Cargando…

The C-terminus SH3-binding domain of Kv1.3 is required for the actin-mediated immobilization of the channel via cortactin

Kv1.3 channels play a pivotal role in the activation and migration of T-lymphocytes. These functions are accompanied by the channels' polarization, which is essential for associated downstream events. However, the mechanisms that govern the membrane movement of Kv1.3 channels remain unclear. F-...

Descripción completa

Detalles Bibliográficos
Autores principales: Hajdu, Peter, Martin, Geoffrey V., Chimote, Ameet A., Szilagyi, Orsolya, Takimoto, Koichi, Conforti, Laura
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Cell Biology 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4436776/
https://www.ncbi.nlm.nih.gov/pubmed/25739456
http://dx.doi.org/10.1091/mbc.E14-07-1195
_version_ 1782372128123781120
author Hajdu, Peter
Martin, Geoffrey V.
Chimote, Ameet A.
Szilagyi, Orsolya
Takimoto, Koichi
Conforti, Laura
author_facet Hajdu, Peter
Martin, Geoffrey V.
Chimote, Ameet A.
Szilagyi, Orsolya
Takimoto, Koichi
Conforti, Laura
author_sort Hajdu, Peter
collection PubMed
description Kv1.3 channels play a pivotal role in the activation and migration of T-lymphocytes. These functions are accompanied by the channels' polarization, which is essential for associated downstream events. However, the mechanisms that govern the membrane movement of Kv1.3 channels remain unclear. F-actin polymerization occurs concomitantly to channel polarization, implicating the actin cytoskeleton in this process. Here we show that cortactin, a factor initiating the actin network, controls the membrane mobilization of Kv1.3 channels. FRAP with EGFP-tagged Kv1.3 channels demonstrates that knocking down cortactin decreases the actin-based immobilization of the channels. Using various deletion and mutation constructs, we show that the SH3 motif of Kv1.3 mediates the channel immobilization. Proximity ligation assays indicate that deletion or mutation of the SH3 motif also disrupts interaction of the channel with cortactin. In T-lymphocytes, the interaction between HS1 (the cortactin homologue) and Kv1.3 occurs at the immune synapse and requires the channel's C-terminal domain. These results show that actin dynamics regulates the membrane motility of Kv1.3 channels. They also provide evidence that the SH3 motif of the channel and cortactin plays key roles in this process.
format Online
Article
Text
id pubmed-4436776
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher The American Society for Cell Biology
record_format MEDLINE/PubMed
spelling pubmed-44367762015-07-16 The C-terminus SH3-binding domain of Kv1.3 is required for the actin-mediated immobilization of the channel via cortactin Hajdu, Peter Martin, Geoffrey V. Chimote, Ameet A. Szilagyi, Orsolya Takimoto, Koichi Conforti, Laura Mol Biol Cell Articles Kv1.3 channels play a pivotal role in the activation and migration of T-lymphocytes. These functions are accompanied by the channels' polarization, which is essential for associated downstream events. However, the mechanisms that govern the membrane movement of Kv1.3 channels remain unclear. F-actin polymerization occurs concomitantly to channel polarization, implicating the actin cytoskeleton in this process. Here we show that cortactin, a factor initiating the actin network, controls the membrane mobilization of Kv1.3 channels. FRAP with EGFP-tagged Kv1.3 channels demonstrates that knocking down cortactin decreases the actin-based immobilization of the channels. Using various deletion and mutation constructs, we show that the SH3 motif of Kv1.3 mediates the channel immobilization. Proximity ligation assays indicate that deletion or mutation of the SH3 motif also disrupts interaction of the channel with cortactin. In T-lymphocytes, the interaction between HS1 (the cortactin homologue) and Kv1.3 occurs at the immune synapse and requires the channel's C-terminal domain. These results show that actin dynamics regulates the membrane motility of Kv1.3 channels. They also provide evidence that the SH3 motif of the channel and cortactin plays key roles in this process. The American Society for Cell Biology 2015-05-01 /pmc/articles/PMC4436776/ /pubmed/25739456 http://dx.doi.org/10.1091/mbc.E14-07-1195 Text en © 2015 Hajdu et al. This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License (http://creativecommons.org/licenses/by-nc-sa/3.0). “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology.
spellingShingle Articles
Hajdu, Peter
Martin, Geoffrey V.
Chimote, Ameet A.
Szilagyi, Orsolya
Takimoto, Koichi
Conforti, Laura
The C-terminus SH3-binding domain of Kv1.3 is required for the actin-mediated immobilization of the channel via cortactin
title The C-terminus SH3-binding domain of Kv1.3 is required for the actin-mediated immobilization of the channel via cortactin
title_full The C-terminus SH3-binding domain of Kv1.3 is required for the actin-mediated immobilization of the channel via cortactin
title_fullStr The C-terminus SH3-binding domain of Kv1.3 is required for the actin-mediated immobilization of the channel via cortactin
title_full_unstemmed The C-terminus SH3-binding domain of Kv1.3 is required for the actin-mediated immobilization of the channel via cortactin
title_short The C-terminus SH3-binding domain of Kv1.3 is required for the actin-mediated immobilization of the channel via cortactin
title_sort c-terminus sh3-binding domain of kv1.3 is required for the actin-mediated immobilization of the channel via cortactin
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4436776/
https://www.ncbi.nlm.nih.gov/pubmed/25739456
http://dx.doi.org/10.1091/mbc.E14-07-1195
work_keys_str_mv AT hajdupeter thecterminussh3bindingdomainofkv13isrequiredfortheactinmediatedimmobilizationofthechannelviacortactin
AT martingeoffreyv thecterminussh3bindingdomainofkv13isrequiredfortheactinmediatedimmobilizationofthechannelviacortactin
AT chimoteameeta thecterminussh3bindingdomainofkv13isrequiredfortheactinmediatedimmobilizationofthechannelviacortactin
AT szilagyiorsolya thecterminussh3bindingdomainofkv13isrequiredfortheactinmediatedimmobilizationofthechannelviacortactin
AT takimotokoichi thecterminussh3bindingdomainofkv13isrequiredfortheactinmediatedimmobilizationofthechannelviacortactin
AT confortilaura thecterminussh3bindingdomainofkv13isrequiredfortheactinmediatedimmobilizationofthechannelviacortactin
AT hajdupeter cterminussh3bindingdomainofkv13isrequiredfortheactinmediatedimmobilizationofthechannelviacortactin
AT martingeoffreyv cterminussh3bindingdomainofkv13isrequiredfortheactinmediatedimmobilizationofthechannelviacortactin
AT chimoteameeta cterminussh3bindingdomainofkv13isrequiredfortheactinmediatedimmobilizationofthechannelviacortactin
AT szilagyiorsolya cterminussh3bindingdomainofkv13isrequiredfortheactinmediatedimmobilizationofthechannelviacortactin
AT takimotokoichi cterminussh3bindingdomainofkv13isrequiredfortheactinmediatedimmobilizationofthechannelviacortactin
AT confortilaura cterminussh3bindingdomainofkv13isrequiredfortheactinmediatedimmobilizationofthechannelviacortactin