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作 者:章必成[1] 王俊[1] 赵勇[2] 高建飞[2] 郭燕[1] 陈正堂[1]
机构地区:[1]第三军医大学新桥医院全军肿瘤研究所,重庆400037 [2]广州军区武汉总医院肿瘤科,湖北武汉430070
出 处:《武汉大学学报(医学版)》2007年第3期274-278,共5页Medical Journal of Wuhan University
基 金:国家自然科学基金资助项目(编号:30371586)
摘 要:目的:探讨不同活化表型的巨噬细胞对淋巴管内皮细胞(LEC)增殖、迁移和管样结构形成的影响。方法:分别以mrIFN-γ、mrIL-4处理小鼠RAW264.7细胞,建立经典活化的巨噬细胞(caMphi)和替代性活化的巨噬细胞(aaMphi)模型。采用transwell系统,将活化的巨噬细胞和LEC共培养。通过绘制细胞生长曲线、细胞迁移实验和基质胶实验,分别观察它们对LEC增殖、迁移和管样结构形成的影响。结果:与aaMphi共培养的LEC增殖速度较快,迁移能力和管样结构形成能力均明显强于其它对照组。结论:aaMphi能够促进LEC增殖、迁移和管样结构形成。Objective: To explore the effect of macrophages with different activated phenotypes on the proliferation, migration and tube-like structure formation of lymphatic endothelial cells (LEC).Methods: Classically activated macrophages (caMphi) and alternatively activated macrophages (aaMphi) models were established by RAW264.7 macrophages treated with mrIFN-γ and mrIL-4. Based on the co-culture systems of activated macrophages and LEC, cell growth curve, migration assay and matrigel assay were used to observe the effect of macrophages on the proliferation,migration and tube-like structure formation of LEC. Results. The proliferation of LEC co-cultured with aaMphi was faster, and their ability to migrate and form tube-like structure was signif-icantly stronger than that in the other groups. Conclusion. aaMphi can promote the proliferation,migration and tube-like structure formation of LEC.
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