首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >From the Cover: Dominant-negative DISC1 transgenic mice display schizophrenia-associated phenotypes detected by measures translatable to humans
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From the Cover: Dominant-negative DISC1 transgenic mice display schizophrenia-associated phenotypes detected by measures translatable to humans

机译:从封面:显性负DISC1转基因小鼠表现出与精神分裂症相关的表型可通过可转化为人类的方法检测

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摘要

Here, we report generation and characterization of Disrupted-In-Schizophrenia-1 (DISC1) genetically engineered mice as a potential model for major mental illnesses, such as schizophrenia. DISC1 is a promising genetic risk factor for major mental illnesses. In this transgenic model, a dominant-negative form of DISC1 (DN-DISC1) is expressed under the αCaMKII promoter. In vivo MRI of the DN-DISC1 mice detected enlarged lateral ventricles particularly on the left side, suggesting a link to the asymmetrical change in anatomy found in brains of patients with schizophrenia. Furthermore, selective reduction in the immunoreactivity of parvalbumin in the cortex, a marker for an interneuron deficit that may underlie cortical asynchrony, is observed in the DN-DISC1 mice. These results suggest that these transgenic mice may be used as a model for schizophrenia. DN-DISC1 mice also display several behavioral abnormalities, including hyperactivity, disturbance in sensorimotor gating and olfactory-associated behavior, and an anhedonia/depression-like deficit.
机译:在这里,我们报告的精神分裂症-1(DISC1)基因工程小鼠的生成和表征作为主要精神疾病,例如精神分裂症的潜在模型。 DISC1是重大精神疾病的有前途的遗传风险因素。在此转基因模型中,DISC1(DN-DISC1)的显性负型表达在αCaMKII启动子下。 DN-DISC1小鼠的体内MRI检测到侧脑室增大,尤其是在左侧,这暗示着精神分裂症患者大脑中解剖结构的不对称变化。此外,在DN-DISC1小鼠中观察到皮层中小白蛋白的免疫反应性选择性降低,皮层中小白蛋白的免疫反应性可能是皮质异步的基础,是神经元间缺乏的标志。这些结果表明,这些转基因小鼠可以用作精神分裂症的模型。 DN-DISC1小鼠还表现出几种行为异常,包括活动过度,感觉运动门控障碍和与嗅觉相关的行为紊乱,以及缺乏快感/抑郁症。

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