首页|骨关节炎过程中葡萄糖代谢基因的筛选与验证

骨关节炎过程中葡萄糖代谢基因的筛选与验证

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背景:葡萄糖代谢过程在维持机体正常生理功能中扮演着至关重要的角色,当葡萄糖代谢出现紊乱时,可能会导致一系列的健康问题.目前,骨关节炎中葡萄糖代谢相关分子机制和潜在基因靶点有待进一步研究.目的:通过生物信息学方法分析骨关节炎中葡萄糖代谢相关基因,并利用体外细胞实验加以验证,以期为葡萄糖代谢角度防治骨关节炎提供新的思路.方法:使用GEO数据库和GeneCards数据库筛选出骨关节炎差异表达基因和葡萄糖代谢相关基因,两者取交集,得到骨关节炎和葡萄糖代谢共同相关的基因集合,采用GO和KEGG富集分析筛选这些基因的功能和通路.为了进一步研究这些基因之间的相互作用,构建蛋白-蛋白互作网络,并利用Cytoscape软件的计算方法来识别骨关节炎葡萄糖代谢的关键基因(Hub基因).此外,采用CIBERSORT算法对GSE98918数据集免疫细胞浸润分析.最后通过体外细胞实验验证Hub基因的表达情况.结果与结论:①共获得134个骨关节炎葡萄糖代谢相关基因.②GO富集分析表明其主要参与对有毒物质的反应、炎症反应的正调节、对脂多糖的反应等过程.③KEGG富集分析表明其与PI3K-Akt信号通路、白细胞介素17信号通路、糖尿病并发症中的AGE-RAGE信号通路密切相关.④免疫浸润分析得到的主要免疫浸润细胞为巨噬细胞、单核细胞、静息状态下的NK细胞、调节性T细胞、CD8+T细胞.⑤体外细胞实验结果显示:相比于对照组,实验组中Hub基因SERPINF1、TAC1、GLUL、APOE、TMEM176A表达具有显著差异,HLA-DRA的mRNA表达没有统计学意义.结果显示:SERPINF1、TAC1、GLUL、APOE、TMEM176A可作为骨关节炎葡萄糖代谢的关键基因,有望成为防治骨关节炎的新靶点.
Screening and validation of glucose metabolism genes in osteoarthritis
BACKGROUND:Glucose metabolism plays a crucial role in maintaining the normal physiological function of the body.Glucose metabolism disorder can lead to a range of health problems.At present,the molecular mechanism of glucose metabolism and potential gene targets in osteoarthritis need to be further studied.OBJECTIVE:To analyze the genes related to glucose metabolism in osteoarthritis by bioinformatics methods,and to verify them by cell experiments in vitro,so as to provide new ideas for prevention and treatment of osteoarthritis from the perspective of glucose metabolism.METHODS:Differentially expressed genes and glucose metabolism related genes were screened out from GEO database and GeneCards database.The genes related to both osteoarthritis and glucose metabolism were obtained.Gene Ontology(GO)and Kyoto Encyclopedia of Genes and Genomes(KEGG)enrichment analysis were used to screen the functions and pathways of these genes.To further investigate the interactions between these genes,a protein-protein interaction network was constructed and computational methods using Cytoscape software were utilized to identify key genes(Hub genes)for osteoarthritis glucose metabolism.In addition,CIBERSORT algorithm was used to analyze immune cell infiltration in GSE98918 data set.Finally,the expression of Hub gene was verified by cell experiment in vitro.RESULTS AND CONCLUSION:A total of 134 osteoarthritis glucose metabolism-related genes were obtained.GO enrichment analysis showed that GO was mainly involved in the reaction of toxic substances,the positive regulation of inflammatory reaction,the reaction of lipopolysaccharide and so on.KEGG enrichment analysis showed that it was closely related to PI3K-Akt signaling pathway,interleukin-17 signaling pathway,and AGE-RAGE signaling pathway in diabetic complications.Macrophages,monocytes,resting natural killer cells,regulatory T cells,and CD8+T cells were the main infiltrating cells obtained by immune infiltration analysis.In vitro cell experiments showed that the expression of Hub genes SERPINF1,TAC1,GLUL,APOE,and TMEM176A in the experimental group was significantly different from that in the control group.The mRNA expression of HLA-DRA was not statistically significant.The results show that SERPINF1,TAC1,Glul,APOE,and TMEM176A may be the key genes of glucose metabolism in osteoarthritis,and may be potential new targets for the prevention and treatment of osteoarthritis.

osteoarthritisglucose metabolismbioinformaticsdifferentially expressed genesPPI networkimmune infiltrationenrichment analysisengineered tissue construction

柳可心、马超、刘凯、郝茂辰、王杏如、孟令婷、冬梅、王建忠

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内蒙古医科大学,内蒙古自治区呼和浩特市 010030

内蒙古医科大学第二附属医院 创伤外科中心C区,,内蒙古自治区呼和浩特市 010030

内蒙古医科大学第二附属医院,骨质疏松科,内蒙古自治区呼和浩特市 010030

骨关节炎 葡萄糖代谢 生物信息学 差异表达基因 PPI网络 免疫浸润 富集分析 工程化组织构建

2025

中国组织工程研究
中国康复医学会,《中国组织工程研究与临床康复》杂志社

中国组织工程研究

北大核心
影响因子:1.387
ISSN:2095-4344
年,卷(期):2025.29(20)