IKKε基因敲除小鼠血管内皮细胞的原代培养及鉴定
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国家自然科学基金面上项目(81070180);国家人力资源和社会保障部留学人员科技活动项目(人社厅函[2010]412号)


Culture of vascular endothelial cells from IKKε KO mouse artery
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    摘要:

    目的:建立简单有效地获取I-资B激酶复合物-着(inhibitor--资B kinase -着,IKK-着)基因敲除小鼠血管内皮细胞的培养方法-方法:在超净台中取小鼠主动脉,撕去其外膜和脂肪组织,纵行剖开血管,切成1 mm × 1 mm的血管块,内面朝下贴于培养皿底部,加入含内皮细胞生长辅助因子(ECGS)的DMEM培养液,贴壁培养;用倒置显微镜观察细胞形态并用Ⅷ因子相关抗原免疫荧光的方法进行鉴定-结果:72 h后在倒置显微镜下可见内皮细胞从血管块边缘游出,12~14 d血管内皮细胞融合成片,Ⅷ因子相关抗原免疫荧光检测呈阳性-结论:本方法可获取纯度高-结构和功能良好的IKKε基因敲除小鼠血管内皮细胞-

    Abstract:

    Objective:To develop an easy and reduplicate method for the isolation and primary culture of vascular endothelial cells of I-资B kinase ε(IKKε) knock-out(KO) mouse. Method: The aorta was obtained from IKKε KO mouse in the super-clean bench,with its adventitia and adipose tissue cleared carefully. Then the vessel was split longitudinally and cut into 1 mm × 1 mm explants. The explants were placed on culture dish with the lining endothelium side down and DMEM containing endothelial cell growth supplement(ECGS) was added into the culture dish. The morphological characteristics of the cells were observed with the inverted microscope and the cells were evidenced by immunofluorescence with marker Ⅷ factor. Results: Endothelial cells migrating out of the aortic intima can be seen at the edge after 72 hours,forming confluent monolayer 12~14 days later. Immunofluorescence showed the characteristic positive reaction of Ⅷ factor in the cytoplasm of the cells. Conclusion: High purity,solid structure and sound function IKKε KO mouse endothelial cells can be obtained from this method.

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戚永超,陈 文,朱一帆,万 辛,曹长春,陈 鑫. IKKε基因敲除小鼠血管内皮细胞的原代培养及鉴定[J].南京医科大学学报(自然科学版),2012,(3):329-332

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  • 收稿日期:2011-12-16
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