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Does Cyclic ADP-Ribose (cADPR) Activate the Non-selective Cation Channel TRPM2?
TRPM2 is a non-selective, Ca(2+)-permeable cation channel widely expressed in immune cells. It is firmly established that the channel can be activated by intracellular adenosine 5′-diphosphoribose (ADPR). Until recent cryo-EM structures have exhibited an additional nucleotide binding site in the N-t...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7438885/ https://www.ncbi.nlm.nih.gov/pubmed/32903769 http://dx.doi.org/10.3389/fimmu.2020.02018 |
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author | Fliegert, Ralf Riekehr, Winnie M. Guse, Andreas H. |
author_facet | Fliegert, Ralf Riekehr, Winnie M. Guse, Andreas H. |
author_sort | Fliegert, Ralf |
collection | PubMed |
description | TRPM2 is a non-selective, Ca(2+)-permeable cation channel widely expressed in immune cells. It is firmly established that the channel can be activated by intracellular adenosine 5′-diphosphoribose (ADPR). Until recent cryo-EM structures have exhibited an additional nucleotide binding site in the N-terminus of the channel, this activation was thought to occur via binding to a C-terminal domain of the channel that is highly homologous to the ADPR pyrophosphatase NudT9. Over the years it has been controversially discussed whether the Ca(2+) mobilizing second messenger cyclic ADP ribose (cADPR) might also directly activate Ca(2+) entry via TRPM2. Here we will review the status of this discussion. |
format | Online Article Text |
id | pubmed-7438885 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-74388852020-09-03 Does Cyclic ADP-Ribose (cADPR) Activate the Non-selective Cation Channel TRPM2? Fliegert, Ralf Riekehr, Winnie M. Guse, Andreas H. Front Immunol Immunology TRPM2 is a non-selective, Ca(2+)-permeable cation channel widely expressed in immune cells. It is firmly established that the channel can be activated by intracellular adenosine 5′-diphosphoribose (ADPR). Until recent cryo-EM structures have exhibited an additional nucleotide binding site in the N-terminus of the channel, this activation was thought to occur via binding to a C-terminal domain of the channel that is highly homologous to the ADPR pyrophosphatase NudT9. Over the years it has been controversially discussed whether the Ca(2+) mobilizing second messenger cyclic ADP ribose (cADPR) might also directly activate Ca(2+) entry via TRPM2. Here we will review the status of this discussion. Frontiers Media S.A. 2020-08-11 /pmc/articles/PMC7438885/ /pubmed/32903769 http://dx.doi.org/10.3389/fimmu.2020.02018 Text en Copyright © 2020 Fliegert, Riekehr and Guse. 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) and the copyright owner(s) 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 Fliegert, Ralf Riekehr, Winnie M. Guse, Andreas H. Does Cyclic ADP-Ribose (cADPR) Activate the Non-selective Cation Channel TRPM2? |
title | Does Cyclic ADP-Ribose (cADPR) Activate the Non-selective Cation Channel TRPM2? |
title_full | Does Cyclic ADP-Ribose (cADPR) Activate the Non-selective Cation Channel TRPM2? |
title_fullStr | Does Cyclic ADP-Ribose (cADPR) Activate the Non-selective Cation Channel TRPM2? |
title_full_unstemmed | Does Cyclic ADP-Ribose (cADPR) Activate the Non-selective Cation Channel TRPM2? |
title_short | Does Cyclic ADP-Ribose (cADPR) Activate the Non-selective Cation Channel TRPM2? |
title_sort | does cyclic adp-ribose (cadpr) activate the non-selective cation channel trpm2? |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7438885/ https://www.ncbi.nlm.nih.gov/pubmed/32903769 http://dx.doi.org/10.3389/fimmu.2020.02018 |
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