Cargando…

P2X7 on Mouse T Cells: One Channel, Many Functions

The P2X7 receptor is an adenosine triphosphate (ATP)-gated cation channel that is expressed by several cells of the immune system. P2X7 is best known for its proinflammatory role in promoting inflammasome formation and release of mature interleukin (IL)-1β by innate immune cells. Mounting evidence i...

Descripción completa

Detalles Bibliográficos
Autores principales: Rissiek, Björn, Haag, Friedrich, Boyer, Olivier, Koch-Nolte, Friedrich, Adriouch, Sahil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4436801/
https://www.ncbi.nlm.nih.gov/pubmed/26042119
http://dx.doi.org/10.3389/fimmu.2015.00204
_version_ 1782372133851103232
author Rissiek, Björn
Haag, Friedrich
Boyer, Olivier
Koch-Nolte, Friedrich
Adriouch, Sahil
author_facet Rissiek, Björn
Haag, Friedrich
Boyer, Olivier
Koch-Nolte, Friedrich
Adriouch, Sahil
author_sort Rissiek, Björn
collection PubMed
description The P2X7 receptor is an adenosine triphosphate (ATP)-gated cation channel that is expressed by several cells of the immune system. P2X7 is best known for its proinflammatory role in promoting inflammasome formation and release of mature interleukin (IL)-1β by innate immune cells. Mounting evidence indicates that P2X7 is also an important regulatory receptor of murine and human T cell functions. Murine T cells express a sensitive splice variant of P2X7 that can be activated either by non-covalent binding of ATP or, in the presence of nicotinamide adenine dinucleotide, by its covalent ADP-ribosylation catalyzed by the ecto-ADP-ribosyltransferase ARTC2.2. Prolonged activation of P2X7 by either one of these pathways triggers the induction of T cell death. Conversely, lower concentrations of ATP can activate P2X7 to enhance T cell proliferation and production of IL-2. In this review, we will highlight the molecular and cellular consequences of P2X7 activation on mouse T cells and its versatile role in T cell homeostasis and activation. Further, we will discuss important differences in the function of P2X7 on human and murine T cells.
format Online
Article
Text
id pubmed-4436801
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-44368012015-06-03 P2X7 on Mouse T Cells: One Channel, Many Functions Rissiek, Björn Haag, Friedrich Boyer, Olivier Koch-Nolte, Friedrich Adriouch, Sahil Front Immunol Immunology The P2X7 receptor is an adenosine triphosphate (ATP)-gated cation channel that is expressed by several cells of the immune system. P2X7 is best known for its proinflammatory role in promoting inflammasome formation and release of mature interleukin (IL)-1β by innate immune cells. Mounting evidence indicates that P2X7 is also an important regulatory receptor of murine and human T cell functions. Murine T cells express a sensitive splice variant of P2X7 that can be activated either by non-covalent binding of ATP or, in the presence of nicotinamide adenine dinucleotide, by its covalent ADP-ribosylation catalyzed by the ecto-ADP-ribosyltransferase ARTC2.2. Prolonged activation of P2X7 by either one of these pathways triggers the induction of T cell death. Conversely, lower concentrations of ATP can activate P2X7 to enhance T cell proliferation and production of IL-2. In this review, we will highlight the molecular and cellular consequences of P2X7 activation on mouse T cells and its versatile role in T cell homeostasis and activation. Further, we will discuss important differences in the function of P2X7 on human and murine T cells. Frontiers Media S.A. 2015-05-19 /pmc/articles/PMC4436801/ /pubmed/26042119 http://dx.doi.org/10.3389/fimmu.2015.00204 Text en Copyright © 2015 Rissiek, Haag, Boyer, Koch-Nolte and Adriouch. 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 Immunology
Rissiek, Björn
Haag, Friedrich
Boyer, Olivier
Koch-Nolte, Friedrich
Adriouch, Sahil
P2X7 on Mouse T Cells: One Channel, Many Functions
title P2X7 on Mouse T Cells: One Channel, Many Functions
title_full P2X7 on Mouse T Cells: One Channel, Many Functions
title_fullStr P2X7 on Mouse T Cells: One Channel, Many Functions
title_full_unstemmed P2X7 on Mouse T Cells: One Channel, Many Functions
title_short P2X7 on Mouse T Cells: One Channel, Many Functions
title_sort p2x7 on mouse t cells: one channel, many functions
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4436801/
https://www.ncbi.nlm.nih.gov/pubmed/26042119
http://dx.doi.org/10.3389/fimmu.2015.00204
work_keys_str_mv AT rissiekbjorn p2x7onmousetcellsonechannelmanyfunctions
AT haagfriedrich p2x7onmousetcellsonechannelmanyfunctions
AT boyerolivier p2x7onmousetcellsonechannelmanyfunctions
AT kochnoltefriedrich p2x7onmousetcellsonechannelmanyfunctions
AT adriouchsahil p2x7onmousetcellsonechannelmanyfunctions