCR4
GABA
GABAA receptors
GABAB receptors
CXCR7
title CXCL12 chemokine and GABA neurotransmitter systems crosstalk and their putative roles
title_full CXCL12 chemokine and GABA neurotransmitter systems crosstalk and their putative roles
title_fullStr CXCL12 chemokine and GABA neurotransmitter systems crosstalk and their putative roles
title_full_unstemmed CXCL12 chemokine and GABA neurotransmitter systems crosstalk and their putative roles
title_short CXCL12 chemokine and GABA neurotransmitter systems crosstalk and their putative roles
title_sort cxcl12 chemokine and gaba neurotransmitter systems crosstalk and their putative roles
topic Baclofen
CXCR4
GABA
GABAA receptors
GABAB receptors
CXCR7
url http://journal.frontiersin.org/Journal/10.3389/fncel.2014.00115/full
work_keys_str_mv AT guyonealice cxcl12chemokineandgabaneurotransmittersystemscrosstalkandtheirputativeroles