Cardarelli Ross A, Martin Rolicia, Jaaro-Peled Hanna, Sawa Akira, Powell Elizabeth M, O'Donnell Patricio
Program in Neuroscience, University of Maryland Medical School, Baltimore, Maryland, USA.
Department of Anatomy and Neurobiology, University of Maryland Medical School, Baltimore, Maryland, USA.
Mol Neuropsychiatry. 2018 Jun;4(1):20-29. doi: 10.1159/000488030. Epub 2018 May 7.
A truncated () 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 () 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.
一个截短的()基因会增加患精神疾病的风险,可能影响皮质中间神经元。在此,我们试图确定在携带截短的()等位基因(DN-DISC1)的小鼠中,这一细胞群体是否受到影响。我们利用全细胞记录来评估野生型和DN-DISC1小鼠中两类中间神经元(快速发放(FS)和低阈值发放(LTS)中间神经元)的电生理特性以及多巴胺(DA)对其的调节作用。在DN-DISC1小鼠中,FS中间神经元而非LTS中间神经元表现出动作电位改变。此外,在DN-DISC1小鼠中,围绕FS中间神经元的神经周网呈现出异常形态,并且该细胞类型的DA调节在DN-DISC1小鼠中发生了改变。我们得出结论,对与精神疾病风险相关基因的早期操纵可导致特定GABA能中间神经元功能障碍而非丧失。由此导致的兴奋性-抑制性平衡改变是DISC1病理生理学中的关键因素。