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Transient receptor potential channels meet phosphoinositides

Transient receptor potential (TRP) cation channels are unique cellular sensors that are involved in multiple cellular functions, ranging from transduction of sensory signals to the regulation of Ca(2+) and Mg(2+) homoeostasis. Malfunctioning of TRP channels is now recognized as the cause of several...

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Detalles Bibliográficos
Autores principales: Nilius, Bernd, Owsianik, Grzegorz, Voets, Thomas
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2570475/
https://www.ncbi.nlm.nih.gov/pubmed/18923420
http://dx.doi.org/10.1038/emboj.2008.217
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author Nilius, Bernd
Owsianik, Grzegorz
Voets, Thomas
author_facet Nilius, Bernd
Owsianik, Grzegorz
Voets, Thomas
author_sort Nilius, Bernd
collection PubMed
description Transient receptor potential (TRP) cation channels are unique cellular sensors that are involved in multiple cellular functions, ranging from transduction of sensory signals to the regulation of Ca(2+) and Mg(2+) homoeostasis. Malfunctioning of TRP channels is now recognized as the cause of several hereditary and acquired human diseases. At the time of cloning of the first Drosophila TRP channel, a close connection between gating and phosphatidylinositol phosphates (PIPs) was already recognized. In this review, we summarize current knowledge about the mechanisms of interaction between TRP channels and PIPs, and discuss the possible functional implications of TRP–PIP interactions to human physiology and pathophysiology.
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spelling pubmed-25704752008-11-07 Transient receptor potential channels meet phosphoinositides Nilius, Bernd Owsianik, Grzegorz Voets, Thomas EMBO J New EMBO Member's Review Transient receptor potential (TRP) cation channels are unique cellular sensors that are involved in multiple cellular functions, ranging from transduction of sensory signals to the regulation of Ca(2+) and Mg(2+) homoeostasis. Malfunctioning of TRP channels is now recognized as the cause of several hereditary and acquired human diseases. At the time of cloning of the first Drosophila TRP channel, a close connection between gating and phosphatidylinositol phosphates (PIPs) was already recognized. In this review, we summarize current knowledge about the mechanisms of interaction between TRP channels and PIPs, and discuss the possible functional implications of TRP–PIP interactions to human physiology and pathophysiology. Nature Publishing Group 2008-11-05 2008-10-16 /pmc/articles/PMC2570475/ /pubmed/18923420 http://dx.doi.org/10.1038/emboj.2008.217 Text en Copyright © 2008, European Molecular Biology Organization http://creativecommons.org/licenses/by-nc-nd/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits distribution, and reproduction in any medium, provided the original author and source are credited. This licence does not permit commercial exploitation or the creation of derivative works without specific permission.
spellingShingle New EMBO Member's Review
Nilius, Bernd
Owsianik, Grzegorz
Voets, Thomas
Transient receptor potential channels meet phosphoinositides
title Transient receptor potential channels meet phosphoinositides
title_full Transient receptor potential channels meet phosphoinositides
title_fullStr Transient receptor potential channels meet phosphoinositides
title_full_unstemmed Transient receptor potential channels meet phosphoinositides
title_short Transient receptor potential channels meet phosphoinositides
title_sort transient receptor potential channels meet phosphoinositides
topic New EMBO Member's Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2570475/
https://www.ncbi.nlm.nih.gov/pubmed/18923420
http://dx.doi.org/10.1038/emboj.2008.217
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