Comparison of Cerebral Cortex Transcriptome Profiles in Ischemic Stroke and Alzheimer's Disease Models.

Clinical nutrition research Pub Date : 2022-07-25 eCollection Date: 2022-07-01 DOI:10.7762/cnr.2022.11.3.159
Juhyun Song
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引用次数: 1

Abstract

Ischemic stroke and Alzheimer's disease (AD) are representative geriatric diseases with a rapidly increasing prevalence worldwide. Recent studies have reported an association between ischemic stroke neuropathology and AD neuropathology. Ischemic stroke shares some similar characteristics with AD, such as glia activation-induced neuroinflammation, amyloid beta accumulation, and neuronal cell loss, as well as some common risk factors with AD progression. Although there are considerable similarities in neuropathology between ischemic stroke and AD, no studies have ever compared specific genetic changes of brain cortex between ischemic stroke and AD. Therefore, in this study, I compared the cerebral cortex transcriptome profile of 5xFAD mice, an AD mouse model, with those of middle cerebral artery occlusion (MCAO) mice, an ischemic stroke mouse model. The data showed that the expression of many genes with important functional implications in MCAO mouse brain cortex were related to synaptic dysfunction and neuronal cell death in 5xFAD mouse model. In addition, changes in various protein-coding RNAs involved in synaptic plasticity, amyloid beta accumulation, neurogenesis, neuronal differentiation, glial activation, inflammation and neurite outgrowth were observed. The findings could serve as an important basis for further studies to elucidate the pathophysiology of AD in patients with ischemic stroke.

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缺血性卒中和阿尔茨海默病模型中大脑皮层转录组谱的比较
缺血性脑卒中和阿尔茨海默病(AD)是具有代表性的老年疾病,在世界范围内的患病率迅速上升。最近的研究报道了缺血性卒中神经病理与AD神经病理之间的关联。缺血性卒中与AD有一些相似的特征,如胶质细胞激活诱导的神经炎症、淀粉样蛋白积累和神经元细胞损失,以及AD进展的一些共同危险因素。尽管缺血性卒中和AD在神经病理学上有相当多的相似之处,但尚未有研究比较缺血性卒中和AD之间大脑皮层的特定遗传变化。因此,在本研究中,我比较了5xFAD小鼠(AD小鼠模型)与大脑中动脉闭塞(MCAO)小鼠(缺血性卒中小鼠模型)的大脑皮层转录组谱。数据显示,MCAO小鼠脑皮层中许多具有重要功能意义的基因的表达与5xFAD小鼠突触功能障碍和神经元细胞死亡有关。此外,我们还观察了参与突触可塑性、β淀粉样蛋白积累、神经发生、神经元分化、胶质活化、炎症和神经突生长的各种蛋白质编码rna的变化。本研究结果可为进一步研究缺血性脑卒中患者AD的病理生理机制提供重要依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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