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Immature morphological properties in subcellular-scale structures in the dentate gyrus of Schnurri-2 knockout mice: a model for schizophrenia and intellectual disability

机译:Schnurri-2基因敲除小鼠的齿状回亚细胞规模结构中的未成熟形态学特性:精神分裂症和智力残疾的模型

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摘要

Accumulating evidence suggests that subcellular-scale structures such as dendritic spine and mitochondria may be involved in the pathogenesis/pathophysiology of schizophrenia and intellectual disability. Previously, we proposed mice lacking Schnurri-2 (Shn2; also called major histocompatibility complex [MHC]-binding protein 2 [MBP-2], or human immunodeficiency virus type I enhancer binding protein 2 [HIVEP2]) as a schizophrenia and intellectual disability model with mild chronic inflammation. In the mutants’ brains, there are increases in C4b and C1q genes, which are considered to mediate synapse elimination during postnatal development. However, morphological properties of subcellular-scale structures such as dendritic spine in Shn2 knockout (KO) mice remain unknown. In this study, we conducted three-dimensional morphological analyses in subcellular-scale structures in dentate gyrus granule cells of Shn2 KO mice by serial block-face scanning electron microscopy. Shn2 KO mice showed immature dendritic spine morphology characterized by increases in spine length and decreases in spine diameter. There was a non-significant tendency toward decrease in spine density of Shn2 KO mice over wild-type mice, and spine volume was indistinguishable between genotypes. Shn2 KO mice exhibited a significant reduction in GluR1 expression and a nominally significant decrease in SV2 expression, while PSD95 expression had a non-significant tendency to decrease in Shn2 KO mice. There were significant decreases in dendrite diameter, nuclear volume, and the number of constricted mitochondria in the mutants. Additionally, neuronal density was elevated in Shn2 KO mice. These results suggest that Shn2 KO mice serve as a unique tool for investigating morphological abnormalities of subcellular-scale structures in schizophrenia, intellectual disability, and its related disorders.Electronic supplementary materialThe online version of this article (10.1186/s13041-017-0339-2) contains supplementary material, which is available to authorized users.
机译:越来越多的证据表明,亚细胞规模的结构(例如树突棘和线粒体)可能与精神分裂症的发病机制/病理生理和智力残疾有关。以前,我们提出了缺乏Schnurri-2(Shn2;也称为主要组织相容性复合物[MHC]-结合蛋白2 [MBP-2]或人类免疫缺陷病毒I型增强子结合蛋白2 [HIVEP2])的小鼠作为精神分裂症和智力障碍慢性炎症的模型。在突变体的大脑中,C4b和C1q基因增加,被认为在产后发育过程中介导突触消除。但是,Sn2基因敲除(KO)小鼠亚细胞规模的结构,如树突棘的形态学特性仍然未知。在这项研究中,我们通过串行块面扫描电子显微镜对Shn2 KO小鼠的齿状回颗粒细胞的亚细胞尺度结构进行了三维形态分析。 Shn2 KO小鼠表现出不成熟的树突状脊柱形态,其特征在于脊柱长度增加和脊柱直径减小。与野生型小鼠相比,Shn2 KO小鼠的脊柱密度没有明显降低的趋势,并且基因型之间的脊柱体积没有区别。 Shn2 KO小鼠表现出GluR1表达的显着减少和SV2表达的名义上显着的减少,而PSD95表达在Shn2 KO小鼠中没有明显的下降趋势。突变体中的枝晶直径,核体积和线粒体收缩数目显着减少。此外,Shn2 KO小鼠神经元密度升高。这些结果表明Shn2 KO小鼠是研究精神分裂症,智力障碍及其相关疾病的亚细胞尺度结构形态异常的独特工具。电子补充材料本文的在线版本(10.1186 / s13041-017-0339-2 )包含补充材料,授权用户可以使用。

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