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dc.contributor.authorMizuta, Kotaroen
dc.contributor.authorNakai, Junichien
dc.contributor.authorHayashi, Yasunorien
dc.contributor.authorSato, Masaakien
dc.contributor.alternative水田, 恒太郎ja
dc.contributor.alternative中井, 淳一ja
dc.contributor.alternative林, 康紀ja
dc.contributor.alternative佐藤, 正晃ja
dc.date.accessioned2022-10-05T03:05:33Z-
dc.date.available2022-10-05T03:05:33Z-
dc.date.issued2021-03-
dc.identifier.urihttp://hdl.handle.net/2433/276574-
dc.description.abstractIn the hippocampus, spatial and nonspatial information are jointly represented as a neural map in which locations associated with salient features are over-represented by increased densities of relevant place cells. Although we recently demonstrated that experience-dependent establishment of these disproportionate maps is governed by selective stabilization of salient place cells following their conversion from non-place cells, the underlying mechanism for pre-established map reorganization remained to be understood. To this end, we investigated the changes in CA1 functional cellular maps imaged using two-photon calcium imaging in mice performing a reward-rearrangement task in virtual reality. Mice were pre-trained on a virtual linear track with a visual landmark and a reward in two distinct locations. Then, they were re-trained on the same track with the exception that the location of reward was shifted to match the landmark location. We found that, in contrast to de novo map formation, robust map reorganization occurred through parallel coordination of new place field formation, lateral shifting of existing place fields, and selective stabilization of place fields encoding salient locations. Our findings demonstrate that intricate interplay between multiple forms of cellular dynamics enables rapid updating of information stored in hippocampal maps.en
dc.language.isoeng-
dc.publisherWileyen
dc.rights© 2021 The Authors. Hippocampus published by Wiley Periodicals LLC.en
dc.rightsThis is an open access article under the terms of the Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.en
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/-
dc.subjectcalcium imagingen
dc.subjectcognitive mapen
dc.subjectnavigationen
dc.subjectspatial memoryen
dc.subjectvirtual realityen
dc.titleMultiple coordinated cellular dynamics mediate CA1 map plasticityen
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.jtitleHippocampusen
dc.identifier.volume31-
dc.identifier.issue3-
dc.identifier.spage235-
dc.identifier.epage243-
dc.relation.doi10.1002/hipo.23300-
dc.textversionpublisher-
dc.identifier.pmid33452849-
dcterms.accessRightsopen access-
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dc.identifier.pissn1050-9631-
dc.identifier.eissn1098-1063-
jpcoar.funderName日本学術振興会ja
jpcoar.funderName日本学術振興会ja
jpcoar.funderName日本学術振興会ja
jpcoar.funderName日本学術振興会ja
jpcoar.funderName日本学術振興会ja
jpcoar.funderName日本学術振興会ja
jpcoar.funderName日本学術振興会ja
jpcoar.funderName日本学術振興会ja
jpcoar.funderName日本学術振興会ja
jpcoar.funderName日本学術振興会ja
jpcoar.funderName日本学術振興会ja
jpcoar.funderName日本学術振興会ja
jpcoar.funderName日本学術振興会ja
jpcoar.funderName日本学術振興会ja
jpcoar.funderName日本学術振興会ja
jpcoar.awardTitleアルツハイマー病の微小回路可視化による破綻過程の解明ja
jpcoar.awardTitle進化工学を利用した蛍光プローブの開発研究ja
jpcoar.awardTitle記憶形成、固定、想起における海馬背側CA1セルアセンブリの長期可視化ja
jpcoar.awardTitle生物ナビゲーションのシステム同定と革新的ロギングデバイスの開発ja
jpcoar.awardTitleアルツハイマー病の神経回路長期可視化による機能破綻過程の解明ja
jpcoar.awardTitleマウスの社会性ナビゲーションの神経基盤の解明ja
jpcoar.awardTitle記憶固定における海馬から大脳皮質への情報のリレー機構ja
jpcoar.awardTitleシナプス操作によるPTSDの構成的理解ja
jpcoar.awardTitleマウス社会性ナビゲーションの多感覚仮想環境における再構成とその包括的理解ja
jpcoar.awardTitle報酬場所記憶に関わる場所細胞の形成メカニズムと機能的役割の解明ja
jpcoar.awardTitleセルアセンブリ形成メカニズムの構成的理解ja
jpcoar.awardTitle脳深部錐体細胞の反応特異性を決定する樹状突起スパイン活動の機能イメージングja
jpcoar.awardTitle行動動物脳深部神経回路の可視化技術の開発と神経回路の生理・病理下での安定性の研究ja
jpcoar.awardTitle仮想現実環境と二光子イメージング法を用いた海馬における物体と空間の記憶連関の研究ja
jpcoar.awardTitle運動学習における長期記憶機構の研究ja
出現コレクション:学術雑誌掲載論文等

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