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024 7 _ |a 10.1016/j.celrep.2024.114112
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037 _ _ |a DZNE-2024-00529
082 _ _ |a 610
100 1 _ |a Chelini, Gabriele
|b 0
245 _ _ |a Focal clusters of peri-synaptic matrix contribute to activity-dependent plasticity and memory in mice
260 _ _ |a [New York, NY]
|c 2024
|b Elsevier
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520 _ _ |a Recent findings show that effective integration of novel information in the brain requires coordinated processes of homo- and heterosynaptic plasticity. In this work, we hypothesize that activity-dependent remodeling of the peri-synaptic extracellular matrix (ECM) contributes to these processes. We show that clusters of the peri-synaptic ECM, recognized by CS56 antibody, emerge in response to sensory stimuli, showing temporal and spatial coincidence with dendritic spine plasticity. Using CS56 co-immunoprecipitation of synaptosomal proteins, we identify several molecules involved in Ca2+ signaling, vesicle cycling, and AMPA-receptor exocytosis, thus suggesting a role in long-term potentiation (LTP). Finally, we show that, in the CA1 hippocampal region, the attenuation of CS56 glycoepitopes, through the depletion of versican as one of its main carriers, impairs LTP and object location memory in mice. These findings show that activity-dependent remodeling of the peri-synaptic ECM regulates the induction and consolidation of LTP, contributing to hippocampal-dependent memory.
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650 _ 7 |a CP: Cell biology
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650 _ 7 |a CP: Neuroscience
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650 _ 7 |a CS clusters
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650 _ 7 |a chondrotin sulfate proteoglycans
|2 Other
650 _ 7 |a extracellular matrix
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650 _ 7 |a hippocampus
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650 _ 7 |a immunoprecipitation
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650 _ 7 |a learning and memory
|2 Other
650 _ 7 |a sensory manipulation
|2 Other
650 _ 7 |a synaptic plasticity
|2 Other
650 _ 7 |a versican
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650 _ 2 |a Animals
|2 MeSH
650 _ 2 |a Extracellular Matrix: metabolism
|2 MeSH
650 _ 2 |a Long-Term Potentiation: physiology
|2 MeSH
650 _ 2 |a Mice
|2 MeSH
650 _ 2 |a Neuronal Plasticity: physiology
|2 MeSH
650 _ 2 |a Memory: physiology
|2 MeSH
650 _ 2 |a Synapses: metabolism
|2 MeSH
650 _ 2 |a Synapses: physiology
|2 MeSH
650 _ 2 |a Mice, Inbred C57BL
|2 MeSH
650 _ 2 |a Male
|2 MeSH
650 _ 2 |a CA1 Region, Hippocampal: metabolism
|2 MeSH
650 _ 2 |a CA1 Region, Hippocampal: physiology
|2 MeSH
650 _ 2 |a CA1 Region, Hippocampal: cytology
|2 MeSH
650 _ 2 |a Hippocampus: metabolism
|2 MeSH
650 _ 2 |a Hippocampus: physiology
|2 MeSH
700 1 _ |a Mirzapourdelavar, Hadi
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700 1 _ |a Durning, Peter
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700 1 _ |a Baidoe-Ansah, David
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700 1 _ |a Sethi, Manveen K.
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700 1 _ |a O’Donovan, Sinead M.
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700 1 _ |a Klengel, Torsten
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700 1 _ |a Balasco, Luigi
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700 1 _ |a Berciu, Cristina
|b 8
700 1 _ |a Boyer-Boiteau, Anne
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700 1 _ |a McCullumsmith, Robert
|b 10
700 1 _ |a Ressler, Kerry J.
|b 11
700 1 _ |a Zaia, Joseph
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700 1 _ |a Bozzi, Yuri
|b 13
700 1 _ |a Dityatev, Alexander
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700 1 _ |a Berretta, Sabina
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773 _ _ |a 10.1016/j.celrep.2024.114112
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910 1 _ |a Deutsches Zentrum für Neurodegenerative Erkrankungen
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