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首页> 外文期刊>Frontiers in Genetics >Identification of Pre-symptomatic Gene Signatures That Predict Resilience to Cognitive Decline in the Genetically Diverse AD-BXD Model
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Identification of Pre-symptomatic Gene Signatures That Predict Resilience to Cognitive Decline in the Genetically Diverse AD-BXD Model

机译:预测在遗传多样的AD-BXD模型中对认知能力下降的适应能力的症状前基因特征的识别

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摘要

Across the population, individuals exhibit a wide variation of susceptibility or resilience to developing Alzheimer’s disease (AD). Identifying specific factors that promote resilience would provide insight into disease mechanisms and nominate potential targets for therapeutic intervention. Here, we use transcriptome profiling to identify gene networks present in the pre-symptomatic AD mouse brain relating to neuroinflammation, brain vasculature, extracellular matrix organization, and synaptic signaling that predict cognitive performance at an advanced age. We highlight putative drivers of these observed relationships, including Itgb2 , Fcgr2b, Slc6a14 , and Gper1 , which represent prime targets through which to promote resilience prior to overt symptom onset. In addition, we identify a genomic region on chromosome 2 containing variants that directly modulate resilience network expression. Overall, work here highlights new potential drivers of resilience to AD and contributes significantly to our understanding of early, potentially causal, disease mechanisms.
机译:在整个人群中,个体对发展为阿尔茨海默氏病(AD)的敏感性或适应力差异很大。确定促进弹性的特定因素将提供对疾病机制的了解,并指定治疗干预的潜在目标。在这里,我们使用转录组分析来识别症状前AD小鼠大脑中存在的基因网络,这些网络与神经发炎,脑血管系统,细胞外基质组织和突触信号有关,可预测高龄患者的认知表现。我们重点介绍这些观察到的关系的推定驱动因素,包括Itgb2,Fcgr2b,Slc6a14和Gper1,它们代表主要的靶标,通过这些靶标,可以在症状发作之前增强适应力。此外,我们在2号染色体上鉴定了一个基因组区域,其中包含直接调节弹性网络表达的变体。总的来说,这里的工作突出了新的抗AD潜在驱动力,并为我们对早期潜在病因机制的理解做出了重要贡献。

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