Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, Campus Gualtar, 4710-057 Braga, Portugal; ICVS/3B's - PT Government Associate Laboratory, Braga/Guimarães, Portugal.
Department of Pathology and Cell Biology, Columbia University Medical Center, New York, NY 10032, USA.
Cell Rep. 2020 Mar 24;30(12):4197-4208.e6. doi: 10.1016/j.celrep.2020.02.102.
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.
磷脂酸(PA)是一种参与调节突触结构和功能的信号脂质。基于先前的研究表明,在啮齿动物海马体的纵轴上,PA 梯度逐渐降低,我们想知道背侧海马体(DH)和腹侧海马体(VH)是否受到 PA 调节的差异影响。在这里,我们发现与 PLD2 相比,磷脂酶 D1(PLD1)是海马体中 PA 的主要来源,并且 PLD1 缺失主要影响 DH 的脂质组。此外,Pld1 敲除(KO)小鼠在新物体识别和社交互动方面表现出特定缺陷,并且 CA1/CA3 锥体神经元的 DH-VH 树突分支分化受到干扰。此外,Pld1 KO 动物在 DH 中表现出 LTD 诱导减少以及 GluN2A 和 SNAP-25 蛋白水平降低。总的来说,我们观察到 PLD1 衍生的 PA 减少导致沿着海马体纵轴的不同脂质特征,主要影响 DH 的组织和功能。