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雷公藤甲素对血管生成的抑制作用
引用本文:丁怡,张建成,侯立军,张杰,王秋林,王树人.雷公藤甲素对血管生成的抑制作用[J].生物医学工程学杂志,2005,22(4):778-781.
作者姓名:丁怡  张建成  侯立军  张杰  王秋林  王树人
作者单位:1. 四川大学,华西基础与法医学院,病理生理教研室,成都,610041
2. 四川大学,华西医院,消化外科,成都,610041
3. 潍坊医学院,体育教研室,潍坊,261042
4. 潍坊医学院,眼科,潍坊,261042
基金项目:山东省教育厅资助课题(J01K08)
摘    要:利用体外培养人脐静脉内皮细胞,经不同浓度的雷公藤甲素(0、5、10、20、30μg/L)处理后,MTT法显示雷公藤甲素可抑制内皮细胞的增殖,5μg/L雷公藤甲素的抑制率达29.15%;琼脂凝胶立体细胞培养系统检测发现内皮细胞经雷公藤甲素作用后,其游走能力降低;鸡胚尿囊膜试验观察到雷公藤甲素可有效抑制血管的生成;荧光定量RT-PCR检测发现雷公藤甲素可下调内皮细胞u-PAmRNA的表达。因此认为,雷公藤甲素可能在基因水平上干扰内皮细胞u-PAmRNA的表达,减少u-PA蛋白的生成,从而有效地抑制血管内皮细胞的增殖和移行,这可能是雷公藤甲素抑制血管生成的主要机制之一。

关 键 词:雷公藤甲素  内皮细胞  尿激酶型纤溶酶原激活物  血管生成  荧光定量RT-PCR
收稿时间:2005-01-06
修稿时间:2005-01-062005-03-18

Effects of Triptolide on Anti-angiogenesis by Reducing Expression of Urokinase Plasminogen Activator
Ding Yi,ZHANG Jiancheng,HOU Lijun,Zhang Jie,Wang Qiulin,WANG Shuren.Effects of Triptolide on Anti-angiogenesis by Reducing Expression of Urokinase Plasminogen Activator[J].Journal of Biomedical Engineering,2005,22(4):778-781.
Authors:Ding Yi  ZHANG Jiancheng  HOU Lijun  Zhang Jie  Wang Qiulin  WANG Shuren
Institution:Department of Pathophysiology, West China School of Basic Medical Sciences and Forensic Medicine, Sichuan University, Chengdu, China.
Abstract:In order to unveil the anti-angiogenic mechanism of triptolide, we investigated the effects of triptolide on the proliferation, migration, angiogenesis and u-PA expression of cultured HUVECs. MTT assay found that triptolide could inhibit the proliferation of HUVECs,and three-dimensional culture system revealed that triptolide could curb the migration of HUVECs. The chick embryo chorioallantoic membrane (CAM) test showed that triptolide could inhibit angiogenesis. Real time quantitive RT-PCR showed the expression of u-PA of HUVECs was down-regulated by triptolide. Therefore, triptolide may inhibit the proliferation and migration of endothelial cell by way of reducing the expression of u-PA. These findings may conduce to the elucidation of the anti-angiogenic mechanism of triptolide.
Keywords:Triptolide Endothelium u-PA Angiogenesis Real-time quantitative RT-PCR  
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