首页 | 本学科首页   官方微博 | 高级检索  
检索        

基因芯片筛选ghrelin miRNA转染胰腺炎细胞模型后的差异表达基因
引用本文:唐曦平,张露艺,梁志海,覃蒙斌,唐国都.基因芯片筛选ghrelin miRNA转染胰腺炎细胞模型后的差异表达基因[J].胃肠病学,2020(2):96-100.
作者姓名:唐曦平  张露艺  梁志海  覃蒙斌  唐国都
作者单位:广西医科大学附属肿瘤医院内镜中心;广西医科大学;广西医科大学第一附属医院消化内科;广西医科大学第二附属医院消化内科
基金项目:国家自然科学基金地区科学基金项目(81560111);广西高校中青年基础能力提升项目(2018KY0125);广西卫生厅立项项目(Z2015546)。
摘    要:背景:前期研究提示ghrelin在急性胰腺炎发病过程中发挥重要作用,但其机制尚不明确。目的:应用基因芯片技术筛选出ghrelin miRNA转染胰腺炎胰腺腺泡细胞后的差异表达基因。方法:以雨蛙肽构建胰腺炎胰腺腺泡细胞模型。将AR42J细胞分为ghrelin miRNA+雨蛙肽组、阴性对照+雨蛙肽组。提取细胞RNA,合成为ds-DNA,与大鼠全基因组基因芯片杂交、扫描、分析。筛选与炎症和钙通路相关的差异表达基因,并采用RT-PCR法对其中3个基因(Bcl-2、caspase-8、caspase-12)进行验证。结果:给予AR42J细胞ghrelin miRNA+雨蛙肽干预后,共筛选出2938个差异表达基因,其中1435个基因表达上调,1503个基因表达下调。与CAMP/Ca^2+信号通路相关的差异表达基因有60个,与炎症通路相关的差异表达基因有199个。RT-PCR结果表明,ghrelin miRNA+雨蛙肽组Bcl-2、caspase-12表达下调,caspase-8表达上调,与基因芯片筛查结果一致。结论:基因芯片技术可筛选出ghrelin miRNA转染胰腺炎胰腺腺泡细胞过程中发挥关键作用的基因,从而为研究内源性ghrelin对胰腺炎胰腺腺泡细胞的作用机制提供依据和参考。

关 键 词:基因芯片  胃促生长素  微RNAS  急性胰腺炎

Screening for Differentially Expressed Genes in Pancreatitis Cell Model Transfected With Ghrelin MiRNA by Gene Chip
TANG Xiping,ZHANG Luyi,LIANG Zhihai,QIN Mengbin,TANG Guodu.Screening for Differentially Expressed Genes in Pancreatitis Cell Model Transfected With Ghrelin MiRNA by Gene Chip[J].Chinese Journal of Gastroenterology,2020(2):96-100.
Authors:TANG Xiping  ZHANG Luyi  LIANG Zhihai  QIN Mengbin  TANG Guodu
Institution:(Department of Endoscope, Tumor Hospital Affiliated Guangxi Medical University, Nanning ,530021;Guangxi Medical University, Nanning;Department of Gastroenterology, the First Affiliated Hospital of Guangxi Medical University, Nanning;Department of Gastroenterology, the Second Affiliated Hospital of Guangxi Medical University, Nanning)
Abstract:Background:Previous studies suggest that ghrelin plays an important role in the pathogenesis of acute pancreatitis,but the mechanism is still unclear.Aims:To screen the differentially expressed genes in pancreatitis pancreatic acinar cells transfected with ghrelin miRNA by gene chip.Methods:Pancreatitis was induced by caerulin.AR42J cells were divided into ghrelin miRNA+caerulin group and negative control+caerulin group.AR42J cells were collected to extract RNA and synthesize ds-DNA,and was then hybridized with rat whole genome microarray for scanning and analyzing.Differentially expressed genes related to inflammation and calcium pathways were screened,and expressions of Bcl-2,caspase-8,caspase-12 were verified by RT-PCR.Results:For AR42J cells after intervention with ghrelin miRNA+caerulin,2938 differentially expressed genes were screened,including 1435 up-regulated genes and 1503 down-regulated genes.There were 60 differentially expressed genes involved in CAMP/Ca^2+signaling pathway and 199 differentially expressed genes involved in inflammation pathway.RT-PCR results showed that expressions of Bcl-2,caspase-12 were down-regulated and expression of caspase-8 was up-regulated in ghrelin miRNA+caerulin group,consistent with the results of gene chip.Conclusions:Gene chip can be used to screen the genes that play a key role in the process of pancreatitis pancreatic acinar cells transfected with ghrelin miRNA,and provide a theoretical basis and reference for the study of mechanism of endogenous ghrelin on pancreatitis pancreatic acinar cells.
Keywords:Gene Chip  Ghrelin  MicroRNAs  Acute Pancreatitis
本文献已被 CNKI 维普 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号