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作 者:王玉浔[1] 姜埃利[1] Wang Yuxun;Jiang Aili(Blood Purification Center,the Second Hospital of Tianjin Medical University,Tianjing 300201,China)
出 处:《中华实验外科杂志》2018年第11期2089-2091,共3页Chinese Journal of Experimental Surgery
摘 要:目的应用高通量长链非编码RNA(1ncRNA)芯片检测小鼠腹膜纤维化组织与正常小鼠腹膜组织中lncRNAs表达的差异,探讨lncRNAs与腹膜纤维化的关系。方法将30只C57BL/6雄性小鼠随机分为正常组、4周模型组、6周模型组;模型组给予腹腔灌注4.5%腹膜透析液(广州百特公司)。分别于实验4周和6周后提取小鼠脏层腹膜组织的RNA,进行差异lncRNAs的筛选,用反转录-聚合酶链反应(RT-PCR)法验证差异表达的lncRNAs。结果芯片结果显示2倍以上变化且差异有统计学意义的lncRNAs共有857条。其中,随着纤维化时间的延长,呈显著上调的有186条;显著下调的有231条(P〈0.05)。结论在小鼠腹膜纤维化组织中lncRNAs的表达谱发生了动态变化,且差异显著,提示lncRNAs可能参与了腹膜纤维化发生发展的基因调控。Objective To detect the dynamic expression of long non-coding RNA (lncRNA) in normal and peritoneal fibrosis tissue using microarray, and to discuss the relationship between lncRNA and peritoneal fibrosis. Methods Thirty male C57BL/6 mice were divided into three groups: normal group, model group for 4 weeks,model group for 6 weeks. Two model groups were injected with 4. 5% peritoneal dialysis fluid (Baxter). RNA was extracted from mice's visceral peritoneal tissue at 4 and 6 weeks after the experiment; Then the lncRNAs expression levels were detected by mieroarray in normal group and model groups separately; Finally the differentially expressed lncRNAs were identified by reverse transcriptase-polymerase chain reaction (RT-PCR). Results There were 857 lncRNAs differentially expressed more than 2 times in peritoneal fibrosis tissue as compared with nomal peritoneal tissue. Among them, with the prolongation of fibrosis time, 186 lncRNAs were significantly up-regulated, and 231 lneRNAs were significant down-regulated (P〈0.05). Conclusion The expression profile of lncRNAs in peritoneal fibrosis tissue was changed dynamically, and the difference was significant. Suggesting that lncRNA may play a key role in peritoneal fibrosis development and occurrence.
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