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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,...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2008
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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. |
format | Text |
id | pubmed-2621155 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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