摘要
目的探讨^125I-脱氧尿嘧啶核苷(^125I-UdR)在淋巴瘤细胞Raji和Daudi中的特异性摄取及其杀伤效应。方法测量Raft、Daudi细胞和细胞核在含不同放射性浓度^125I-UdR的培养液中培养不同时间后的活度;用噻唑蓝(MTT)实验和碘化丙啶(PI)染色周期分析评价^125I-UdR对Raji和Daudi细胞的杀伤作用。结果Raji和Daudi细胞摄取^125I-UdR的量明显高于Na^125I对照组(P〈0.05),在100kBq/ml浓度时,Raji和Daudi细胞摄取^125I-UdR的量分别为(14414±95)和(6916±53.69)Bq/10^6细胞,而对Na^125I的摄取量分别为(68±3.8)和(324±32.8)Bq/10^6细胞;细胞和细胞核中^125I-UdR的量随培养基中^125I-UdR放射性浓度以及培养时间的增加而增加;^125I-UdR组的存活分数明显低于Na^125I对照组(P〈0.05),以500kBq/ml浓度培养48h时,Raji和Daudi细胞^125I.UdR组的存活分数分别为(19.78±1.39)%和(43.17±2.69)%,而Na^125I组的存活分数分别为(79.10±1.79)%和(80.36±6.12)%;细胞存活分数有随培养基中放射性浓度增加而降低的趋势。结论^125I-UdR可被Raji和Daudi细胞特异性摄取并进入细胞核中,进而杀死细胞,其作用具有明显的时间-效应和剂量-效应关系。
Objective To evaluate the killing effect and the uptake of ^125I-UdR on human lymphoma Raji and Daudi cell lines. Methods The amount of ^125I-UdR in the cells and cell nuclei were determined after incubation of different time in RPMI 1640 culturing medium containing different concentrations of ^125I-UdR. The killing effects of ^125I-UdR on Raji and Daudi cell lines were estimated through MTF assay and cell cycle was analyzed by propidium iodide (PI) staining. Results The amounts of ^125I-UdR in Raji and Daudi ceils and cell nuclei were much higher than that of Na^125I( P 〈 0.05). The amounts of ^125I-UdR in Raji and Daudi cells were 14 414 ± 95 and (6916 ± 53.69) Bq/10^6 cell when the concentration was 100 kBq/ml. The amounts of Na^125I were 68 ± 3.8 and (324 ± 32.8) Bq/10^6 cell. The uptake of ^125I-UdR in Raji and Daudi cells and cell nuclei increased with the ^125I-UdR concentration and incubated time. The cell surviving fractions of ^125I-UdR groups was much lower than that of Na^125Igroups (P 〈 0.05). When the concentration was 500 kBq/ml and incubated time was 48 hours, the Raji and Daudi cell surviving fractions of ^125I-UdR groups were (19.78 ± 1.39)% and (43.17±2.69)%; those of Na^125I groups were( 79.10 ± 1.79)% and (80.36 ± 6.12)%. The surviving fractions of ^125I-UdR groups reduced with the ^125I -UdR concentration. Conclusions ^125I-UdR can be specially ingested by Raji and Daudi cells and incorporated into DNA, then the cells will be killed. The uptake of ^125I-UdR is dose and time dependent.
出处
《中华放射医学与防护杂志》
CAS
CSCD
北大核心
2009年第1期50-53,共4页
Chinese Journal of Radiological Medicine and Protection