Phospholipase D1 Ablation Disrupts Mouse Longitudinal Hippocampal Axis Organization and Functioning
Author(s) -
Luísa Santa-Marinha,
Isabel Castanho,
Rita Ribeiro Silva,
Francisca Vaz Bravo,
André Miguel Miranda,
Torcato Meira,
Rafaela MoraisRibeiro,
Fernanda Marques,
Yimeng Xu,
Kimberly Point du Jour,
Markus R. Wenk,
Robin Chan,
Gilbert Di Paolo,
Vítor Pinto,
Tiago Gil Oliveira
Publication year - 2020
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2020.02.102
Subject(s) - hippocampal formation , hippocampus , lipidome , neuroscience , phospholipase d , chemistry , microbiology and biotechnology , phosphatidic acid , endocrinology , biology , medicine , biochemistry , signal transduction , lipid metabolism , phospholipid , membrane
Phosphatidic acid (PA) is a signaling lipid involved in the modulation of synaptic structure and functioning. Based on previous work showing a decreasing PA gradient along the longitudinal axis of the rodent hippocampus, we asked whether the dorsal hippocampus (DH) and the ventral hippocampus (VH) are differentially affected by PA modulation. Here, we show that phospholipase D1 (PLD1) is a major hippocampal PA source, compared to PLD2, and that PLD1 ablation affects predominantly the lipidome of the DH. Moreover, Pld1 knockout (KO) mice show specific deficits in novel object recognition and social interaction and disruption in the DH-VH dendritic arborization differentiation in CA1/CA3 pyramidal neurons. Also, Pld1 KO animals present reduced long-term depression (LTD) induction and reduced GluN2A and SNAP-25 protein levels in the DH. Overall, we observe that PLD1-derived PA reduction leads to differential lipid signatures along the longitudinal hippocampal axis, predominantly affecting DH organization and functioning.
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