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Attenuated bidirectional short-term synaptic plasticity in the dentate gyrus of Schnurri-2 knockout mice a model of schizophrenia

机译:Schnurri-2基因敲除小鼠的齿状回双向短期突触可塑性的减弱精神分裂症的模型

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摘要

The dentate gyrus of the hippocampus has been implicated in the pathophysiological basis of neuropsychiatric disorders including schizophrenia. We have identified several mouse models of neuropsychiatric disorders with robust molecular and functional defects in the dentate gyrus. Among them, mice lacking Schnurri-2 (Shn2 or HIVEP2) have been proposed as a model of schizophrenia and intellectual disability. Shn2 knockout mice exhibit behavioral abnormalities resembling symptoms of schizophrenia and HIVEP2-related intellectual disability as well as marked functional alterations in the soma and output synapse of the dentate granule cells (GCs). Although robust abnormalities were also observed in the dendritic spine morphology in the GCs, their functional correlates remain unknown. In the present study, we performed electrophysiological analyses of synaptic transmission at the medial perforant path (MPP) input onto the GCs in Shn2 knockout mice. While the basal synaptic efficacy was preserved, short-term synaptic depression induced by paired-pulse or low-frequency stimulation was reduced in the mutant mice. High-frequency tetanic stimulation induced lasting synaptic potentiation in both wild-type and mutant mice. However, the decaying synaptic potentiation shortly after the tetanic stimulation was significantly reduced in the mutant mice. These results indicate that the Shn2 deficiency attenuates bidirectional short-term synaptic plasticity at the MPP-GC synapse, thereby rendering the synapse more static. Our finding further supports a possible role of the dentate gyrus dysfunction in pathophysiology of schizophrenia and may also provide important information in interpreting morphology changes of the brain synapses in neuropsychiatric disorders.Electronic supplementary materialThe online version of this article (10.1186/s13041-018-0400-9) contains supplementary material, which is available to authorized users.
机译:海马的齿状回已牵涉到包括精神分裂症在内的神经精神疾病的病理生理基础。我们已经确定了几种在齿状回中具有强大的分子和功能缺陷的神经精神疾病的小鼠模型。其中,已提出缺乏Schnurri-2(Shn2或HIVEP2)的小鼠作为精神分裂症和智力残疾的模型。 Shn2基因敲除小鼠表现出类似精神分裂症和HIVEP2相关智力障碍的行为异常,以及齿状颗粒细胞(GC)的体细胞和输出突触的明显功能改变。尽管在GC中的树突状脊柱形态中也观察到了强烈的异常,但它们的功能相关性仍然未知。在本研究中,我们对Shn2基因敲除小鼠的GC进行了内侧穿孔路径(MPP)输入时突触传递的电生理分析。虽然保留了基础突触功效,但突变小鼠降低了由成对脉冲或低频刺激诱导的短期突触抑制。高频强直性刺激在野生型和突变型小鼠中诱导持久的突触增强。但是,强直刺激后不久,突变小鼠的突触衰减能力明显降低。这些结果表明,Shn2缺乏症削弱了MPP-GC突触的双向短期突触可塑性,从而使突触更加静态。我们的发现进一步支持了齿状回功能障碍在精神分裂症的病理生理中的可能作用,并且还可能为解释神经精神疾病中脑突触的形态变化提供重要信息。电子补充材料本文的在线版本(10.1186 / s13041-018-0400 -9)包含补充材料,授权用户可以使用。

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