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Natural and Synthetic Modulators of the TRPM7 Channel

Transient receptor potential cation channel subfamily M member 7 (TRPM7) is a bi-functional protein comprising a TRP ion channel segment linked to an α-type protein kinase domain. Genetic inactivation of TRPM7 revealed its central role in magnesium metabolism, cell motility, proliferation and differ...

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Detalles Bibliográficos
Autores principales: Chubanov, Vladimir, Schäfer, Sebastian, Ferioli, Silvia, Gudermann, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4276914/
https://www.ncbi.nlm.nih.gov/pubmed/25437439
http://dx.doi.org/10.3390/cells3041089
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author Chubanov, Vladimir
Schäfer, Sebastian
Ferioli, Silvia
Gudermann, Thomas
author_facet Chubanov, Vladimir
Schäfer, Sebastian
Ferioli, Silvia
Gudermann, Thomas
author_sort Chubanov, Vladimir
collection PubMed
description Transient receptor potential cation channel subfamily M member 7 (TRPM7) is a bi-functional protein comprising a TRP ion channel segment linked to an α-type protein kinase domain. Genetic inactivation of TRPM7 revealed its central role in magnesium metabolism, cell motility, proliferation and differentiation. TRPM7 is associated with anoxic neuronal death, cardiac fibrosis and tumor progression highlighting TRPM7 as a new drug target. Recently, several laboratories have independently identified pharmacological compounds inhibiting or activating the TRPM7 channel. The recently found TRPM7 modulators were used as new experimental tools to unravel cellular functions of the TRPM7 channel. Here, we provide a concise overview of this emerging field.
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spelling pubmed-42769142015-01-15 Natural and Synthetic Modulators of the TRPM7 Channel Chubanov, Vladimir Schäfer, Sebastian Ferioli, Silvia Gudermann, Thomas Cells Review Transient receptor potential cation channel subfamily M member 7 (TRPM7) is a bi-functional protein comprising a TRP ion channel segment linked to an α-type protein kinase domain. Genetic inactivation of TRPM7 revealed its central role in magnesium metabolism, cell motility, proliferation and differentiation. TRPM7 is associated with anoxic neuronal death, cardiac fibrosis and tumor progression highlighting TRPM7 as a new drug target. Recently, several laboratories have independently identified pharmacological compounds inhibiting or activating the TRPM7 channel. The recently found TRPM7 modulators were used as new experimental tools to unravel cellular functions of the TRPM7 channel. Here, we provide a concise overview of this emerging field. MDPI 2014-11-27 /pmc/articles/PMC4276914/ /pubmed/25437439 http://dx.doi.org/10.3390/cells3041089 Text en © 2014 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Chubanov, Vladimir
Schäfer, Sebastian
Ferioli, Silvia
Gudermann, Thomas
Natural and Synthetic Modulators of the TRPM7 Channel
title Natural and Synthetic Modulators of the TRPM7 Channel
title_full Natural and Synthetic Modulators of the TRPM7 Channel
title_fullStr Natural and Synthetic Modulators of the TRPM7 Channel
title_full_unstemmed Natural and Synthetic Modulators of the TRPM7 Channel
title_short Natural and Synthetic Modulators of the TRPM7 Channel
title_sort natural and synthetic modulators of the trpm7 channel
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4276914/
https://www.ncbi.nlm.nih.gov/pubmed/25437439
http://dx.doi.org/10.3390/cells3041089
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