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作 者:梁嘉斌[1] 林育纯[1] 方飞[1] 陈雯[1] 陈成章[1] 林忠宁[1]
机构地区:[1]中山大学公共卫生学院预防医学系,广东广州510080
出 处:《中国职业医学》2007年第4期265-267,270,共4页China Occupational Medicine
基 金:国家自然科学基金资助课题(No.30471428);广东省自然科学基金资助课题(No.05001765)
摘 要:目的 探讨镉化合物对人树突状细胞(DC)的细胞毒性作用。方法 应用粒-巨噬细胞集落刺激因子(GM-CSF)+白细胞介素-4(IL-4)和肿瘤坏死因子-α(TNF-α)诱导人外周血单核细胞获得DC,流式细胞仪(FACS)检测细胞表面标记鉴定;给予CdCl2处理进行剂量-效应和时间-效应分析,采用甲基四氮唑盐(MTS)颜色反应法检测细胞毒性作用。结果 诱导获得的DC呈悬浮生长,部分细胞聚集成簇。细胞表面标志分子表达阳性CD14为2.7%,HLA-DR为96.3%,CD1a为83.9%,CD80为88.3%,CD83为58.8%,CD86为42.4%。不同剂量(1.25-80.00μmol/L)和作用时间(24-48h)CdCl2染毒组细胞增殖抑制率不同程度增高,呈剂量-和时间-依赖性关系。结论 诱导获得成熟的人DC;镉作用可致成熟DC的细胞毒性效应。Objective To study the cytotoxicity of cadmium compound on dendritic cells (DC). Methods Human peripheral blood monocytes ( PBMC ) from healthy donors were induced with GM-CSF + IL-4 and TNF-α to harvest DC. The surface markers on DC were analyzed by Flow cytometry. The MTS assay was conducted to evaluate the proliferative function of matured DC treated by CdCl2 in a dose-effect ( 1.25 - 80. 00 μmol/L) and time-course ( 24 - 48 hours ) studies. Results The induced DC growed suspendedly and aggregated into clumps with typical morphology. There was high level expression simultaneously in HLADR (96. 3% ), CD1a (83.9%), CDSO (88.3%),CD83 (58.8%) and CD86 (42. 4%), hut low level in CD14 (2. 7%). The cellular proliferation inhibition rate of DC significantly increased in cadmium-treated groups in dose- and time-dependent patterns. Conclusion It was shown that there was inducible cytotoxic effect of CdCl2 on human matured DC.
分 类 号:R135.1[医药卫生—劳动卫生] R994.3[医药卫生—公共卫生与预防医学]
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