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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 |
Publicado: |
Frontiers Media S.A.
2020
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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 |
Sumario: | 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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