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作 者:董晓辉[1] 黄红铭[1] 徐瑞容[1] 薛英姿[1] 丁润生[2] 戚菁[1]
机构地区:[1]南通大学附属医院血液科,江苏226001 [2]南通大学附属医院外科综合实验室,江苏226001
出 处:《交通医学》2012年第1期29-32,共4页Medical Journal of Communications
基 金:南通市社会发展指导计划资助项目(S2009026)
摘 要:目的:研究多发性骨髓瘤细胞对人内皮细胞增殖、迁移、血管生成及对内皮细胞AKT、pAKT蛋白水平的影响。方法:采用多发性骨髓瘤细胞株U266与人脐静脉内皮细胞(HUVEC)混合共培养;以同期单独培养的HUVEC为对照,用CCK-8、划痕试验检测共培养组和对照组HUVEC的增殖、迁移能力。观察在Matrigel基质中两组HUVEC管状结构生成的情况;Western blot方法检测共培养组和对照组HUVEC AKT、pAKT的蛋白表达水平。结果:与同期单独培养的HUVEC相比,共培养体系中的HUVEC细胞增殖明显增加,共培养组HUVEC迁移能力明显增强(125±21/视野vs.332±37/视野),共培养组HUVEC管状结构形成数量明显增加(小管数量分别为3.7±1.3/视野vs.8.3±2.7/视野)。共培养体系中HUVEC pAKT表达水平明显升高,AKT表达无明显变化。结论:骨髓瘤细胞能明显促进血管内皮细胞增殖、迁移和血管生成。多发性骨髓瘤促进HUVEC增殖、迁移和血管生成的作用与AKT信号通路有关。Objective :To investigate the impact of human multiple myeloma cells U266 on human umbilical vein endothelial cells(HUVEC) proliferation,migration,angiogenesis,and the expression of AKT,pAKT.Methods:Multiple myeloma cells U266 and HUVEC were cultured as a mixed co-culture group to the same period HUVEC cultured alone as the control group to detect the proliferation of HUVEC in the two groups by CCK-8 and the migration of HUVEC and by scratch test to observe HUVEC angiogenesis in Matrigel matrix and to find the expression of AKT and pAKT in HUVEC of co-culture group by Western blot.Results:Compared with the control group,the number of HUVEC cells was markedly increased after co-culture.Migration of endothelial cells in co-culture group was significantly increased compared with that in the control group,the number being 125±21/HP and 332±37/HP.In the Matrigel matrix,the number of tube formation in endothelial cells of the co-culture group was significantly increased compared with that in the control group,the number being 3.7±1.3/HP and 8.3±1.3/HP.The expression of AKT and pAKT in HUVEC was significantly increased after co-cultured,but AKT protein expression was not statistically significant.Conclusion:Multiple myeloma cells can promote the HUVEC proliferation,migration and angiogenesis,showing that the promotion of multiple myeloma cells to HUVEC was related with the AKT signaling pathway.
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