在精神分裂症小鼠模型中,与c -激酶1 (PICK1)相互作用的蛋白调节突触功能和逆转学习。

IF 6.6 1区 医学 Q1 NEUROSCIENCES
James N Samsom, MengYi Xu, Ariel Ávila, Anastasios A Daskalakis, Jia Hong Dai, Xing Gao, John Georgiou, Graham L Collingridge, Fang Liu, Albert H C Wong
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引用次数: 0

摘要

与c -激酶1 (PICK1)相互作用的蛋白质通过指导谷氨酸受体和其他蛋白质的运输对突触可塑性至关重要。PICK1基因变异与精神分裂症有关。为了研究PICK1在精神分裂症相关行为中的作用,研究人员对PICK1脂质相互作用BAR结构域突变的小鼠进行了表征。雄性Pick1-S262T小鼠海马和前额皮质(PFC) AMPA受体(AMPAR)亚基GluA1和GluA2蛋白表达被破坏。Pick1-S262T小鼠显示海马突触传递减少和长期抑郁(LTD)缺陷,而非幼年(P21)。突变雄性在Morris水迷宫(MWM)中也存在逆向学习缺陷。这些观察结果表明,Pick1-S262T突变影响AMPAR运输,破坏突触传递和可塑性,以及认知灵活性,这是精神分裂症的核心神经心理缺陷。这项工作提出了可能的机制,通过已知的精神分裂症易感基因可能有助于该疾病的临床特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Protein interacting with C-kinase 1 (PICK1) regulates synaptic function and reversal learning in a mouse model for schizophrenia.

Protein interacting with C-kinase 1 (PICK1) is important for synaptic plasticity through directing transport of glutamate receptors and other proteins. PICK1 gene variants have been associated with schizophrenia. To examine the role of PICK1 in schizophrenia-related behaviors, mice with a mutation in the PICK1 lipid-interacting BAR domain were characterized. Male Pick1-S262T mice had disrupted AMPA receptor (AMPAR) subunit GluA1 and GluA2 protein expression in the hippocampus and prefrontal cortex (PFC). Young adult, but not juvenile (P21), Pick1-S262T mice showed decreased hippocampal synaptic transmission and deficits in long-term depression (LTD). Mutant males also had deficits in reversal learning in the Morris water maze (MWM). These observations suggest that the Pick1-S262T mutation affects AMPAR trafficking, disrupting synaptic transmission and plasticity, as well as cognitive flexibility, a core neuropsychological deficit in schizophrenia. This work suggests possible mechanisms by which a known schizophrenia susceptibility gene could contribute to clinical features of the disorder.

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来源期刊
Neuropsychopharmacology
Neuropsychopharmacology 医学-精神病学
CiteScore
15.00
自引率
2.60%
发文量
240
审稿时长
2 months
期刊介绍: Neuropsychopharmacology is a reputable international scientific journal that serves as the official publication of the American College of Neuropsychopharmacology (ACNP). The journal's primary focus is on research that enhances our knowledge of the brain and behavior, with a particular emphasis on the molecular, cellular, physiological, and psychological aspects of substances that affect the central nervous system (CNS). It also aims to identify new molecular targets for the development of future drugs. The journal prioritizes original research reports, but it also welcomes mini-reviews and perspectives, which are often solicited by the editorial office. These types of articles provide valuable insights and syntheses of current research trends and future directions in the field of neuroscience and pharmacology.
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