Synaptic activity–dependent changes in the hippocampal palmitoylome

棕榈酰化 突触可塑性 长时程增强 生物 细胞生物学 突触后密度 突触疲劳 非突触性可塑性 神经科学 突触 突触增强 变质塑性 突触标度 化学 生物化学 受体 半胱氨酸
作者
Glory G Nasseri,Nusrat Matin,Angela R. Wild,Kira Tosefsky,Stéphane Flibotte,R. Greg Stacey,Rocio Hollman,Leonard J. Foster,Shernaz X. Bamji
出处
期刊:Science Signaling [American Association for the Advancement of Science]
卷期号:15 (763): eadd2519-eadd2519 被引量:26
标识
DOI:10.1126/scisignal.add2519
摘要

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.
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