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抑制 14-3-3 蛋白可增加小鼠海马 CA1 锥体神经元的固有兴奋性。

Inhibition of 14-3-3 proteins increases the intrinsic excitability of mouse hippocampal CA1 pyramidal neurons.

机构信息

Biomedical Sciences Department, College of Medicine, Florida State University, Tallahassee, Florida, USA.

出版信息

Eur J Neurosci. 2024 Jun;59(12):3309-3321. doi: 10.1111/ejn.16349. Epub 2024 Apr 22.

Abstract

14-3-3 proteins are a family of regulatory proteins that are abundantly expressed in the brain and enriched at the synapse. Dysfunctions of these proteins have been linked to neurodevelopmental and neuropsychiatric disorders. Our group has previously shown that functional inhibition of these proteins by a peptide inhibitor, difopein, in the mouse brain causes behavioural alterations and synaptic plasticity impairment in the hippocampus. Recently, we found an increased cFOS expression in difopein-expressing dorsal CA1 pyramidal neurons, indicating enhanced neuronal activity by 14-3-3 inhibition in these cells. In this study, we used slice electrophysiology to determine the effects of 14-3-3 inhibition on the intrinsic excitability of CA1 pyramidal neurons from a transgenic 14-3-3 functional knockout (FKO) mouse line. Our data demonstrate an increase in intrinsic excitability associated with 14-3-3 inhibition, as well as reveal action potential firing pattern shifts after novelty-induced hyperlocomotion in the 14-3-3 FKO mice. These results provide novel information on the role 14-3-3 proteins play in regulating intrinsic and activity-dependent neuronal excitability in the hippocampus.

摘要

14-3-3 蛋白是一类调节蛋白,在大脑中大量表达,并在突触处富集。这些蛋白的功能障碍与神经发育和神经精神疾病有关。我们的研究小组之前曾表明,在小鼠大脑中,一种肽抑制剂 difopein 对这些蛋白的功能抑制会导致海马体中的行为改变和突触可塑性损伤。最近,我们发现表达 difopein 的背侧 CA1 锥体神经元中 cFOS 表达增加,这表明这些细胞中的 14-3-3 抑制增强了神经元活性。在这项研究中,我们使用切片电生理学来确定 14-3-3 抑制对来自转基因 14-3-3 功能缺失(FKO)小鼠系的 CA1 锥体神经元内在兴奋性的影响。我们的数据表明,14-3-3 抑制与内在兴奋性增加有关,并且在 14-3-3 FKO 小鼠新奇诱导的过度活跃后揭示了动作电位发放模式的转变。这些结果为 14-3-3 蛋白在调节海马体中内在和活动依赖性神经元兴奋性方面的作用提供了新的信息。

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