Literature DB >> 31056352

Time Cells in the Hippocampus Are Neither Dependent on Medial Entorhinal Cortex Inputs nor Necessary for Spatial Working Memory.

Marta Sabariego1, Antonia Schönwald1, Brittney L Boublil1, David T Zimmerman1, Siavash Ahmadi1, Nailea Gonzalez1, Christian Leibold2, Robert E Clark3, Jill K Leutgeb1, Stefan Leutgeb4.   

Abstract

A key function of the hippocampus and entorhinal cortex is to bridge events that are discontinuous in time, and it has been proposed that medial entorhinal cortex (mEC) supports memory retention by sustaining the sequential activity of hippocampal time cells. Therefore, we recorded hippocampal neuronal activity during spatial working memory and asked whether time cells depend on mEC inputs. Working memory was impaired in rats with mEC lesions, but the occurrence of time cells and of trajectory-coding cells in the stem did not differ from controls. Rather, the main effect of mEC lesions was an extensive spatial coding deficit of CA1 cells, which included inconsistency over time and reduced firing differences between positions on the maze. Therefore, mEC is critical for providing stable and distinct spatial information to hippocampus, while working memory (WM) maintenance is likely supported either by local synaptic plasticity in hippocampus or by activity patterns elsewhere in the brain.
Copyright © 2019 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  hippocampus; medial entorhinal cortex; place cells; time cells; working memory

Mesh:

Year:  2019        PMID: 31056352      PMCID: PMC6602601          DOI: 10.1016/j.neuron.2019.04.005

Source DB:  PubMed          Journal:  Neuron        ISSN: 0896-6273            Impact factor:   17.173


  73 in total

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4.  Trajectory encoding in the hippocampus and entorhinal cortex.

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8.  Impaired recognition memory in rats after damage to the hippocampus.

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Authors:  E R Wood; P A Dudchenko; R J Robitsek; H Eichenbaum
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Review 4.  Navigating Through Time: A Spatial Navigation Perspective on How the Brain May Encode Time.

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6.  Inactivation of the Medial Entorhinal Cortex Selectively Disrupts Learning of Interval Timing.

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8.  Modality-Specific Impairment of Hippocampal CA1 Neurons of Alzheimer's Disease Model Mice.

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9.  Crucial role for CA2 inputs in the sequential organization of CA1 time cells supporting memory.

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