{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Ferrer-Ferrer M"],"funding":["DFG","FP7 People: Marie-Curie Actions","Deutsches Zentrum für Neurodegenerative Erkrankungen e.V. (DZNE) in der Helmholtz-Gemeinschaft"],"pagination":["82"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC9986217"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["80(4)"],"pubmed_abstract":["Neurotrypsin (NT) is a neuronal trypsin-like serine protease whose mutations cause severe mental retardation in humans. NT is activated in vitro by Hebbian-like conjunction of pre- and postsynaptic activities, which promotes the formation of dendritic filopodia via proteolytic cleavage of the proteoglycan agrin. Here, we investigated the functional importance of this mechanism for synaptic plasticity, learning, and extinction of memory. We report that juvenile neurotrypsin-deficient (NT<sup>-/-</sup>) mice exhibit impaired long-term potentiation induced by a spaced stimulation protocol designed to probe the generation of new filopodia and their conversion into functional synapses. Behaviorally, juvenile NT<sup>-/-</sup> mice show impaired contextual fear memory and have a sociability defic"],"journal":["Cellular and molecular life sciences : CMLS"],"pubmed_title":["Mice deficient in synaptic protease neurotrypsin show impaired spaced long-term potentiation and blunted learning-induced modulation of dendritic spines."],"pmcid":["PMC9986217"],"funding_grant_id":["6950 (Initial Training Network EXTRABRAIN)","Research Training Group 2413 SynAGE","FR 2758/3-1"],"pubmed_authors":["Senkov O","Safari M","Jia S","Kaushik R","Frischknecht R","Dityatev A","Ferrer-Ferrer M","Schneeberg J","Aleshin S","Wlodarczyk J","Mironov A","Figiel I"],"additional_accession":[]},"is_claimable":false,"name":"Mice deficient in synaptic protease neurotrypsin show impaired spaced long-term potentiation and blunted learning-induced modulation of dendritic spines.","description":"Neurotrypsin (NT) is a neuronal trypsin-like serine protease whose mutations cause severe mental retardation in humans. NT is activated in vitro by Hebbian-like conjunction of pre- and postsynaptic activities, which promotes the formation of dendritic filopodia via proteolytic cleavage of the proteoglycan agrin. Here, we investigated the functional importance of this mechanism for synaptic plasticity, learning, and extinction of memory. We report that juvenile neurotrypsin-deficient (NT<sup>-/-</sup>) mice exhibit impaired long-term potentiation induced by a spaced stimulation protocol designed to probe the generation of new filopodia and their conversion into functional synapses. Behaviorally, juvenile NT<sup>-/-</sup> mice show impaired contextual fear memory and have a sociability defic","dates":{"release":"2023-01-01T00:00:00Z","publication":"2023 Mar","modification":"2026-07-14T19:05:31.09Z","creation":"2025-04-07T03:18:53.175Z"},"accession":"S-EPMC9986217","cross_references":{"pubmed":["36871239"],"doi":["10.1007/s00018-023-04720-z"]}}