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先天自闭症模型中小狨猴新生幼崽的异常轴突导向信号和前连合减少的半球间连接。

Abnormal axon guidance signals and reduced interhemispheric connection via anterior commissure in neonates of marmoset ASD model.

机构信息

Department of Ultrastructural Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry, 4-1-1 Ogawa-Higashi, Kodaira, Tokyo, 187-8502, Japan; Department of Functional Brain Imaging, National Institute of Radiological Sciences, National Institutes for Quantum and Radiological Science and Technology (QST), 4-9-1 Anagawa, Inage-ku, Chiba, Chiba, 263-8555, Japan.

Department of Ultrastructural Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry, 4-1-1 Ogawa-Higashi, Kodaira, Tokyo, 187-8502, Japan.

出版信息

Neuroimage. 2019 Jul 15;195:243-251. doi: 10.1016/j.neuroimage.2019.04.006. Epub 2019 Apr 3.

Abstract

In autism spectrum disorder (ASD), disrupted functional and structural connectivity in the social brain has been suggested as the core biological mechanism underlying the social recognition deficits of this neurodevelopmental disorder. In this study, we aimed to identify genetic and neurostructural abnormalities at birth in a non-human primate model of ASD, the common marmoset with maternal exposure to valproic acid (VPA), which has been reported to display social recognition deficit in adulthood. Using a comprehensive gene expression analysis, we found that 20 genes were significantly downregulated in VPA-exposed neonates. Of these, Frizzled3 (FZD3) and PIK3CA were identified in an axon guidance signaling pathway. FZD3 is essential for the normal development of the anterior commissure (AC) and corpus callosum (CC); hence, we performed diffusion tensor magnetic resonance imaging with a 7-Tesla scanner to measure the midsagittal sizes of these structures. We found that the AC size in VPA-exposed neonates was significantly smaller than that in age-matched controls, while the CC size did not differ. These results suggest that downregulation of the genes related to axon guidance and decreased AC size in neonatal primates may be linked to social brain dysfunctions that can happen later in life.

摘要

在自闭症谱系障碍 (ASD) 中,社交大脑中功能和结构连接的中断被认为是这种神经发育障碍社交识别缺陷的核心生物学机制。在这项研究中,我们旨在在 ASD 的非人类灵长类动物模型(即接受丙戊酸 (VPA) 暴露的普通狨猴)中,确定出生时的遗传和神经结构异常,该模型已被报道在成年后表现出社交识别缺陷。使用全面的基因表达分析,我们发现 20 个基因在 VPA 暴露的新生儿中显著下调。其中,Frizzled3 (FZD3) 和 PIK3CA 被确定在轴突导向信号通路中。FZD3 对于前连合 (AC) 和胼胝体 (CC) 的正常发育至关重要;因此,我们使用 7 特斯拉扫描仪进行弥散张量磁共振成像,以测量这些结构的正中矢状面大小。我们发现 VPA 暴露的新生儿的 AC 大小明显小于年龄匹配的对照组,而 CC 大小没有差异。这些结果表明,与轴突导向相关的基因下调以及新生灵长类动物的 AC 大小减小,可能与以后生活中发生的社交大脑功能障碍有关。

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