转录因子MCPIP在大鼠动脉粥样硬化病变进程中的表达

    Expression of transcription factor MCPIP in atherosclerotic lesions in rats

    • 摘要: 目的 观察转录因子MCPIP在大鼠动脉粥样硬化(AS)病变过程中的表达。方法 将60只SD大鼠随机分为4个模型组和4个空白组;用喂饲高脂饲料加维生素D3灌胃的方法建立大鼠AS模型:分别建模2、4、6和7周,每一模型组设置相应空白组,喂饲普通饲料;HE染色观察各组大鼠胸主动脉病理改变;Real Time-PCR检测各组血管中MCPIP mRNA转录量;免疫组化检测各组血管中MCPIP蛋白表达量。结果 病理结果显示建模2周后,大鼠血管即出现AS病变,随着建模时间的延长,AS病变逐渐加重;Real Time-PCR结果显示,随着建模时间延长,各模型组血管中MCPIP mRNA的表达呈上升趋势;4个模型组与同期空白组比较,MCPIP mRNA的表达均有显著升高,差异明显(P<0.05或P<0.01);免疫组化结果显示:随着建模时间延长,MCPIP蛋白表达量也呈上升趋势;4个模型组MCPIP蛋白表达量均高于同期空白组,有显著差异(P<0.05或P<0.01)。结论 随着AS大鼠模型建模时间延长,胸主动脉AS病变逐渐加重,血管中MCPIP的mRNA及蛋白表达量也呈递增变化,提示MCPIP在AS病变发生发展中有重要作用。

       

      Abstract: AIM To investigate the expression of monocyte chemotactic protein-induced protein( MCPIP) in the process of atherosclerosis in rats. METHODS Sixty Sprague Dawley rats were randomly divided into four model groups and four control groups. Atherosclerosis was established by feeding rats with a high-fat diet and gavage of vitamin D3 for 2,4,6 and 7 weeks,respectively. Control rats were fed with a normal diet. The pathological changes of thoracic aorta were observed by HE staining.mRNA levels of MCPIP in thoracic aorta were determined by real time-PCR and MCPIP protein was detected by immunohistochemistry. RESULTS Pathological examination showed that atherosclerotic lesions occurred 2 weeks after treatment and progressed with time. Real-time PCR results showed that vascular MCPIP mRNA increased in model rats compared with that in controls( P < 0. 05 or P < 0. 01).Immunohistochemistry showed increased expression of MCPIP protein with time. Expression of MCPIP protein in four model groups were significantly higher than in the corresponding normal control groups( P <0. 05 or P <0. 01). CONCLUSION We successfully established atherosclerosis in rats by feeding a high-fat diet plus vitami D3. Thoracic aortic atherosclerotic lesions occur 2 weeks after treatment and gradually are aggravated. Expressions of vascular MCPIP mRNA and protein increase after treatment,suggesting that MCPIP plays an important role in the development of atherosclerotic lesions.

       

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