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Age-Associated mRNA and miRNA Expression Changes in the Blood-Brain Barrier

机译:年龄相关的mRNA和miRNA在血脑屏障中的表达变化。

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Functional and structural age-associated changes in the blood-brain barrier (BBB) may affect the neurovascular unit and contribute to the onset and progression of age-associated neurodegenerative pathologies, including Alzheimer’s disease. The current study interrogated the RNA profile of the BBB in an ageing human autopsy brain cohort and an ageing mouse model using combined laser capture microdissection and expression profiling. Only 12 overlapping genes were altered in the same direction in the BBB of both ageing human and mouse cohorts. These included genes with roles in regulating vascular tone, tight junction protein expression and cell adhesion, all processes prone to dysregulation with advancing age. Integrated mRNA and miRNA network and pathway enrichment analysis of the datasets identified 15 overlapping miRNAs that showed altered expression. In addition to targeting genes related to DNA binding and/or autophagy, many of the miRNAs identified play a role in age-relevant processes, including BBB dysfunction and regulating the neuroinflammatory response. Future studies have the potential to develop targeted therapeutic approaches against these candidates to prevent vascular dysfunction in the ageing brain.
机译:血脑屏障(BBB)的功能和结构与年龄相关的变化可能会影响神经血管单位,并导致与年龄相关的神经退行性病变(包括阿尔茨海默氏病)的发作和进展。当前的研究使用结合的激光捕获显微切割和表达谱分析,在衰老的人类尸体解剖脑群和衰老的小鼠模型中询问了BBB的RNA谱。在人类和小鼠老龄群体的血脑屏障中,只有12个重叠基因沿相同方向改变。这些基因包括在调节血管紧张度,紧密连接蛋白表达和细胞粘附中起作用的基因,所有过程都随着年龄的增长易于失调。集成的mRNA和miRNA网络以及对数据集的途径富集分析确定了15个重叠的miRNA,这些miRNA显示出表达改变。除了靶向与DNA结合和/或自噬相关的基因外,鉴定出的许多miRNA在与年龄相关的过程中也起作用,包括BBB功能障碍和调节神经炎症反应。未来的研究有可能针对这些候选药物开发靶向治疗方法,以预防衰老的大脑中的血管功能障碍。

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