摘要
对浓缩铀235U内照射人淋巴细胞白血病细胞株Molt4细胞和巨噬细胞株Ana1细胞诱发的细胞凋亡及细胞因子的防护作用进行了研究。实验中估算了235U在不同阶段培养细胞中的辐射累积吸收剂量。通过荧光显微镜形态观察,发现免疫细胞在受235U辐照后,可诱发明显的以核断裂和核固缩为特征的细胞凋亡。微观放射自显影研究显示,235U可迅速被免疫细胞吞噬,在细胞内以吞噬小泡的形式均匀地弥散于胞浆和胞核内。研究发现,IL2和IL6这两个细胞因子对由235U诱发的免疫细胞DNA链断裂具有显著的防护作用。研究结果对于临床上寻找提高内照射放射治疗病例的免疫功能措施,具有一定的价值。
Cell apoptosis in human acute lymphoblastic cell line Molt 4 and macrophage cell line Ana 1 was induced by 235 U. The cumulative radiation absorption doses of 235 U in cultured cells through different periods were estimated. The morphological changes in Molt 4 and Ana 1 cells were observed by fluorescence microscopy. We found that Molt 4 and Ana 1 cells, internally irradiated by 235 U, displayed a significant nuclear fragmentation and a marked pyknosis. The microautoradiographic study showed that at first 235 U was phagocytized by Molt 4 and Ana 1 cells, and then 235 U was homogeneously distributed through the cells. The finding indicated that 235 U can significantly increase the DNA fragmentation and apoptotic bodies formation in the immune cells, and this effect could be inhibited by IL 2 and IL 6. So both IL 2 and IL 6 showed radioprotective effect on Molt 4 and Ana 1 cells internally irradiated by 235 U.
出处
《辐射研究与辐射工艺学报》
CAS
CSCD
北大核心
1998年第4期241-243,共3页
Journal of Radiation Research and Radiation Processing
基金
国家核工业科学基金