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机构地区:[1]华中科技大学同济医学院附属协和医院,武汉430022
出 处:《神经损伤与功能重建》2011年第2期79-83,共5页Neural Injury and Functional Reconstruction
摘 要:目的:探讨重组人促红细胞生成素(rH-EPO)对缺血缺氧损伤内皮细胞的血管新生作用及其可能机制。方法:氧糖剥夺-复氧复糖(OGD/R)损伤内皮细胞株EA.hy926,复氧复糖过程中添加rH-EPO;采用MTT还原法、Transwell小室迁移实验及Matrigel小管形成实验评价内皮细胞血管新生能力;ELISA法检测培养上清液血管内皮生长因子(VEGF)含量;实时PCR法分析内皮型一氧化氮合酶(eNOS)mRNA变化;Western Blot法分析eNOS蛋白变化。结果:OGD诱导EA.hy926细胞受损,降低其增殖、迁移和管样结构形成能力,VEGF含量减少,eNOS基因及其蛋白表达均下降;rH-EPO干预后,受损细胞的增殖、迁移和管样结构形成能力提高,VEGF含量、eNOS基因及其蛋白表达均增加(均P<0.05)。结论:rH-EPO可促进受损内皮细胞血管新生,VEGF和eNOS可能参与rH-EPO诱导的血管新生过程。Objective: To study the angiogenic role of recombinant human erythropoietin(rH-EPO) on EA.hy926 cells after oxygen and glucose deprivation followed by reoxygenation(OGD/R) in vitro.Methods: Cells were subjected to OGD/R and stimulated by rH-EPO during the reoxygenation procedure.MTT assay,Transwell assay and Matrigel assay were used to detect the angiogenic ability of cells post-OGD.The expressions of vascular endothelial growth factor(VEGF),endothelial nitric oxide synthase(eNOS) mRNA and eNOS protein were also detected.Results: OGD induced a significant decrease in proliferation,migration,and tube formation ability of EA.hy926 cells and the expression of VEGF,eNOS mRNA and protein were significantly decreased.rH-EPO mitigated the OGD-induced damage of proliferation,migration,and tube formation ability of cells and increased the expression of VEGF,eNOS mRNA and protein.Conclusion: VEGF and eNOS probably play critical roles in the angiogenic effects of rH-EPO on cells after OGD.
关 键 词:重组人促红细胞生成素 血管新生 氧糖剥夺 血管内皮生长因子 内皮型一氧化氮合酶
分 类 号:R741[医药卫生—神经病学与精神病学] R741.05[医药卫生—临床医学]
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