Impaired path integration and grid cell spatial periodicity in mice lacking GluA1-containing AMPA receptors

The hippocampus and the parahippocampal region have been proposed to contribute to path integration. Mice lacking GluA1-containing AMPA receptors (GluA1(-/-) mice) were previously shown to exhibit impaired hippocampal place cell selectivity. Here we investigated whether path integration performance...

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Published in:The Journal of neuroscience Vol. 34; no. 18; pp. 6245 - 6259
Main Authors: Allen, Kevin, Gil, Mariana, Resnik, Evgeny, Toader, Oana, Seeburg, Peter, Monyer, Hannah
Format: Journal Article
Language:English
Published: United States Society for Neuroscience 30-04-2014
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Abstract The hippocampus and the parahippocampal region have been proposed to contribute to path integration. Mice lacking GluA1-containing AMPA receptors (GluA1(-/-) mice) were previously shown to exhibit impaired hippocampal place cell selectivity. Here we investigated whether path integration performance and the activity of grid cells of the medial entorhinal cortex (MEC) are affected in these mice. We first tested GluA1(-/-) mice on a standard food-carrying homing task and found that they were impaired in processing idiothetic cues. To corroborate these findings, we developed an L-maze task that is less complex and is performed entirely in darkness, thereby reducing numerous confounding variables when testing path integration. Also in this task, the performance of GluA1(-/-) mice was impaired. Next, we performed in vivo recordings in the MEC of GluA1(-/-) mice. MEC neurons exhibited altered grid cell spatial periodicity and reduced spatial selectivity, whereas head direction tuning and speed modulation were not affected. The firing associations between pairs of neurons in GluA1(-/-) mice were stable, both in time and space, indicating that attractor states were still present despite the lack of grid periodicity. Together, these results support the hypothesis that spatial representations in the hippocampal-entorhinal network contribute to path integration.
AbstractList The hippocampus and the parahippocampal region have been proposed to contribute to path integration. Mice lacking GluA1-containing AMPA receptors ( GluA1 −/− mice) were previously shown to exhibit impaired hippocampal place cell selectivity. Here we investigated whether path integration performance and the activity of grid cells of the medial entorhinal cortex (MEC) are affected in these mice. We first tested GluA1 −/− mice on a standard food-carrying homing task and found that they were impaired in processing idiothetic cues. To corroborate these findings, we developed an L-maze task that is less complex and is performed entirely in darkness, thereby reducing numerous confounding variables when testing path integration. Also in this task, the performance of GluA1 −/− mice was impaired. Next, we performed in vivo recordings in the MEC of GluA1 −/− mice. MEC neurons exhibited altered grid cell spatial periodicity and reduced spatial selectivity, whereas head direction tuning and speed modulation were not affected. The firing associations between pairs of neurons in GluA1 −/− mice were stable, both in time and space, indicating that attractor states were still present despite the lack of grid periodicity. Together, these results support the hypothesis that spatial representations in the hippocampal–entorhinal network contribute to path integration.
The hippocampus and the parahippocampal region have been proposed to contribute to path integration. Mice lacking GluA1-containing AMPA receptors (GluA1 super(-/-) mice) were previously shown to exhibit impaired hippocampal place cell selectivity. Here we investigated whether path integration performance and the activity of grid cells of the medial entorhinal cortex (MEC) are affected in these mice. We first tested GluA1 super(-/-) mice on a standard food-carrying homing task and found that they were impaired in processing idiothetic cues. To corroborate these findings, we developed an L-maze task that is less complex and is performed entirely in darkness, thereby reducing numerous confounding variables when testing path integration. Also in this task, the performance of GluA1 super(-/-) mice was impaired. Next, we performed in vivo recordings in the MEC of GluA1 super(-/-) mice. MEC neurons exhibited altered grid cell spatial periodicity and reduced spatial selectivity, whereas head direction tuning and speed modulation were not affected. The firing associations between pairs of neurons in GluA1 super(-/-) mice were stable, both in time and space, indicating that attractor states were still present despite the lack of grid periodicity. Together, these results support the hypothesis that spatial representations in the hippocampal-entorhinal network contribute to path integration.
The hippocampus and the parahippocampal region have been proposed to contribute to path integration. Mice lacking GluA1-containing AMPA receptors (GluA1(-/-) mice) were previously shown to exhibit impaired hippocampal place cell selectivity. Here we investigated whether path integration performance and the activity of grid cells of the medial entorhinal cortex (MEC) are affected in these mice. We first tested GluA1(-/-) mice on a standard food-carrying homing task and found that they were impaired in processing idiothetic cues. To corroborate these findings, we developed an L-maze task that is less complex and is performed entirely in darkness, thereby reducing numerous confounding variables when testing path integration. Also in this task, the performance of GluA1(-/-) mice was impaired. Next, we performed in vivo recordings in the MEC of GluA1(-/-) mice. MEC neurons exhibited altered grid cell spatial periodicity and reduced spatial selectivity, whereas head direction tuning and speed modulation were not affected. The firing associations between pairs of neurons in GluA1(-/-) mice were stable, both in time and space, indicating that attractor states were still present despite the lack of grid periodicity. Together, these results support the hypothesis that spatial representations in the hippocampal-entorhinal network contribute to path integration.
Author Toader, Oana
Seeburg, Peter
Allen, Kevin
Monyer, Hannah
Resnik, Evgeny
Gil, Mariana
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  surname: Allen
  fullname: Allen, Kevin
  organization: Department of Clinical Neurobiology, Medical Faculty of Heidelberg University and German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany, and Department of Molecular Neurobiology, Max Planck Institute of Medical Research, 69120 Heidelberg, Germany
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  givenname: Mariana
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Keywords entorhinal cortex
grid cells
navigation
hippocampus
path integration
glutamate receptors
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K.A. and M.G. contributed equally to this work.
Author contributions: K.A., M.G., E.R., P.S., and H.M. designed research; K.A., M.G., E.R., and O.T. performed research; K.A., M.G., and O.T. analyzed data; K.A., M.G., P.S., and H.M. wrote the paper.
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Snippet The hippocampus and the parahippocampal region have been proposed to contribute to path integration. Mice lacking GluA1-containing AMPA receptors (GluA1(-/-)...
The hippocampus and the parahippocampal region have been proposed to contribute to path integration. Mice lacking GluA1-containing AMPA receptors ( GluA1 −/−...
The hippocampus and the parahippocampal region have been proposed to contribute to path integration. Mice lacking GluA1-containing AMPA receptors (GluA1...
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pubmed
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StartPage 6245
SubjectTerms Acoustic Stimulation
Action Potentials - genetics
Animals
Brain Mapping
Cluster Analysis
Entorhinal Cortex - cytology
Homing Behavior - physiology
Male
Maze Learning - physiology
Mice
Mice, Transgenic
Models, Neurological
Neural Pathways - physiology
Neurons - physiology
Periodicity
Receptors, AMPA - deficiency
Receptors, AMPA - genetics
Space Perception - physiology
Spatial Behavior - physiology
Theta Rhythm
Time Factors
Title Impaired path integration and grid cell spatial periodicity in mice lacking GluA1-containing AMPA receptors
URI https://www.ncbi.nlm.nih.gov/pubmed/24790195
https://search.proquest.com/docview/1521324638
https://search.proquest.com/docview/1827922518
https://pubmed.ncbi.nlm.nih.gov/PMC6608102
Volume 34
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