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作 者:杜小宇 汪澈 郑汝杰 刘旨浩 卢成志[3] DU Xiaoyu;WANG Che;ZHENG Rujie;LIU Zhihao;LU Chengzhi(The First Central Clinical School,Tianjin Medical University,Tianjin 300192,China;Department of Clinical Medicine,School of Medicine,Nankai University,Tianjin 300071,China;Department of Cardiology,Tianjin First Center Hospital,Tianjin 300192,China)
机构地区:[1]天津医科大学一中心临床学院,天津300192 [2]南开大学医学院临床医学系,天津300071 [3]天津市第一中心医院心内科,天津300192
出 处:《天津医科大学学报》2024年第3期224-231,共8页Journal of Tianjin Medical University
基 金:国家自然科学基金(81970303);天津市医学重点学科(专科)建设项目(TJYXZDXK-054B);天津市自然科学基金资助项目(21JCYBJC00250)。
摘 要:目的:通过生物信息学筛选与心肌梗死(MI)后心肌细胞增殖与再生的相关枢纽基因。方法:从GEO数据库下载并合并数据集GSE123863、GSE184792和GSE198300,通过对样本进行加权基因共表达网络分析(WGCNA)筛选枢纽基因。并采用1日龄(增殖组)和7日龄(非增殖组)C57BL/6J乳鼠构建MI模型,每组6只,于术后3 d取MI区组织行实时荧光定量PCR(RT-qPCR)验证枢纽基因的表达情况。结果:通过生物信息学分析共筛选出7个枢纽基因:NDUFB2、CPEB4、TECR、HIC2、IFITM3、ACOT1和ACOT4。动物实验结果显示,与非增殖组相比,在增殖组中NDUFB2、TECR表达显著下降,CPEB4、HIC2、IFITM3和ACOT1表达显著上升(均P<0.05);ACOT4表达呈上升趋势,但无统计学意义(P>0.05)。结论:NDUFB2、CPEB4、TECR、HIC2、IFITM3和ACOT1可能在MI后心肌细胞增殖过程中发挥重要作用。Objective:To screen hub genes associated with cardiomyocyte proliferation after myocardial infarction(MI)by bioinformatics analysis.Methods:Datasets GSE123863,GSE184792,and GSE198300 were downloaded from the GEO database and merged.Weighted gene co-expression network analysis(WGCNA)was performed for samples to screen out the hub genes.Then MI model was constructed using 1-day-old(proliferating group)and 7-day-old(non-proliferating group)C57BL/6J neonatal mice,and 6 mice per group.The MI area was harvested at 3 days postoperatively for real-time quantitative PCR(RT-qPCR)to verify the expression of the hub gene.Results:A total of seven hub genes were screened by bioinformatics analysis:NDUFB2,CPEB4,TECR,HIC2,IFITM3,ACOT1,ACOT4.The results of animal experiments showed that compared with the non-proliferative group,the expression of NDUFB2 and TECR decreased significantly in the proliferative group,while the expression of CPEB4,HIC2,IFITM3,and ACOT1 increased significantly(all P<0.05).Meanwhile,the expression of ACOT4 showed a tendency of increase,but the difference was not statistically significant(P>0.05).Conclusion:NDUFB2,CPEB4,TECR,HIC2,IFITM3,and ACOT1 may play important roles in the proliferation of cardiomyocyte proliferation after MI.
分 类 号:R541.4[医药卫生—心血管疾病]
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