Suppr超能文献

FVB品系成年雄性FMR1基因敲除小鼠的脑区体积变化

Regional brain volumes changes in adult male FMR1-KO mouse on the FVB strain.

作者信息

Lai J K Y, Lerch J P, Doering L C, Foster J A, Ellegood J

机构信息

Department of Psychiatry and Behavioural Neuroscience, McMaster University, Brain-Body Institute, St. Joseph's Healthcare, 50 Charlton Avenue East, Hamilton, Ontario L8N 4A6, Canada.

Department of Medical Biophysics, University of Toronto, Mouse Imaging Centre, Hospital for Sick Children, 25 Orde Street, Toronto, Ontario M5T 3H7, Canada.

出版信息

Neuroscience. 2016 Mar 24;318:12-21. doi: 10.1016/j.neuroscience.2016.01.021. Epub 2016 Jan 12.

Abstract

Fragile X Syndrome (FXS) is the most common heritable single gene cause of autism spectrum disorder (ASD). FMR1-KO mice mimic the etiology and phenotypic manifestations of FXS. Neuroanatomical changes in specific brain regions have been reported in clinical settings and in preclinical models. FMR1-KO mice have been generated in different strains including C57Bl/6 (B6) and FVB. Mice on different genetic backgrounds have stable yet distinct behavioral phenotypes that may lead to unique gene-strain interactions on brain structure. Previous magnetic resonance imaging (MRI) studies have examined FMR1 knockout male mice on a B6 and found few differences compared to wild-type mice. Here, we examine brain volumes in FMR1 knockout male mice on a FVB background using high resolution (multi-channel 7.0Tesla) MRI. We observe multiple differences in the neuroanatomy of male FMR1-/y mice on a FVB background. Significantly larger relative volume (% total brain volume) differences were found in major white matter structures throughout the brain. In addition, there were changes in areas associated with fronto-striatal circuitry and other regions. Functional and structural connectivity differences are often seen in human ASD, and therefore, this increased white matter seen in the FMR1-KO-FVB could be highlighting a structural over-connectivity, which could lead to some of the behavioral abnormalities seen with the FMR1-KO-FVB mice. Furthermore, these results highlight the importance of genetic strain contribution to brain structure.

摘要

脆性X综合征(FXS)是自闭症谱系障碍(ASD)最常见的遗传性单基因病因。FMR1基因敲除小鼠模拟了FXS的病因和表型表现。临床环境和临床前模型中均已报道了特定脑区的神经解剖学变化。FMR1基因敲除小鼠已在包括C57Bl/6(B6)和FVB在内的不同品系中培育出来。具有不同遗传背景的小鼠具有稳定但不同的行为表型,这可能导致在脑结构上出现独特的基因-品系相互作用。先前的磁共振成像(MRI)研究检查了B6品系的FMR1基因敲除雄性小鼠,发现与野生型小鼠相比差异不大。在此,我们使用高分辨率(多通道7.0特斯拉)MRI检查了FVB背景下FMR1基因敲除雄性小鼠的脑容量。我们观察到FVB背景下雄性FMR1-/y小鼠的神经解剖学存在多种差异。在整个大脑的主要白质结构中发现了显著更大的相对体积(占全脑体积的百分比)差异。此外,与额纹状体回路和其他区域相关的区域也有变化。在人类ASD中经常可以看到功能和结构连接性的差异,因此,在FMR1-KO-FVB小鼠中观察到的白质增加可能突出了一种结构上的过度连接,这可能导致FMR1-KO-FVB小鼠出现一些行为异常。此外,这些结果突出了遗传品系对脑结构的重要贡献。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验