Suppr超能文献

环氧化酶敲除小鼠基因表达的微阵列分析 - 与自闭症谱系障碍的关联。

Microarray analysis of gene expression in the cyclooxygenase knockout mice - a connection to autism spectrum disorder.

机构信息

Neuroscience Graduate Diploma Program, York University, Toronto, ON, M3J 1P3, Canada.

Department of Biology, York University, Toronto, ON, Canada.

出版信息

Eur J Neurosci. 2018 Mar;47(6):750-766. doi: 10.1111/ejn.13781. Epub 2017 Dec 15.

Abstract

The cellular and molecular events that take place during brain development play an important role in governing function of the mature brain. Lipid-signalling molecules such as prostaglandin E (PGE ) play an important role in healthy brain development. Abnormalities along the COX-PGE signalling pathway due to genetic or environmental causes have been linked to autism spectrum disorder (ASD). This study aims to evaluate the effect of altered COX-PGE signalling on development and function of the prenatal brain using male mice lacking cyclooxygenase-1 and cyclooxygenase-2 (COX-1 and COX-2 ) as potential model systems of ASD. Microarray analysis was used to determine global changes in gene expression during embryonic days 16 (E16) and 19 (E19). Gene Ontology: Biological Process (GO:BP) and Kyoto Encyclopedia of Genes and Genomes (KEGG) were implemented to identify affected developmental genes and cellular processes. We found that in both knockouts the brain at E16 had nearly twice as many differentially expressed genes, and affected biological pathways containing various ASD-associated genes important in neuronal function. Interestingly, using GeneMANIA and Cytoscape we also show that the ASD-risk genes identified in both COX-1 and COX-2 models belong to protein-interaction networks important for brain development despite of different cellular localization of these enzymes. Lastly, we identified eight genes that belong to the Wnt signalling pathways exclusively in the COX-2 mice at E16. The level of PKA-phosphorylated β-catenin (S552), a major activator of the Wnt pathway, was increased in this model, suggesting crosstalk between the COX-2-PGE and Wnt pathways during early brain development. Overall, these results provide further molecular insight into the contribution of the COX-PGE pathways to ASD and demonstrate that COX-1 and COX-2 animals might be suitable new model systems for studying the disorders.

摘要

在大脑发育过程中发生的细胞和分子事件对成熟大脑的功能起着重要作用。脂质信号分子,如前列腺素 E (PGE),在健康的大脑发育中起着重要作用。由于遗传或环境原因导致 COX-PGE 信号通路异常与自闭症谱系障碍 (ASD) 有关。本研究旨在使用缺乏环氧化酶-1 和环氧化酶-2 (COX-1 和 COX-2) 的雄性小鼠评估改变的 COX-PGE 信号对产前大脑发育和功能的影响,作为 ASD 的潜在模型系统。微阵列分析用于确定胚胎第 16 天 (E16) 和第 19 天 (E19) 期间基因表达的全局变化。基因本体论:生物过程 (GO:BP) 和京都基因与基因组百科全书 (KEGG) 用于识别受影响的发育基因和细胞过程。我们发现,在两种敲除小鼠中,E16 时的大脑有近两倍的差异表达基因,并且受影响的生物途径包含各种与神经元功能相关的 ASD 相关基因。有趣的是,使用 GeneMANIA 和 Cytoscape,我们还表明,在 COX-1 和 COX-2 模型中鉴定的 ASD 风险基因属于蛋白质相互作用网络,这些网络对大脑发育很重要,尽管这些酶的细胞定位不同。最后,我们在 E16 时的 COX-2 小鼠中仅鉴定出属于 Wnt 信号通路的 8 个基因。Wnt 通路的主要激活剂 PKA 磷酸化 β-连环蛋白 (S552) 的水平在该模型中增加,表明 COX-2-PGE 和 Wnt 通路在早期大脑发育过程中存在串扰。总的来说,这些结果为 COX-PGE 途径对 ASD 的贡献提供了进一步的分子见解,并表明 COX-1 和 COX-2 动物可能是研究这些疾病的合适新模型系统。

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