{"PubmedArticle":{"MedlineCitation":{"@attributes":{"Status":"MEDLINE","Owner":"NLM","IndexingMethod":"Manual"},"PMID":{"@attributes":{"Version":"1"},"@text":"32948689"},"DateCompleted":{"Year":"2020","Month":"11","Day":"24"},"DateRevised":{"Year":"2023","Month":"03","Day":"14"},"Article":{"@attributes":{"PubModel":"Print-Electronic"},"Journal":{"ISSN":{"@attributes":{"IssnType":"Electronic"},"@text":"1091-6490"},"JournalIssue":{"@attributes":{"CitedMedium":"Internet"},"Volume":"117","Issue":"40","PubDate":{"Year":"2020","Month":"Oct","Day":"06"}},"Title":"Proceedings of the National Academy of Sciences of the United States of America","ISOAbbreviation":"Proc Natl Acad Sci U S A"},"ArticleTitle":"GRIP1 regulates synaptic plasticity and learning and memory.","Pagination":{"StartPage":"25085","EndPage":"25091","MedlinePgn":"25085-25091"},"ELocationID":[{"@attributes":{"EIdType":"doi","ValidYN":"Y"},"@text":"10.1073\/pnas.2014827117"}],"Abstract":{"AbstractText":["Hebbian plasticity is a key mechanism for higher brain functions, such as learning and memory. This form of synaptic plasticity primarily involves the regulation of synaptic \u03b1-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor (AMPAR) abundance and properties, whereby AMPARs are inserted into synapses during long-term potentiation (LTP) or removed during long-term depression (LTD). The molecular mechanisms underlying AMPAR trafficking remain elusive, however. Here we show that glutamate receptor interacting protein 1 (GRIP1), an AMPAR-binding protein shown to regulate the trafficking and synaptic targeting of AMPARs, is required for LTP and learning and memory. GRIP1 is recruited into synapses during LTP, and deletion of <i>Grip1<\/i> in neurons blocks synaptic AMPAR accumulation induced by glycine-mediated depolarization. In addition, <i>Grip1<\/i> knockout mice exhibit impaired hippocampal LTP, as well as deficits in learning and memory. Mechanistically, we find that phosphorylation of serine-880 of the GluA2 AMPAR subunit (GluA2-S880) is decreased while phosphorylation of tyrosine-876 on GluA2 (GluA2-Y876) is elevated during chemically induced LTP. This enhances the strength of the GRIP1-AMPAR association and, subsequently, the insertion of AMPARs into the postsynaptic membrane. Together, these results demonstrate an essential role of GRIP1 in regulating AMPAR trafficking during synaptic plasticity and learning and memory."]},"AuthorList":{"@attributes":{"CompleteYN":"Y"},"Author":[{"@attributes":{"ValidYN":"Y"},"LastName":"Tan","ForeName":"Han L","Initials":"HL","Identifier":[{"@attributes":{"Source":"ORCID"},"@text":"0000-0001-5163-7720"}],"AffiliationInfo":[{"Affiliation":"Solomon H. Snyder Department of Neuroscience and Kavli Neuroscience Discovery Institute, Johns Hopkins University School of Medicine, Baltimore, MD 21205."}]},{"@attributes":{"ValidYN":"Y"},"LastName":"Chiu","ForeName":"Shu-Ling","Initials":"SL","Identifier":[{"@attributes":{"Source":"ORCID"},"@text":"0000-0003-4429-7830"}],"AffiliationInfo":[{"Affiliation":"Solomon H. Snyder Department of Neuroscience and Kavli Neuroscience Discovery Institute, Johns Hopkins University School of Medicine, Baltimore, MD 21205."},{"Affiliation":"Institute of Cellular and Organismic Biology, Academia Sinica, 11529 Taipei, Taiwan."}]},{"@attributes":{"ValidYN":"Y"},"LastName":"Zhu","ForeName":"Qianwen","Initials":"Q","Identifier":[{"@attributes":{"Source":"ORCID"},"@text":"0000-0003-2799-2372"}],"AffiliationInfo":[{"Affiliation":"Solomon H. Snyder Department of Neuroscience and Kavli Neuroscience Discovery Institute, Johns Hopkins University School of Medicine, Baltimore, MD 21205."}]},{"@attributes":{"ValidYN":"Y"},"LastName":"Huganir","ForeName":"Richard L","Initials":"RL","Identifier":[{"@attributes":{"Source":"ORCID"},"@text":"0000-0001-9783-5183"}],"AffiliationInfo":[{"Affiliation":"Solomon H. Snyder Department of Neuroscience and Kavli Neuroscience Discovery Institute, Johns Hopkins University School of Medicine, Baltimore, MD 21205; rhuganir@jhmi.edu."}]}]},"Language":["eng"],"GrantList":{"@attributes":{"CompleteYN":"Y"},"Grant":[{"GrantID":"R01 MH112808","Acronym":"MH","Agency":"NIMH NIH HHS","Country":"United States"},{"GrantID":"R01 NS036715","Acronym":"NS","Agency":"NINDS NIH HHS","Country":"United States"},{"GrantID":"R37 NS036715","Acronym":"NS","Agency":"NINDS NIH HHS","Country":"United States"}]},"PublicationTypeList":{"PublicationType":[{"@attributes":{"UI":"D016428"},"@text":"Journal Article"},{"@attributes":{"UI":"D052061"},"@text":"Research Support, N.I.H., Extramural"}]},"ArticleDate":[{"@attributes":{"DateType":"Electronic"},"Year":"2020","Month":"09","Day":"18"}]},"MedlineJournalInfo":{"Country":"United States","MedlineTA":"Proc Natl Acad Sci U S 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receptor ionotropic, AMPA 2"}}]},"CitationSubset":["IM"],"MeshHeadingList":{"MeshHeading":[{"DescriptorName":{"@attributes":{"UI":"D048868","MajorTopicYN":"N"},"@text":"Adaptor Proteins, Signal Transducing"},"QualifierName":[{"@attributes":{"UI":"Q000235","MajorTopicYN":"Y"},"@text":"genetics"}]},{"DescriptorName":{"@attributes":{"UI":"D000818","MajorTopicYN":"N"},"@text":"Animals"}},{"DescriptorName":{"@attributes":{"UI":"D002352","MajorTopicYN":"N"},"@text":"Carrier Proteins"},"QualifierName":[{"@attributes":{"UI":"Q000235","MajorTopicYN":"N"},"@text":"genetics"}]},{"DescriptorName":{"@attributes":{"UI":"D005786","MajorTopicYN":"N"},"@text":"Gene Expression 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