| 刘夙璇 王国坤 董斐斐 丁雪燕 赵仙先 秦永文.大鼠心肌梗塞后心室重构中miRNA 的差异表达[J].,2014,14(12):2230-2233 |
| 大鼠心肌梗塞后心室重构中miRNA 的差异表达 |
| Differential Expression of miRNA in Ventricular Remodeling afterMyocardial Infarction in Rats |
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| DOI： |
| 中文关键词: 大鼠 心肌梗死 心室重构 微小RNA 表达差异 |
| 英文关键词: Rat Myocardial infarction Ventricular remodeling miRNA Differential expression |
| 基金项目:上海市卫生局科研基金项目(20134089)，长海医院1255 科研基金项目(CH125542700) |
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| 中文摘要: |
| 目的：筛选大鼠急性心梗后的心室重构过程中差异表达的微小RNA(microRNA, miRNA)，为miRNA 调控心室重构的机制
研究提供靶标。方法：20 只成年雄性Wistar 大鼠，分组如下：心肌梗死组(MI组，n=10)和假手术组(Sham 组，n=10)。通过结扎大鼠
左冠状动脉前降支构建急性心梗模型建模。4 周后对大鼠进行超声心动图检查和梗死边缘区心肌HE 染色观察心室重构程度。利
用miRNA芯片对心梗边缘区的miRNA进行差异表达检测，采用实时定量PCR验证芯片结果的可靠性。结果：心脏超声显示MI
组大鼠左室重构明显，心梗边缘区心肌HE染色可见细胞间质大量胶原纤维沉积。miRNA 芯片结果显示15 个miRNA在心梗4
周后呈差异表达，其中11 个miRNA(miR-21、miR-23a、miR-125b、miR-132、miR-146b、miR-181b、miR-199a、miR-320、miR-324、
miR-328 和miR-499)表达上调，4 个miRNA(miR-29、miR-30c、miR-133a 和miR-208)表达下调。实时定量PCR 验证结果与芯片结
果一致。结论：这些差异表达的miRNA 可能与心梗后心室重构相关，进一步深入研究特定miRNA 的调控机制有望为基因治疗提
供新靶点。 |
| 英文摘要: |
| Objective:To screen the miRNA differential expression profile in ventricular remodeling after myocardial infarction in
rats and identify the target of miRNA in the mechanism of ventricular remodeling.Methods:A total of 20 male Wistar rats were
randomly assigned into MI group (n=10) and Sham group (n=10). MI rats were induced by ligation of the anterior descending coronary
artery. Four weeks later, ventricular remodeling were measured by echocardiography and HE staining. The miRNA in the cardiac tissues
of border zone were measured by miRNA microarray. The miRNA that expressed significantly differently would be verified by Real time
quantitative PCR.Results:Echocardiographic results showed serious ventricular remodeling in the MI rats. HE staining revealed
significant collagen deposition around the border area of the infarct region. By significance analysis of microarray based on microarray
screening, 15 significantly different expression of miRNA were obtained after myocardial infarction for 4 weeks. 11 miRNA were
significantly up-regulated (miR-21, miR-23a, miR-125b, miR-132, miR-146b, miR-181b, miR-199a, miR-320, miR-324, miR-328 and
miR-499) and 4 miRNA were significantly down-regulated (miR-29, miR-30c, miR-133a and miR-208). Real time quantitative PCR
approved the results as well.Conclusion:These significantly differently expressed miRNA might be related with ventricular remodeling
after myocardial infarction and further studies of the mechanismof some specific miRNA would be a new target of gene therapy. |
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