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A critical role for pannexin-1 in activation of innate immune cells of the choroid plexus

Epiplexus cells are a population of innate immune cells in the choroid plexus of the brain ventricles. They are thought to contribute to the immune component of the blood-cerebrospinal-fluid-barrier (BCSFB). Here we have developed a novel technique for studying epiplexus cells in acutely isolated, l...

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Autores principales: Maslieieva, Valentyna, Thompson, Roger J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4048302/
https://www.ncbi.nlm.nih.gov/pubmed/24418937
http://dx.doi.org/10.4161/chan.27653
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author Maslieieva, Valentyna
Thompson, Roger J
author_facet Maslieieva, Valentyna
Thompson, Roger J
author_sort Maslieieva, Valentyna
collection PubMed
description Epiplexus cells are a population of innate immune cells in the choroid plexus of the brain ventricles. They are thought to contribute to the immune component of the blood-cerebrospinal-fluid-barrier (BCSFB). Here we have developed a novel technique for studying epiplexus cells in acutely isolated, live and intact choroid plexus. We show that epiplexus cells are potently activated by exogenous ATP, increasing their motility within the tissue. This ATP-induced chemokinesis required activation of pannexin-1 channels, which are expressed by the epithelial cells of the choroid plexus and not the epiplexus cells themselves. Furthermore, ATP acts at least in part through the P2X4 ionotropic purinergic receptor. Thus, the resident immune cells of the choroid plexus appear to be in communication with the epithelial cells through pannexin-1 channels.
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spelling pubmed-40483022015-03-01 A critical role for pannexin-1 in activation of innate immune cells of the choroid plexus Maslieieva, Valentyna Thompson, Roger J Channels (Austin) Research Paper Epiplexus cells are a population of innate immune cells in the choroid plexus of the brain ventricles. They are thought to contribute to the immune component of the blood-cerebrospinal-fluid-barrier (BCSFB). Here we have developed a novel technique for studying epiplexus cells in acutely isolated, live and intact choroid plexus. We show that epiplexus cells are potently activated by exogenous ATP, increasing their motility within the tissue. This ATP-induced chemokinesis required activation of pannexin-1 channels, which are expressed by the epithelial cells of the choroid plexus and not the epiplexus cells themselves. Furthermore, ATP acts at least in part through the P2X4 ionotropic purinergic receptor. Thus, the resident immune cells of the choroid plexus appear to be in communication with the epithelial cells through pannexin-1 channels. Landes Bioscience 2014-03-01 2014-01-13 /pmc/articles/PMC4048302/ /pubmed/24418937 http://dx.doi.org/10.4161/chan.27653 Text en Copyright © 2014 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Research Paper
Maslieieva, Valentyna
Thompson, Roger J
A critical role for pannexin-1 in activation of innate immune cells of the choroid plexus
title A critical role for pannexin-1 in activation of innate immune cells of the choroid plexus
title_full A critical role for pannexin-1 in activation of innate immune cells of the choroid plexus
title_fullStr A critical role for pannexin-1 in activation of innate immune cells of the choroid plexus
title_full_unstemmed A critical role for pannexin-1 in activation of innate immune cells of the choroid plexus
title_short A critical role for pannexin-1 in activation of innate immune cells of the choroid plexus
title_sort critical role for pannexin-1 in activation of innate immune cells of the choroid plexus
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4048302/
https://www.ncbi.nlm.nih.gov/pubmed/24418937
http://dx.doi.org/10.4161/chan.27653
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