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Targeted deletion of AKAP7 in dentate granule cells impairs spatial discrimination
Protein Kinase A (PKA) mediates synaptic plasticity and is widely implicated in learning and memory. The hippocampal dentate gyrus (DG) is thought to be responsible for processing and encoding distinct contextual associations in response to highly similar inputs. The mossy fiber (MF) axons of the de...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5135391/ https://www.ncbi.nlm.nih.gov/pubmed/27911261 http://dx.doi.org/10.7554/eLife.20695 |
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author | Jones, Brian W Deem, Jennifer Younts, Thomas J Weisenhaus, Michael Sanford, Christina A Slack, Margaret C Chin, Jenesa Nachmanson, Daniela McKennon, Alex Castillo, Pablo E McKnight, G Stanley |
author_facet | Jones, Brian W Deem, Jennifer Younts, Thomas J Weisenhaus, Michael Sanford, Christina A Slack, Margaret C Chin, Jenesa Nachmanson, Daniela McKennon, Alex Castillo, Pablo E McKnight, G Stanley |
author_sort | Jones, Brian W |
collection | PubMed |
description | Protein Kinase A (PKA) mediates synaptic plasticity and is widely implicated in learning and memory. The hippocampal dentate gyrus (DG) is thought to be responsible for processing and encoding distinct contextual associations in response to highly similar inputs. The mossy fiber (MF) axons of the dentate granule cells convey strong excitatory drive to CA3 pyramidal neurons and express presynaptic, PKA-dependent forms of plasticity. Here, we demonstrate an essential role for the PKA anchoring protein, AKAP7, in mouse MF axons and terminals. Genetic ablation of AKAP7 specifically from dentate granule cells results in disruption of MF-CA3 LTP directly initiated by cAMP, and the AKAP7 mutant mice are selectively deficient in pattern separation behaviors. Our results suggest that the AKAP7/PKA complex in the MF projections plays an essential role in synaptic plasticity and contextual memory formation. DOI: http://dx.doi.org/10.7554/eLife.20695.001 |
format | Online Article Text |
id | pubmed-5135391 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-51353912016-12-05 Targeted deletion of AKAP7 in dentate granule cells impairs spatial discrimination Jones, Brian W Deem, Jennifer Younts, Thomas J Weisenhaus, Michael Sanford, Christina A Slack, Margaret C Chin, Jenesa Nachmanson, Daniela McKennon, Alex Castillo, Pablo E McKnight, G Stanley eLife Neuroscience Protein Kinase A (PKA) mediates synaptic plasticity and is widely implicated in learning and memory. The hippocampal dentate gyrus (DG) is thought to be responsible for processing and encoding distinct contextual associations in response to highly similar inputs. The mossy fiber (MF) axons of the dentate granule cells convey strong excitatory drive to CA3 pyramidal neurons and express presynaptic, PKA-dependent forms of plasticity. Here, we demonstrate an essential role for the PKA anchoring protein, AKAP7, in mouse MF axons and terminals. Genetic ablation of AKAP7 specifically from dentate granule cells results in disruption of MF-CA3 LTP directly initiated by cAMP, and the AKAP7 mutant mice are selectively deficient in pattern separation behaviors. Our results suggest that the AKAP7/PKA complex in the MF projections plays an essential role in synaptic plasticity and contextual memory formation. DOI: http://dx.doi.org/10.7554/eLife.20695.001 eLife Sciences Publications, Ltd 2016-12-02 /pmc/articles/PMC5135391/ /pubmed/27911261 http://dx.doi.org/10.7554/eLife.20695 Text en © 2016, Jones et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Jones, Brian W Deem, Jennifer Younts, Thomas J Weisenhaus, Michael Sanford, Christina A Slack, Margaret C Chin, Jenesa Nachmanson, Daniela McKennon, Alex Castillo, Pablo E McKnight, G Stanley Targeted deletion of AKAP7 in dentate granule cells impairs spatial discrimination |
title | Targeted deletion of AKAP7 in dentate granule cells impairs spatial discrimination |
title_full | Targeted deletion of AKAP7 in dentate granule cells impairs spatial discrimination |
title_fullStr | Targeted deletion of AKAP7 in dentate granule cells impairs spatial discrimination |
title_full_unstemmed | Targeted deletion of AKAP7 in dentate granule cells impairs spatial discrimination |
title_short | Targeted deletion of AKAP7 in dentate granule cells impairs spatial discrimination |
title_sort | targeted deletion of akap7 in dentate granule cells impairs spatial discrimination |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5135391/ https://www.ncbi.nlm.nih.gov/pubmed/27911261 http://dx.doi.org/10.7554/eLife.20695 |
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