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Synaptic activity–dependent changes in the hippocampal palmitoylome

Glory G Nasseri, Nusrat Matin, Angela R. Wild, Kira Tosefsky, Stéphane Flibotte, R. Greg Stacey, Rocio Hollman, Leonard J. Foster, Shernaz X. Bamji

2022Science Signaling32 citationsDOI

Abstract

Dynamic protein S-palmitoylation is critical for neuronal function, development, and synaptic plasticity. Synaptic activity-dependent changes in palmitoylation have been reported for a small number of proteins. Here, we characterized the palmitoylome in the hippocampi of male mice before and after context-dependent fear conditioning. Of the 121 differentially palmitoylated proteins identified, just over half were synaptic proteins, whereas others were associated with metabolic functions, cytoskeletal organization, and signal transduction. The synapse-associated proteins generally exhibited increased palmitoylation after fear conditioning. In contrast, most of the proteins that exhibited decreased palmitoylation were associated with metabolic processes. Similar results were seen in cultured rat hippocampal neurons in response to chemically induced long-term potentiation. Furthermore, we found that the palmitoylation of one of the synaptic proteins, plasticity-related gene-1 (PRG-1), also known as lipid phosphate phosphatase-related protein type 4 (LPPR4), was important for synaptic activity-induced insertion of α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptors (AMPARs) into the postsynaptic membrane. The findings identify proteins whose dynamic palmitoylation may regulate their role in synaptic plasticity, learning, and memory.

Topics & Concepts

PalmitoylationSynaptic plasticityLong-term potentiationBiologyCell biologyNeuroscienceSynaptic fatigueNonsynaptic plasticityPostsynaptic densitySynapseMetaplasticitySynaptic augmentationSynaptic scalingChemistryBiochemistryReceptorCysteineEnzymeReceptor Mechanisms and SignalingNeuroscience and Neuropharmacology ResearchNeuropeptides and Animal Physiology
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