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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2015
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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 |
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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 |
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