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作 者:林梅英 甘东辉 高颖 王正杰 陈志敏 LIN Meiying;GAN Donghui;GAO Ying;WANG Zhengjie;CHEN Zhimin(Affiliated Hospital of Putian College, Putian 351100, China)
出 处:《医学研究与教育》2022年第1期8-14,共7页Medical Research and Education
基 金:莆田学院校内科研项目(2019040,2019044)。
摘 要:目的通过生物信息学方法筛选原发性抗磷脂综合征(antiphospholipid syndrome,APS)患者中性粒细胞中的关键差异基因,并鉴定其参与的生物功能和信号通路。方法在GEO数据库中下载APS患者中性粒细胞的RNA测序数据,使用R语言中的limma包筛选差异表达基因,通过clusterProfiler包分别对上调和下调基因进行基因本体论(gene ontology,GO)和京都基因与基因组百科全书(Kyoto encyclopedia of genes and genomes,KEGG)富集分析。最后,通过STRING数据库构建蛋白-蛋白互作网络,使用Cytoscape软件计算网络中的核心基因。结果共筛选得到512个上调基因,473个下调基因,上调基因主要参与的功能和通路包括固有免疫反应调节、中性粒细胞激活、炎症复合体形成等,下调基因主要参与的功能和通路包括T细胞激活、淋巴细胞分化、淋巴细胞激活等。IFIT1、IFI35、IFI3、CCL2、TLR8、FCGR1A是核心的上调基因。MYC、CD8A、FYN、CD28、LCK、GNB2L1是核心的下调基因。结论通过生物信息学方法分析出的核心基因可能是APS患者中性粒细胞发挥免疫效应的关键靶点。Objective To screen key differential genes and identify the biological functions and signaling pathways involved in neutrophils from patients with primary antiphospholipid syndrome(APS)by bioinformatic methods.Methods RNA sequencing data of neutrophils from APS patients were downloaded from the GEO database,differentially expressed genes were screened by using the limma package in R language,and up-and down-regulated genes were subjected to gene ontology(GO)and Kyoto Encyclopedia of Genes and Genomes(KEGG)enrichment analysis by clusterProfiler,respectively.Finally,protein-protein interaction network was constructed by STRING database and core genes in the network were calculated using cytoscape software.Results A total of 512 up-regulated genes and 473 down-regulated genes were obtained by limma package screening.Up-regulated geneswere mainly involved in functions and pathways including regulation of innate immune response,neutrophil activation,inflammatory complex formation,etc.down-regulated genes were mainly involvedin functions and pathways including T cell activation,lymphocyte differentiation,lymphocyte activation,etc.IFIT1,IFI35,IFI3,CCL2,TLR8,FCGR1A were the core genes among the up-regulated genes.MYC,CD8A,FYN,CD28,LCK,GNB2L1 were the core genes among the down-regulated genes.Conclusion The core genes identified by bioinformatic methods may be the key targets for the immune effects of neutrophils in patients with primary antiphospholipid syndrome.
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