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Heparan Sulfates Regulate Axonal Excitability and Context Generalization through Ca(2+)/Calmodulin-Dependent Protein Kinase II

Our previous studies demonstrated that enzymatic removal of highly sulfated heparan sulfates with heparinase 1 impaired axonal excitability and reduced expression of ankyrin G at the axon initial segments in the CA1 region of the hippocampus ex vivo, impaired context discrimination in vivo, and incr...

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Autores principales: Song, Inseon, Kuznetsova, Tatiana, Baidoe-Ansah, David, Mirzapourdelavar, Hadi, Senkov, Oleg, Hayani, Hussam, Mironov, Andrey, Kaushik, Rahul, Druzin, Michael, Johansson, Staffan, Dityatev, Alexander
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10000602/
https://www.ncbi.nlm.nih.gov/pubmed/36899880
http://dx.doi.org/10.3390/cells12050744
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author Song, Inseon
Kuznetsova, Tatiana
Baidoe-Ansah, David
Mirzapourdelavar, Hadi
Senkov, Oleg
Hayani, Hussam
Mironov, Andrey
Kaushik, Rahul
Druzin, Michael
Johansson, Staffan
Dityatev, Alexander
author_facet Song, Inseon
Kuznetsova, Tatiana
Baidoe-Ansah, David
Mirzapourdelavar, Hadi
Senkov, Oleg
Hayani, Hussam
Mironov, Andrey
Kaushik, Rahul
Druzin, Michael
Johansson, Staffan
Dityatev, Alexander
author_sort Song, Inseon
collection PubMed
description Our previous studies demonstrated that enzymatic removal of highly sulfated heparan sulfates with heparinase 1 impaired axonal excitability and reduced expression of ankyrin G at the axon initial segments in the CA1 region of the hippocampus ex vivo, impaired context discrimination in vivo, and increased Ca(2+)/calmodulin-dependent protein kinase II (CaMKII) activity in vitro. Here, we show that in vivo delivery of heparinase 1 in the CA1 region of the hippocampus elevated autophosphorylation of CaMKII 24 h after injection in mice. Patch clamp recording in CA1 neurons revealed no significant heparinase effects on the amplitude or frequency of miniature excitatory and inhibitory postsynaptic currents, while the threshold for action potential generation was increased and fewer spikes were generated in response to current injection. Delivery of heparinase on the next day after contextual fear conditioning induced context overgeneralization 24 h after injection. Co-administration of heparinase with the CaMKII inhibitor (autocamtide-2-related inhibitory peptide) rescued neuronal excitability and expression of ankyrin G at the axon initial segment. It also restored context discrimination, suggesting the key role of CaMKII in neuronal signaling downstream of heparan sulfate proteoglycans and highlighting a link between impaired CA1 pyramidal cell excitability and context generalization during recall of contextual memories.
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spelling pubmed-100006022023-03-11 Heparan Sulfates Regulate Axonal Excitability and Context Generalization through Ca(2+)/Calmodulin-Dependent Protein Kinase II Song, Inseon Kuznetsova, Tatiana Baidoe-Ansah, David Mirzapourdelavar, Hadi Senkov, Oleg Hayani, Hussam Mironov, Andrey Kaushik, Rahul Druzin, Michael Johansson, Staffan Dityatev, Alexander Cells Article Our previous studies demonstrated that enzymatic removal of highly sulfated heparan sulfates with heparinase 1 impaired axonal excitability and reduced expression of ankyrin G at the axon initial segments in the CA1 region of the hippocampus ex vivo, impaired context discrimination in vivo, and increased Ca(2+)/calmodulin-dependent protein kinase II (CaMKII) activity in vitro. Here, we show that in vivo delivery of heparinase 1 in the CA1 region of the hippocampus elevated autophosphorylation of CaMKII 24 h after injection in mice. Patch clamp recording in CA1 neurons revealed no significant heparinase effects on the amplitude or frequency of miniature excitatory and inhibitory postsynaptic currents, while the threshold for action potential generation was increased and fewer spikes were generated in response to current injection. Delivery of heparinase on the next day after contextual fear conditioning induced context overgeneralization 24 h after injection. Co-administration of heparinase with the CaMKII inhibitor (autocamtide-2-related inhibitory peptide) rescued neuronal excitability and expression of ankyrin G at the axon initial segment. It also restored context discrimination, suggesting the key role of CaMKII in neuronal signaling downstream of heparan sulfate proteoglycans and highlighting a link between impaired CA1 pyramidal cell excitability and context generalization during recall of contextual memories. MDPI 2023-02-25 /pmc/articles/PMC10000602/ /pubmed/36899880 http://dx.doi.org/10.3390/cells12050744 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Song, Inseon
Kuznetsova, Tatiana
Baidoe-Ansah, David
Mirzapourdelavar, Hadi
Senkov, Oleg
Hayani, Hussam
Mironov, Andrey
Kaushik, Rahul
Druzin, Michael
Johansson, Staffan
Dityatev, Alexander
Heparan Sulfates Regulate Axonal Excitability and Context Generalization through Ca(2+)/Calmodulin-Dependent Protein Kinase II
title Heparan Sulfates Regulate Axonal Excitability and Context Generalization through Ca(2+)/Calmodulin-Dependent Protein Kinase II
title_full Heparan Sulfates Regulate Axonal Excitability and Context Generalization through Ca(2+)/Calmodulin-Dependent Protein Kinase II
title_fullStr Heparan Sulfates Regulate Axonal Excitability and Context Generalization through Ca(2+)/Calmodulin-Dependent Protein Kinase II
title_full_unstemmed Heparan Sulfates Regulate Axonal Excitability and Context Generalization through Ca(2+)/Calmodulin-Dependent Protein Kinase II
title_short Heparan Sulfates Regulate Axonal Excitability and Context Generalization through Ca(2+)/Calmodulin-Dependent Protein Kinase II
title_sort heparan sulfates regulate axonal excitability and context generalization through ca(2+)/calmodulin-dependent protein kinase ii
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10000602/
https://www.ncbi.nlm.nih.gov/pubmed/36899880
http://dx.doi.org/10.3390/cells12050744
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