Disrupted Place Cell Remapping and Impaired Grid Cells in a Knockin Model of Alzheimer's Disease.


Journal

Neuron
ISSN: 1097-4199
Titre abrégé: Neuron
Pays: United States
ID NLM: 8809320

Informations de publication

Date de publication:
23 09 2020
Historique:
received: 01 11 2019
revised: 13 03 2020
accepted: 22 06 2020
pubmed: 23 7 2020
medline: 21 11 2020
entrez: 23 7 2020
Statut: ppublish

Résumé

Patients with Alzheimer's disease (AD) suffer from spatial memory impairment and wandering behavior, but the brain circuit mechanisms causing such symptoms remain largely unclear. In healthy brains, spatially tuned hippocampal place cells and entorhinal grid cells exhibit distinct spike patterns in different environments, a circuit function called "remapping." We tested remapping in amyloid precursor protein knockin (APP-KI) mice with impaired spatial memory. CA1 neurons, including place cells, showed disrupted remapping, although their spatial tuning was only mildly diminished. Medial entorhinal cortex (MEC) neurons severely lost their spatial tuning and grid cells were almost absent. Fast gamma oscillatory coupling between the MEC and CA1 was also impaired. Mild disruption of MEC grid cells emerged in younger APP-KI mice, although the spatial memory and CA1 remapping of the animals remained intact. These results point to remapping impairment in the hippocampus, possibly linked to grid cell disruption, as circuit mechanisms underlying spatial memory impairment in AD.

Identifiants

pubmed: 32697942
pii: S0896-6273(20)30477-3
doi: 10.1016/j.neuron.2020.06.023
pmc: PMC7529950
mid: NIHMS1608607
pii:
doi:

Substances chimiques

APP protein, mouse 0
Amyloid beta-Protein Precursor 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1095-1112.e6

Subventions

Organisme : NIGMS NIH HHS
ID : T32 GM008620
Pays : United States
Organisme : NIMH NIH HHS
ID : R01 MH121736
Pays : United States
Organisme : NIA NIH HHS
ID : F31 AG069500
Pays : United States
Organisme : NIA NIH HHS
ID : R01 AG063864
Pays : United States
Organisme : NIA NIH HHS
ID : R01 AG066806
Pays : United States

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Interests The authors declare no competing interests.

Auteurs

Heechul Jun (H)

Department of Anatomy and Neurobiology, University of California, Irvine, Irvine, CA, USA; Center for the Neurobiology of Learning and Memory, University of California, Irvine, Irvine, CA, USA; Institute for Memory Impairments and Neurological Disorders, University of California, Irvine, Irvine, CA, USA. Electronic address: heechulj@hs.uci.edu.

Allen Bramian (A)

Department of Anatomy and Neurobiology, University of California, Irvine, Irvine, CA, USA.

Shogo Soma (S)

Department of Anatomy and Neurobiology, University of California, Irvine, Irvine, CA, USA.

Takashi Saito (T)

Lab for Proteolytic Neuroscience, RIKEN Center for Brain Science, Wako, Saitama 351-0106, Japan.

Takaomi C Saido (TC)

Lab for Proteolytic Neuroscience, RIKEN Center for Brain Science, Wako, Saitama 351-0106, Japan.

Kei M Igarashi (KM)

Department of Anatomy and Neurobiology, University of California, Irvine, Irvine, CA, USA; Center for the Neurobiology of Learning and Memory, University of California, Irvine, Irvine, CA, USA; Institute for Memory Impairments and Neurological Disorders, University of California, Irvine, Irvine, CA, USA; Japan Science and Technology Agency, Tokyo, Japan. Electronic address: kei.igarashi@uci.edu.

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Classifications MeSH