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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...

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Autores principales: Fliegert, Ralf, Riekehr, Winnie M., Guse, Andreas H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
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.
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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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