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The p75 receptor transduces the signal from myelin-associated glycoprotein to Rho

Myelin-associated glycoprotein (MAG) is a potent inhibitor of neurite outgrowth from a variety of neurons. The receptor for MAG or signals that elicit morphological changes in neurons remained to be established. Here we show that the neurotrophin receptor p75 (p75(NTR)) is the signal transducing ele...

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Detalles Bibliográficos
Autores principales: Yamashita, Toshihide, Higuchi, Haruhisa, Tohyama, Masaya
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2002
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2173856/
https://www.ncbi.nlm.nih.gov/pubmed/12011108
http://dx.doi.org/10.1083/jcb.200202010
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author Yamashita, Toshihide
Higuchi, Haruhisa
Tohyama, Masaya
author_facet Yamashita, Toshihide
Higuchi, Haruhisa
Tohyama, Masaya
author_sort Yamashita, Toshihide
collection PubMed
description Myelin-associated glycoprotein (MAG) is a potent inhibitor of neurite outgrowth from a variety of neurons. The receptor for MAG or signals that elicit morphological changes in neurons remained to be established. Here we show that the neurotrophin receptor p75 (p75(NTR)) is the signal transducing element for MAG. Adult dorsal root ganglion neurons or postnatal cerebellar neurons from mice carrying a mutation in the p75(NTR) gene are insensitive to MAG with regard to neurite outgrowth. MAG activates small GTPase RhoA, leading to retarded outgrowth when p75(NTR) is present. Colocalization of p75(NTR) and MAG binding is seen in neurons. Ganglioside GT1b, which is one of the binding partners of MAG, specifically associates with p75(NTR). Thus, p75(NTR) and GT1b may form a receptor complex for MAG to transmit the inhibitory signals in neurons.
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spelling pubmed-21738562008-05-01 The p75 receptor transduces the signal from myelin-associated glycoprotein to Rho Yamashita, Toshihide Higuchi, Haruhisa Tohyama, Masaya J Cell Biol Report Myelin-associated glycoprotein (MAG) is a potent inhibitor of neurite outgrowth from a variety of neurons. The receptor for MAG or signals that elicit morphological changes in neurons remained to be established. Here we show that the neurotrophin receptor p75 (p75(NTR)) is the signal transducing element for MAG. Adult dorsal root ganglion neurons or postnatal cerebellar neurons from mice carrying a mutation in the p75(NTR) gene are insensitive to MAG with regard to neurite outgrowth. MAG activates small GTPase RhoA, leading to retarded outgrowth when p75(NTR) is present. Colocalization of p75(NTR) and MAG binding is seen in neurons. Ganglioside GT1b, which is one of the binding partners of MAG, specifically associates with p75(NTR). Thus, p75(NTR) and GT1b may form a receptor complex for MAG to transmit the inhibitory signals in neurons. The Rockefeller University Press 2002-05-13 /pmc/articles/PMC2173856/ /pubmed/12011108 http://dx.doi.org/10.1083/jcb.200202010 Text en Copyright © 2002, The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Report
Yamashita, Toshihide
Higuchi, Haruhisa
Tohyama, Masaya
The p75 receptor transduces the signal from myelin-associated glycoprotein to Rho
title The p75 receptor transduces the signal from myelin-associated glycoprotein to Rho
title_full The p75 receptor transduces the signal from myelin-associated glycoprotein to Rho
title_fullStr The p75 receptor transduces the signal from myelin-associated glycoprotein to Rho
title_full_unstemmed The p75 receptor transduces the signal from myelin-associated glycoprotein to Rho
title_short The p75 receptor transduces the signal from myelin-associated glycoprotein to Rho
title_sort p75 receptor transduces the signal from myelin-associated glycoprotein to rho
topic Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2173856/
https://www.ncbi.nlm.nih.gov/pubmed/12011108
http://dx.doi.org/10.1083/jcb.200202010
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