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alpha-Actinin interacts with rapsyn in agrin-stimulated AChR clustering

AChR is concentrated at the postjunctional membrane at the neuromuscular junction. However, the underlying mechanism is unclear. We show that α-actinin, a protein known to cross-link F-actin, interacts with rapsyn, a scaffold protein essential for neuromuscular junction formation. α-Actinin, rapsyn,...

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Detalles Bibliográficos
Autores principales: Dobbins, G Clement, Luo, Shiwen, Yang, Zhihua, Xiong, Wen C, Mei, Lin
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2621155/
https://www.ncbi.nlm.nih.gov/pubmed/19055765
http://dx.doi.org/10.1186/1756-6606-1-18
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author Dobbins, G Clement
Luo, Shiwen
Yang, Zhihua
Xiong, Wen C
Mei, Lin
author_facet Dobbins, G Clement
Luo, Shiwen
Yang, Zhihua
Xiong, Wen C
Mei, Lin
author_sort Dobbins, G Clement
collection PubMed
description AChR is concentrated at the postjunctional membrane at the neuromuscular junction. However, the underlying mechanism is unclear. We show that α-actinin, a protein known to cross-link F-actin, interacts with rapsyn, a scaffold protein essential for neuromuscular junction formation. α-Actinin, rapsyn, and surface AChR form a ternary complex. Moreover, the rapsyn-α-actinin interaction is increased by agrin, a factor known to stimulate AChR clustering. Downregulation of α-actinin expression inhibits agrin-mediated AChR clustering. Furthermore, the rapsyn-α-actinin interaction can be disrupted by inhibiting Abl and by cholinergic stimulation. Together these results indicate a role for α-actinin in AChR clustering.
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spelling pubmed-26211552009-01-13 alpha-Actinin interacts with rapsyn in agrin-stimulated AChR clustering Dobbins, G Clement Luo, Shiwen Yang, Zhihua Xiong, Wen C Mei, Lin Mol Brain Research AChR is concentrated at the postjunctional membrane at the neuromuscular junction. However, the underlying mechanism is unclear. We show that α-actinin, a protein known to cross-link F-actin, interacts with rapsyn, a scaffold protein essential for neuromuscular junction formation. α-Actinin, rapsyn, and surface AChR form a ternary complex. Moreover, the rapsyn-α-actinin interaction is increased by agrin, a factor known to stimulate AChR clustering. Downregulation of α-actinin expression inhibits agrin-mediated AChR clustering. Furthermore, the rapsyn-α-actinin interaction can be disrupted by inhibiting Abl and by cholinergic stimulation. Together these results indicate a role for α-actinin in AChR clustering. BioMed Central 2008-12-03 /pmc/articles/PMC2621155/ /pubmed/19055765 http://dx.doi.org/10.1186/1756-6606-1-18 Text en Copyright © 2008 Dobbins et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Dobbins, G Clement
Luo, Shiwen
Yang, Zhihua
Xiong, Wen C
Mei, Lin
alpha-Actinin interacts with rapsyn in agrin-stimulated AChR clustering
title alpha-Actinin interacts with rapsyn in agrin-stimulated AChR clustering
title_full alpha-Actinin interacts with rapsyn in agrin-stimulated AChR clustering
title_fullStr alpha-Actinin interacts with rapsyn in agrin-stimulated AChR clustering
title_full_unstemmed alpha-Actinin interacts with rapsyn in agrin-stimulated AChR clustering
title_short alpha-Actinin interacts with rapsyn in agrin-stimulated AChR clustering
title_sort alpha-actinin interacts with rapsyn in agrin-stimulated achr clustering
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2621155/
https://www.ncbi.nlm.nih.gov/pubmed/19055765
http://dx.doi.org/10.1186/1756-6606-1-18
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