首页 | 本学科首页   官方微博 | 高级检索  
     

RNA干扰内皮细胞分泌白细胞介素6影响平滑肌细胞的迁移
引用本文:王 刚,刘朝中,宋云龙,张晓慧,张 丽,李 力,曹俊涵,张红超. RNA干扰内皮细胞分泌白细胞介素6影响平滑肌细胞的迁移[J]. 中国组织工程研究, 2011, 15(37): 6932-6936. DOI: 10.3969/j.issn.1673-8225.2011.37.022
作者姓名:王 刚  刘朝中  宋云龙  张晓慧  张 丽  李 力  曹俊涵  张红超
作者单位:解放军空军总医院,心血管内科, CT/MRI室,心血管外科,北京市 100142;解放军第452医院心血管内科,四川省成都市 610041; 四川抗菌素工业研究所,四川省成都市 610000
基金项目:国家自然科学基金(30872539),课题名称:干扰白细胞介素6在心力衰竭中的作用。
摘    要:背景:血管支架置入后靶血管部位易发生炎症反应。目的:利用siRNA技术抑制内皮细胞白细胞介素6的生成,观察其对平滑肌细胞迁移的影响。方法:采用RT-PCR测定脂多糖刺激EA.HY926细胞表达白细胞介素6 mRNA的时间梯度与浓度梯度,针对白细胞介素6构建短发卡状siRNA真核表达载体pGensil-1.1-白细胞介素6,通过lipofectamine 2000转染EA.HY926,抑制其白细胞介素6的产生。结果与结论:pGensil-1.1-白细胞介素6转染EA.HY926细胞后,脂多糖刺激下EA.HY926细胞表达的白细胞介素6 mRNA及蛋白明显减少。共培养模型中,转染pGensil-1.1-白细胞介素6的EA.HY926细胞作用下,人脐静脉平滑肌细胞表达的基质金属蛋白酶9 mRNA及蛋白明显降低,结晶紫染色显示人脐静脉平滑肌细胞迁移数量减少。说明siRNA技术可抑制内皮细胞白细胞介素6的生成,并通过降低平滑肌细胞基质金属蛋白酶9的表达减弱平滑肌细胞的迁移能力。

关 键 词:共培养  基因干扰  白细胞介素6  基质金属蛋白酶9  支架再狭窄  平滑肌细胞  迁移  
收稿时间:2011-03-19

Effects of RNA interference on interleukin-6 expression in endothelial cells and migration of vascular smooth muscle cells
Wang Gang,Liu Chao-zhong,Song Yun-long,Zhang Xiao-hui,Zhang Li,Li Li,Cao Jun-han,Zhang Hong-chao. Effects of RNA interference on interleukin-6 expression in endothelial cells and migration of vascular smooth muscle cells[J]. Chinese Journal of Tissue Engineering Research, 2011, 15(37): 6932-6936. DOI: 10.3969/j.issn.1673-8225.2011.37.022
Authors:Wang Gang  Liu Chao-zhong  Song Yun-long  Zhang Xiao-hui  Zhang Li  Li Li  Cao Jun-han  Zhang Hong-chao
Affiliation:Department of Cardiovascular Medicine, CR/MRI Room, Department of Cardiovascular Surgery, PLA  Airforce General Hospital, Beijing 100142, China; Department of Cardiovascular Medicine, the 452 Hospital of Chinese PLA, Chengdu 610041, Sichuan Province, China; Department of Sichuan Industrial Institute of Antibiotics Co., Ltd., Chengdu 610000, Sichuan Province, China
Abstract:BACKGROUND:Inflammatory reaction easily occurs in target vascular region after implantation of intravascular stent.OBJECTIVE:To investigate the effects of siRNA technique on migration of vascular smooth muscle cells by inhibiting the expression of interleukin-6 (IL-6) in the endothelial cells. METHODS:The time gradient and concentration gradient of the IL-6 mRNA expression in the EA.HY926 cells stimulated by lipopolysaccharide (LPS) were detected by RT-PCR. Short hairpin RNA eukaryotic expression vector targeting IL-6 gene, named pGensil-1.1-IL-6, was constructed and transfected into EA.HY926 cells for intervention of IL-6 expression by lipofectamine 2000. RESULTS AND CONCLUSION:After pGensil-1.1-IL-6 was transfected into EA.HY926 cells, IL-6 mRNA and protein expression in the EA.HY926 cells stimulated by LPS was obviously decreased. In co-culture model, under the effect of EA.HY926 cells transfected by pGensil-1.1-IL-6, matrix metalloproteinase 9 mRNA and protein expression in the human cord venous smooth muscle cells was obviously decreased. The number of human cord venous smooth muscle cells was decreased. These findings suggest that siRNA technique can inhibit the expression of IL-6 in endothelial cells and attenuate the migration of smooth muscle cells by decreasing matrix metalloproteinase 9 expression.
Keywords:
点击此处可从《中国组织工程研究》浏览原始摘要信息
点击此处可从《中国组织工程研究》下载全文
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