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C-Terminal Interactors of the AMPA Receptor Auxiliary Subunit Shisa9

Shisa9 (initially named CKAMP44) has been identified as auxiliary subunit of the AMPA-type glutamate receptors and was shown to modulate its physiological properties. Shisa9 is a type-I transmembrane protein and contains a C-terminal PDZ domain that potentially interacts with cytosolic proteins. In...

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Autores principales: Karataeva, Anna R., Klaassen, Remco V., Ströder, Jasper, Ruiperez-Alonso, Marta, Hjorth, Johannes J. J., van Nierop, Pim, Spijker, Sabine, Mansvelder, Huibert D., Smit, August B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3911953/
https://www.ncbi.nlm.nih.gov/pubmed/24498314
http://dx.doi.org/10.1371/journal.pone.0087360
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author Karataeva, Anna R.
Klaassen, Remco V.
Ströder, Jasper
Ruiperez-Alonso, Marta
Hjorth, Johannes J. J.
van Nierop, Pim
Spijker, Sabine
Mansvelder, Huibert D.
Smit, August B.
author_facet Karataeva, Anna R.
Klaassen, Remco V.
Ströder, Jasper
Ruiperez-Alonso, Marta
Hjorth, Johannes J. J.
van Nierop, Pim
Spijker, Sabine
Mansvelder, Huibert D.
Smit, August B.
author_sort Karataeva, Anna R.
collection PubMed
description Shisa9 (initially named CKAMP44) has been identified as auxiliary subunit of the AMPA-type glutamate receptors and was shown to modulate its physiological properties. Shisa9 is a type-I transmembrane protein and contains a C-terminal PDZ domain that potentially interacts with cytosolic proteins. In this study, we performed a yeast two-hybrid screening that yielded eight PDZ domain-containing interactors of Shisa9, which were independently validated. The identified interactors are known scaffolding proteins residing in the neuronal postsynaptic density. To test whether C-terminal scaffolding interactions of Shisa9 affect synaptic AMPA receptor function in the hippocampus, we disrupted these interactions using a Shisa9 C-terminal mimetic peptide. In the absence of scaffolding interactions of Shisa9, glutamatergic AMPA receptor-mediated synaptic currents in the lateral perforant path of the mouse hippocampus had a faster decay time, and paired-pulse facilitation was reduced. Furthermore, disruption of the PDZ interactions between Shisa9 and its binding partners affected hippocampal network activity. Taken together, our data identifies novel interaction partners of Shisa9, and shows that the C-terminal interactions of Shisa9 through its PDZ domain interaction motif are important for AMPA receptor synaptic and network functions.
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spelling pubmed-39119532014-02-04 C-Terminal Interactors of the AMPA Receptor Auxiliary Subunit Shisa9 Karataeva, Anna R. Klaassen, Remco V. Ströder, Jasper Ruiperez-Alonso, Marta Hjorth, Johannes J. J. van Nierop, Pim Spijker, Sabine Mansvelder, Huibert D. Smit, August B. PLoS One Research Article Shisa9 (initially named CKAMP44) has been identified as auxiliary subunit of the AMPA-type glutamate receptors and was shown to modulate its physiological properties. Shisa9 is a type-I transmembrane protein and contains a C-terminal PDZ domain that potentially interacts with cytosolic proteins. In this study, we performed a yeast two-hybrid screening that yielded eight PDZ domain-containing interactors of Shisa9, which were independently validated. The identified interactors are known scaffolding proteins residing in the neuronal postsynaptic density. To test whether C-terminal scaffolding interactions of Shisa9 affect synaptic AMPA receptor function in the hippocampus, we disrupted these interactions using a Shisa9 C-terminal mimetic peptide. In the absence of scaffolding interactions of Shisa9, glutamatergic AMPA receptor-mediated synaptic currents in the lateral perforant path of the mouse hippocampus had a faster decay time, and paired-pulse facilitation was reduced. Furthermore, disruption of the PDZ interactions between Shisa9 and its binding partners affected hippocampal network activity. Taken together, our data identifies novel interaction partners of Shisa9, and shows that the C-terminal interactions of Shisa9 through its PDZ domain interaction motif are important for AMPA receptor synaptic and network functions. Public Library of Science 2014-02-03 /pmc/articles/PMC3911953/ /pubmed/24498314 http://dx.doi.org/10.1371/journal.pone.0087360 Text en © 2014 Karataeva et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Karataeva, Anna R.
Klaassen, Remco V.
Ströder, Jasper
Ruiperez-Alonso, Marta
Hjorth, Johannes J. J.
van Nierop, Pim
Spijker, Sabine
Mansvelder, Huibert D.
Smit, August B.
C-Terminal Interactors of the AMPA Receptor Auxiliary Subunit Shisa9
title C-Terminal Interactors of the AMPA Receptor Auxiliary Subunit Shisa9
title_full C-Terminal Interactors of the AMPA Receptor Auxiliary Subunit Shisa9
title_fullStr C-Terminal Interactors of the AMPA Receptor Auxiliary Subunit Shisa9
title_full_unstemmed C-Terminal Interactors of the AMPA Receptor Auxiliary Subunit Shisa9
title_short C-Terminal Interactors of the AMPA Receptor Auxiliary Subunit Shisa9
title_sort c-terminal interactors of the ampa receptor auxiliary subunit shisa9
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3911953/
https://www.ncbi.nlm.nih.gov/pubmed/24498314
http://dx.doi.org/10.1371/journal.pone.0087360
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