Neuropathy-causing TRPV4 mutations disrupt TRPV4-RhoA interactions and impair neurite extension

TRPV4 dominant mutations cause neuropathy. Here, the authors show that TRPV4 binds and interacts with RhoA, modulating the actin cytoskeleton. Neuropathy-causing mutations of TRPV4 disrupt this complex, leading to RhoA activation and impairment of neurite extension in cultured cells and flies.

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Autores principales: Brett A. McCray, Erika Diehl, Jeremy M. Sullivan, William H. Aisenberg, Nicholas W. Zaccor, Alexander R. Lau, Dominick J. Rich, Benedikt Goretzki, Ute A. Hellmich, Thomas E. Lloyd, Charlotte J. Sumner
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Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/c12c32fb25af4c0fbec8907050b017a1
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spelling oai:doaj.org-article:c12c32fb25af4c0fbec8907050b017a12021-12-02T13:33:01ZNeuropathy-causing TRPV4 mutations disrupt TRPV4-RhoA interactions and impair neurite extension10.1038/s41467-021-21699-y2041-1723https://doaj.org/article/c12c32fb25af4c0fbec8907050b017a12021-03-01T00:00:00Zhttps://doi.org/10.1038/s41467-021-21699-yhttps://doaj.org/toc/2041-1723TRPV4 dominant mutations cause neuropathy. Here, the authors show that TRPV4 binds and interacts with RhoA, modulating the actin cytoskeleton. Neuropathy-causing mutations of TRPV4 disrupt this complex, leading to RhoA activation and impairment of neurite extension in cultured cells and flies.Brett A. McCrayErika DiehlJeremy M. SullivanWilliam H. AisenbergNicholas W. ZaccorAlexander R. LauDominick J. RichBenedikt GoretzkiUte A. HellmichThomas E. LloydCharlotte J. SumnerNature PortfolioarticleScienceQENNature Communications, Vol 12, Iss 1, Pp 1-17 (2021)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Brett A. McCray
Erika Diehl
Jeremy M. Sullivan
William H. Aisenberg
Nicholas W. Zaccor
Alexander R. Lau
Dominick J. Rich
Benedikt Goretzki
Ute A. Hellmich
Thomas E. Lloyd
Charlotte J. Sumner
Neuropathy-causing TRPV4 mutations disrupt TRPV4-RhoA interactions and impair neurite extension
description TRPV4 dominant mutations cause neuropathy. Here, the authors show that TRPV4 binds and interacts with RhoA, modulating the actin cytoskeleton. Neuropathy-causing mutations of TRPV4 disrupt this complex, leading to RhoA activation and impairment of neurite extension in cultured cells and flies.
format article
author Brett A. McCray
Erika Diehl
Jeremy M. Sullivan
William H. Aisenberg
Nicholas W. Zaccor
Alexander R. Lau
Dominick J. Rich
Benedikt Goretzki
Ute A. Hellmich
Thomas E. Lloyd
Charlotte J. Sumner
author_facet Brett A. McCray
Erika Diehl
Jeremy M. Sullivan
William H. Aisenberg
Nicholas W. Zaccor
Alexander R. Lau
Dominick J. Rich
Benedikt Goretzki
Ute A. Hellmich
Thomas E. Lloyd
Charlotte J. Sumner
author_sort Brett A. McCray
title Neuropathy-causing TRPV4 mutations disrupt TRPV4-RhoA interactions and impair neurite extension
title_short Neuropathy-causing TRPV4 mutations disrupt TRPV4-RhoA interactions and impair neurite extension
title_full Neuropathy-causing TRPV4 mutations disrupt TRPV4-RhoA interactions and impair neurite extension
title_fullStr Neuropathy-causing TRPV4 mutations disrupt TRPV4-RhoA interactions and impair neurite extension
title_full_unstemmed Neuropathy-causing TRPV4 mutations disrupt TRPV4-RhoA interactions and impair neurite extension
title_sort neuropathy-causing trpv4 mutations disrupt trpv4-rhoa interactions and impair neurite extension
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/c12c32fb25af4c0fbec8907050b017a1
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