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慢性阻塞性肺疾病(COPD)肺泡巨噬细胞中差异表达基因的生物信息学分析

[Bioinformatical analysis of differentially expressed genes in alveolar macrophages of chronic obstructive pulmonary disease(COPD)].

作者信息

Wang Xiaole, Zhu Jie, Tong Jiabing, Wu Fan, Gao Yating, Wang Xinheng, Li Zegeng

机构信息

Graduate School, Anhui University of Chinese Medicine, Hefei 230012, China.

Institute of Medicine for Respiratory Diseases, Anhui Academy of Chinese Medicine, Hefei 230031, China.

出版信息

Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2020 Nov;36(11):961-966.

Abstract

Objective To analyze the differentially expressed genes (DEGs) in alveolar macrophages (AMs) of patients with chronic obstructive pulmonary disease (COPD) and their potential roles in the pathogeneses of COPD using bioinformatics. Methods Gene chip and RNA sequencing data sets of AMs in patients with COPD were downloaded from GEO. Limma and Degseq2 packages in R software were applied to obtain DEGs, and the GO enrichment analysis, the Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis, protein-protein interaction analysis (PPI), and the hub gene analysis were performed to predict the molecular mechanisms of DEGs. Results Through the integration of three data sets, a total of 43 DEGs of AMs were obtained, and the function predictive analysis found that the 43 DEGs were primarily related to chemokines, cytokines, complement, cytochrome P450, etc., which mainly included the significantly low expression of C-X-C motif chemokine ligand 9 (CXCL9), CXCL11, etc. and the significantly high expression of cytochrome P450 family 1 subfamily B member 1 (CYP1B1). Conclusion The DEGs of AMs in patients with COPD are related to the molecular mechanisms of immunity and inflammation and might be involved in the pathogenesis of chronic inflammation of COPD.

摘要

目的 运用生物信息学分析慢性阻塞性肺疾病(COPD)患者肺泡巨噬细胞(AMs)中差异表达基因(DEGs)及其在COPD发病机制中的潜在作用。方法 从基因表达综合数据库(GEO)下载COPD患者AMs的基因芯片和RNA测序数据集。应用R软件中的Limma和Degseq2软件包获取DEGs,并进行基因本体(GO)富集分析、京都基因与基因组百科全书(KEGG)富集分析、蛋白质-蛋白质相互作用分析(PPI)以及枢纽基因分析,以预测DEGs的分子机制。结果 通过整合三个数据集,共获得43个AMs的DEGs,功能预测分析发现这43个DEGs主要与趋化因子、细胞因子、补体、细胞色素P450等相关,其中主要包括C-X-C基序趋化因子配体9(CXCL9)、CXCL11等显著低表达,以及细胞色素P450家族1亚家族B成员1(CYP1B1)显著高表达。结论 COPD患者AMs的DEGs与免疫和炎症的分子机制相关,可能参与COPD慢性炎症的发病机制。

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