{"database":"bioimages","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"submitter":[null],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-BIAD910"],"repository":["bioimages"],"figure_sub":["Specimen","Study Component","organisation","Biosample","Associations","Image acquisition"],"pubmed_authors":["Benjamin Cravatt","Nicolas Vitale","Alysee A. Michaels","Rachel S. Gormal","Bharat G. Venkatesh","Jesus Bertran-Gonzalez","Daniel G. Blackmore","Emma Sieriecki","Yann Gambin","Yann Humeau","Akefe Isaac Oluwatobi","Benjamin Matthews","Suzy Alexander","Mingshan Xue","Merja Joensuu","Sevannah Ellis","Tristan P. Wallis","Frédéric A. Meunier","Saber H. Saber"],"additional_accession":[]},"is_claimable":false,"name":"DDHD2 interacts with STXBP1 to mediate long-term memory via the generation of saturated free fatty acids","description":"Data for Immunofluorescence experiments - \nThe phospholipid and free fatty acid (FFA) composition of neuronal membranes plays a crucial role in learning and memory, but the mechanisms through which neuronal activity affects the brain's lipid landscape remain largely unexplored. Saturated FFAs, particularly myristic acid (C14:0), strongly increase during neuronal stimulation and memory acquisition, suggesting the involvement of phospholipase A1 (PLA1) activity in synaptic plasticity. Here, we show that genetic ablation of the DDHD2 isoform of PLA1 in mice markedly reduced saturated FFAs across the brain and memory performance in reward-based learning and spatial memory models prior to the development of neuromuscular deficits. DDHD2 was shown to bind to the key synaptic protein STXBP1. Usin","dates":{"release":"2023-11-04T00:00:00Z","modification":"2023-11-04T17:29:36.028Z","creation":"2023-11-04T17:29:36.028Z"},"accession":"S-BIAD910","cross_references":{}}