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作 者:尹扬光[1] 黄岚[1] 赵晓辉[1] 方玉强[1] 周健[1] 赵景红[1] 陈剑飞[1] 崔斌[1]
机构地区:[1]第三军医大学新桥医院全军心血管内科研究所,重庆400037
出 处:《心血管康复医学杂志》2006年第5期427-430,434,共5页Chinese Journal of Cardiovascular Rehabilitation Medicine
基 金:国家自然科学基金资助项目(项目编号/申请代码:30470729/C03030201)
摘 要:目的:观察基质细胞衍生因子-1(SDF-1)对体外培养的小鼠骨髓源性内皮祖细胞(EPC s)数量及功能的影响。方法:以密度梯度离心法获取小鼠骨髓单个核细胞(M NC s),由BS-1和D iI-acLDL荧光双染鉴定。加入不同浓度SDF-1 a培养48 h,然后分别采用M TT法、改良的Boyden小室和粘附能力测定来观察EPC s的增殖、迁移和粘附能力;采用血清饥饿法和紫杉醇诱导EPC s凋亡,TUNEL法和流式细胞仪检测SDF-1a对EPC s凋亡率的影响。结果:SDF-1a剂量依赖性增加EPC s数量(P<0.01),并显著改善了EPC s的粘附、迁移和增殖能力(P<0.01),显著降低EPC s凋亡率(P<0.01)。结论:SDF-1a可增加小鼠骨髓源性EPC s的数量并改善EPC s功能。Objective: To study whether SDF-1 has effects on endothelial progenitor cells (EPCs). Methods: Total mononuclear cells (MNCs) isolated from bone marrow by density gradient centrifugation combined with adherence ceils filtration were plated on fibronectin coated culture dishes. After 7 days, adherent cells were kept with different concentrations of SDF-1a for 48 hours. EPCs proliferation, migration ability and adhesion assay was performed: EPCs apoptosis was induced by paclitaxel or serum starvation for 48h, apoptosis was determined by TUNEL method and flow cytometry. Results : Incubation of SDF-1a dose dependently increased the number of EPCs (P〈0. 01) : SDF -1a improved EPCs proliferation, migration and adhesive capacity (P〈0. 01), and SDF-1a could protect EPCs from paclitaxel or serum starvation-induced apoptosis (P〈0. 01). Conclusion: SDF-1a can increase the number of bone marrow derived EPCs and improve their biological characteristics.
关 键 词:基质细胞衍生因子-1 内皮细胞 细胞增殖 细胞凋亡
分 类 号:R329.2[医药卫生—人体解剖和组织胚胎学]
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