Src inhibition attenuates polyglutamine-mediated neuromuscular degeneration in spinal and bulbar muscular atrophy

Spinal and bulbar muscular atrophy is a neuromuscular disease caused by an expanded CAG repeat in the androgen receptor gene. Here the authors show that Src kinase signaling is activated in a mouse model of the disease, and that Src inhibition improves pathology and behavioral symptoms in mice.

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Autores principales: Madoka Iida, Kentaro Sahashi, Naohide Kondo, Hideaki Nakatsuji, Genki Tohnai, Yutaka Tsutsumi, Seiya Noda, Ayuka Murakami, Kazunari Onodera, Yohei Okada, Masahiro Nakatochi, Yuka Tsukagoshi Okabe, Shinobu Shimizu, Masaaki Mizuno, Hiroaki Adachi, Hideyuki Okano, Gen Sobue, Masahisa Katsuno
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Lenguaje:EN
Publicado: Nature Portfolio 2019
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Acceso en línea:https://doaj.org/article/847b1385413f4d0583de48824f421c0e
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spelling oai:doaj.org-article:847b1385413f4d0583de48824f421c0e2021-12-02T15:35:29ZSrc inhibition attenuates polyglutamine-mediated neuromuscular degeneration in spinal and bulbar muscular atrophy10.1038/s41467-019-12282-72041-1723https://doaj.org/article/847b1385413f4d0583de48824f421c0e2019-09-01T00:00:00Zhttps://doi.org/10.1038/s41467-019-12282-7https://doaj.org/toc/2041-1723Spinal and bulbar muscular atrophy is a neuromuscular disease caused by an expanded CAG repeat in the androgen receptor gene. Here the authors show that Src kinase signaling is activated in a mouse model of the disease, and that Src inhibition improves pathology and behavioral symptoms in mice.Madoka IidaKentaro SahashiNaohide KondoHideaki NakatsujiGenki TohnaiYutaka TsutsumiSeiya NodaAyuka MurakamiKazunari OnoderaYohei OkadaMasahiro NakatochiYuka Tsukagoshi OkabeShinobu ShimizuMasaaki MizunoHiroaki AdachiHideyuki OkanoGen SobueMasahisa KatsunoNature PortfolioarticleScienceQENNature Communications, Vol 10, Iss 1, Pp 1-15 (2019)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Madoka Iida
Kentaro Sahashi
Naohide Kondo
Hideaki Nakatsuji
Genki Tohnai
Yutaka Tsutsumi
Seiya Noda
Ayuka Murakami
Kazunari Onodera
Yohei Okada
Masahiro Nakatochi
Yuka Tsukagoshi Okabe
Shinobu Shimizu
Masaaki Mizuno
Hiroaki Adachi
Hideyuki Okano
Gen Sobue
Masahisa Katsuno
Src inhibition attenuates polyglutamine-mediated neuromuscular degeneration in spinal and bulbar muscular atrophy
description Spinal and bulbar muscular atrophy is a neuromuscular disease caused by an expanded CAG repeat in the androgen receptor gene. Here the authors show that Src kinase signaling is activated in a mouse model of the disease, and that Src inhibition improves pathology and behavioral symptoms in mice.
format article
author Madoka Iida
Kentaro Sahashi
Naohide Kondo
Hideaki Nakatsuji
Genki Tohnai
Yutaka Tsutsumi
Seiya Noda
Ayuka Murakami
Kazunari Onodera
Yohei Okada
Masahiro Nakatochi
Yuka Tsukagoshi Okabe
Shinobu Shimizu
Masaaki Mizuno
Hiroaki Adachi
Hideyuki Okano
Gen Sobue
Masahisa Katsuno
author_facet Madoka Iida
Kentaro Sahashi
Naohide Kondo
Hideaki Nakatsuji
Genki Tohnai
Yutaka Tsutsumi
Seiya Noda
Ayuka Murakami
Kazunari Onodera
Yohei Okada
Masahiro Nakatochi
Yuka Tsukagoshi Okabe
Shinobu Shimizu
Masaaki Mizuno
Hiroaki Adachi
Hideyuki Okano
Gen Sobue
Masahisa Katsuno
author_sort Madoka Iida
title Src inhibition attenuates polyglutamine-mediated neuromuscular degeneration in spinal and bulbar muscular atrophy
title_short Src inhibition attenuates polyglutamine-mediated neuromuscular degeneration in spinal and bulbar muscular atrophy
title_full Src inhibition attenuates polyglutamine-mediated neuromuscular degeneration in spinal and bulbar muscular atrophy
title_fullStr Src inhibition attenuates polyglutamine-mediated neuromuscular degeneration in spinal and bulbar muscular atrophy
title_full_unstemmed Src inhibition attenuates polyglutamine-mediated neuromuscular degeneration in spinal and bulbar muscular atrophy
title_sort src inhibition attenuates polyglutamine-mediated neuromuscular degeneration in spinal and bulbar muscular atrophy
publisher Nature Portfolio
publishDate 2019
url https://doaj.org/article/847b1385413f4d0583de48824f421c0e
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