Effects of metformin on modulating the expression of brain-related genes of APP/PS1 transgenic mice based on Single Cell Sequencing.

IF 1.8 4区 医学 Q3 CLINICAL NEUROLOGY
Xiao Qiu-Yue, Ye Tian-Yuan, Wang Xiao-Long, Qi Dong-Mei, Cheng Xiao-Rui
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引用次数: 0

Abstract

Background: Alzheimer's disease is the most common form of dementia, affecting millions of people worldwide.

Methods: Here, we analyzed the effects of metformin on APP/PS1 transgenic mice by behavioral test and single-cell sequencing. Results showed that metformin can improve the spatial learning, memory function, and anxiety mood of APP/PS1 transgenic mice. We identified transcriptionally distinct subpopulations of nine major brain cell types. Metformin increased the differentiation of stem cells, decreased the proportion of cells in the G2 phase, enhanced the generation of neural stem cells and oligodendrocyte progenitor cells, and the tendency of neural stem cells to differentiate into astrocytes. Notably, 253 genes expressed abnormally in APP/PS1 transgenic mice and were reversed by metformin. Ttr, Uba52, and Rps21 are the top 3 genes in the cell-gene network with the highest node degree. Moreover, histochemistry showed the expressions of RPS15, UBA52, and RPL23a were consistent with the data from single-cell sequencing. Pathway and biological process enrichment analysis indicated metformin was involved in nervous system development and negative regulation of the apoptotic process.

Conclusion: Overall, metformin might play an important role in the differentiation and development and apoptotic process of the central nervous system by regulating the expression of Ttr, Uba52, Rps21, and other genes to improve cognition of APP/PS1 transgenic mice. These results provided a clue for elaborating on the molecular and cellular basis of metformin on AD.

基于单细胞测序的二甲双胍对APP/PS1转基因小鼠脑相关基因表达的调节作用
背景:阿尔茨海默病是最常见的痴呆症,影响着全球数百万人:方法:本文通过行为测试和单细胞测序分析了二甲双胍对APP/PS1转基因小鼠的影响。结果表明,二甲双胍能改善APP/PS1转基因小鼠的空间学习能力、记忆功能和焦虑情绪。我们在九种主要脑细胞类型中发现了转录不同的亚群。二甲双胍增加了干细胞的分化,降低了G2期细胞的比例,增强了神经干细胞和少突胶质祖细胞的生成,以及神经干细胞向星形胶质细胞分化的趋势。值得注意的是,有253个基因在APP/PS1转基因小鼠体内异常表达,并被二甲双胍逆转。Ttr、Uba52和Rps21是细胞-基因网络中节点度最高的前3个基因。此外,组织化学研究表明,RPS15、UBA52和RPL23a的表达与单细胞测序的数据一致。通路和生物过程富集分析表明,二甲双胍参与了神经系统的发育和凋亡过程的负调控:总之,二甲双胍可能通过调节Ttr、Uba52、Rps21等基因的表达,在中枢神经系统的分化发育和凋亡过程中发挥重要作用,从而改善APP/PS1转基因小鼠的认知能力。这些结果为阐明二甲双胍治疗AD的分子和细胞基础提供了线索。
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来源期刊
Current Alzheimer research
Current Alzheimer research 医学-神经科学
CiteScore
4.00
自引率
4.80%
发文量
64
审稿时长
4-8 weeks
期刊介绍: Current Alzheimer Research publishes peer-reviewed frontier review, research, drug clinical trial studies and letter articles on all areas of Alzheimer’s disease. This multidisciplinary journal will help in understanding the neurobiology, genetics, pathogenesis, and treatment strategies of Alzheimer’s disease. The journal publishes objective reviews written by experts and leaders actively engaged in research using cellular, molecular, and animal models. The journal also covers original articles on recent research in fast emerging areas of molecular diagnostics, brain imaging, drug development and discovery, and clinical aspects of Alzheimer’s disease. Manuscripts are encouraged that relate to the synergistic mechanism of Alzheimer''s disease with other dementia and neurodegenerative disorders. Book reviews, meeting reports and letters-to-the-editor are also published. The journal is essential reading for researchers, educators and physicians with interest in age-related dementia and Alzheimer’s disease. Current Alzheimer Research provides a comprehensive ''bird''s-eye view'' of the current state of Alzheimer''s research for neuroscientists, clinicians, health science planners, granting, caregivers and families of this devastating disease.
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