显性阴性DISC1改变小鼠前额叶皮层抑制性中间神经元的多巴胺能调节。

Molecular Neuropsychiatry Pub Date : 2018-06-01 Epub Date: 2018-05-07 DOI:10.1159/000488030
Ross A Cardarelli, Rolicia Martin, Hanna Jaaro-Peled, Akira Sawa, Elizabeth M Powell, Patricio O'Donnell
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引用次数: 6

摘要

精神分裂症1 (Disc1)基因的截断破坏增加了精神疾病的风险,可能影响皮质中间神经元。在这里,我们试图确定携带截断(Disc1)等位基因(DN-DISC1)的小鼠是否会影响该细胞群。我们利用全细胞记录来评估野生型和DN-DISC1小鼠两类中间神经元的电生理特性和多巴胺(DA)的调节:快速峰值(FS)和低阈值峰值(LTS)中间神经元。在DN-DISC1小鼠中,FS中间神经元而非LTS中间神经元表现出改变的动作电位。此外,在DN-DISC1小鼠中,围绕FS中间神经元的神经元周围网表现出异常形态,并且该细胞类型的DA调节在DN-DISC1小鼠中发生了改变。我们的结论是,生命早期对与精神疾病风险相关的基因的操作可能导致特定gaba能中间神经元的功能障碍,但不会丢失。由此引起的兴奋-抑制平衡的改变是DISC1病理生理的一个关键因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Dominant-Negative DISC1 Alters the Dopaminergic Modulation of Inhibitory Interneurons in the Mouse Prefrontal Cortex.

Dominant-Negative DISC1 Alters the Dopaminergic Modulation of Inhibitory Interneurons in the Mouse Prefrontal Cortex.

Dominant-Negative DISC1 Alters the Dopaminergic Modulation of Inhibitory Interneurons in the Mouse Prefrontal Cortex.

Dominant-Negative DISC1 Alters the Dopaminergic Modulation of Inhibitory Interneurons in the Mouse Prefrontal Cortex.

A truncated disrupted in schizophrenia 1 (Disc1) gene increases the risk of psychiatric disorders, probably affecting cortical interneurons. Here, we sought to determine whether this cell population is affected in mice carrying a truncated (Disc1) allele (DN-DISC1). We utilized whole cell recordings to assess electrophysiological properties and modulation by dopamine (DA) in two classes of interneurons: fast-spiking (FS) and low threshold-spiking (LTS) interneurons in wild-type and DN-DISC1 mice. In DN-DISC1 mice, FS interneurons, but not LTS interneurons, exhibited altered action potentials. Further, the perineuronal nets that surround FS interneurons exhibited abnormal morphology in DN-DISC1 mice, and the DA modulation of this cell type was altered in DN-DISC1 mice. We conclude that early-life manipulation of a gene associated with risk of psychiatric disease can result in dysfunction, but not loss, of specific GABAergic interneurons. The resulting alteration of excitatory-inhibitory balance is a critical element in DISC1 pathophysiology.

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