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Inhibition of TRPP3 by calmodulin through Ca(2+)/calmodulin-dependent protein kinase II

Transient receptor potential (TRP) polycystin-3 (TRPP3) is a non-selective cation channel activated by Ca(2+) and protons and is involved in regulating ciliary Ca(2+) concentration, hedgehog signaling and sour tasting. The TRPP3 channel function and regulation are still not well understood. Here we...

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Detalles Bibliográficos
Autores principales: Liu, Xiong, Wang, Yifang, Weng, Ziyi, Xu, Qinyi, Zhou, Cefan, Tang, JingFeng, Chen, Xing-Zhen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10134200/
https://www.ncbi.nlm.nih.gov/pubmed/37193065
http://dx.doi.org/10.1016/j.cellin.2023.100088
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author Liu, Xiong
Wang, Yifang
Weng, Ziyi
Xu, Qinyi
Zhou, Cefan
Tang, JingFeng
Chen, Xing-Zhen
author_facet Liu, Xiong
Wang, Yifang
Weng, Ziyi
Xu, Qinyi
Zhou, Cefan
Tang, JingFeng
Chen, Xing-Zhen
author_sort Liu, Xiong
collection PubMed
description Transient receptor potential (TRP) polycystin-3 (TRPP3) is a non-selective cation channel activated by Ca(2+) and protons and is involved in regulating ciliary Ca(2+) concentration, hedgehog signaling and sour tasting. The TRPP3 channel function and regulation are still not well understood. Here we investigated regulation of TRPP3 by calmodulin (CaM) by means of electrophysiology and Xenopus oocytes as an expression model. We found that TRPP3 channel function is enhanced by calmidazolium, a CaM antagonist, and inhibited by CaM through binding of the CaM N-lobe to a TRPP3 C-terminal domain not overlapped with the EF-hand. We further revealed that the TRPP3/CaM interaction promotes phosphorylation of TRPP3 at threonine 591 by Ca(2+)/CaM-dependent protein kinase II, which mediates the inhibition of TRPP3 by CaM.
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spelling pubmed-101342002023-05-15 Inhibition of TRPP3 by calmodulin through Ca(2+)/calmodulin-dependent protein kinase II Liu, Xiong Wang, Yifang Weng, Ziyi Xu, Qinyi Zhou, Cefan Tang, JingFeng Chen, Xing-Zhen Cell Insight Research Article Transient receptor potential (TRP) polycystin-3 (TRPP3) is a non-selective cation channel activated by Ca(2+) and protons and is involved in regulating ciliary Ca(2+) concentration, hedgehog signaling and sour tasting. The TRPP3 channel function and regulation are still not well understood. Here we investigated regulation of TRPP3 by calmodulin (CaM) by means of electrophysiology and Xenopus oocytes as an expression model. We found that TRPP3 channel function is enhanced by calmidazolium, a CaM antagonist, and inhibited by CaM through binding of the CaM N-lobe to a TRPP3 C-terminal domain not overlapped with the EF-hand. We further revealed that the TRPP3/CaM interaction promotes phosphorylation of TRPP3 at threonine 591 by Ca(2+)/CaM-dependent protein kinase II, which mediates the inhibition of TRPP3 by CaM. Elsevier 2023-02-09 /pmc/articles/PMC10134200/ /pubmed/37193065 http://dx.doi.org/10.1016/j.cellin.2023.100088 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Liu, Xiong
Wang, Yifang
Weng, Ziyi
Xu, Qinyi
Zhou, Cefan
Tang, JingFeng
Chen, Xing-Zhen
Inhibition of TRPP3 by calmodulin through Ca(2+)/calmodulin-dependent protein kinase II
title Inhibition of TRPP3 by calmodulin through Ca(2+)/calmodulin-dependent protein kinase II
title_full Inhibition of TRPP3 by calmodulin through Ca(2+)/calmodulin-dependent protein kinase II
title_fullStr Inhibition of TRPP3 by calmodulin through Ca(2+)/calmodulin-dependent protein kinase II
title_full_unstemmed Inhibition of TRPP3 by calmodulin through Ca(2+)/calmodulin-dependent protein kinase II
title_short Inhibition of TRPP3 by calmodulin through Ca(2+)/calmodulin-dependent protein kinase II
title_sort inhibition of trpp3 by calmodulin through ca(2+)/calmodulin-dependent protein kinase ii
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10134200/
https://www.ncbi.nlm.nih.gov/pubmed/37193065
http://dx.doi.org/10.1016/j.cellin.2023.100088
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