γ射线诱发培养淋巴细胞TCR基因突变的剂量-效应关系  被引量:7

The dose-response relationship of T-cell receptor gene mutation induced by gamma-ray in cultured lymphocytes

在线阅读下载全文

作  者:刘长安[1] 

机构地区:[1]北京大学第三医院肿瘤与放射病研究室,北京100083

出  处:《中国工业医学杂志》2005年第1期23-25,共3页Chinese Journal of Industrial Medicine

基  金:国家科技部社会公益研究专项资金项目 (2 0 0 1DIB2 0 1 0 8)

摘  要:目的 探讨γ射线诱发培养淋巴细胞T细胞受体 (TCR)基因突变的剂量 效应关系。方法 以不同剂量 (0~ 4 0Gy)的γ射线照射新鲜分离的健康成人外周血淋巴细胞 ,植物血凝素脉冲式刺激 2h后 ,用白细胞介素- 2培养 7d ,用单克隆抗体直接免疫荧光标记流式细胞术检测TCR基因突变频率 (TCRMF)。应用SAS统计软件包编写的程序进行辐射剂量 效应曲线的拟合和筛选。结果 培养 7d后 ,TCRMF (10 -4)随照射剂量D (Gy)的增加而增高 ,最佳拟合曲线为二次多项式模型 ,其方程式可描述为 :TCRMF =2 . 74+ 6. 0 5D + 7 60D2 (F =3 62. 3 7 16,P <0 . 0 1,经校正的R2 =0 . 9999)。结论 TCR基因突变作为一种有潜力的生物剂量计可能用于近期辐射照射生物剂量的估算。Objective To investigate the dose-response relationship of T-cell receptor(TCR)gene mutation induced by gamma-ray in cultured lymphocytes.Method Freshly isolated peripheral lymphocytes from healthy adult donors were irradiated with gamma-ray in doses ranging from 0 Gy to 4.0 Cy and cultured with interleukin-2 for 7 days after phytohemagglutinin pulse stimulation for 2 h.The mutant frequencies of TCR gene(TCR MF)were detected by flow cytometry with direct immunofluorescence.Radiation dose-response curves were fitted and an optimal mathematical model for it was selected with programs programmed with Statistical Analysis System(SAS)soft package.Result TCR MF(unit is 10 -4 )increased dose D(in Gy)dependently after cultured for 7 days.Data were found to be fitted optimal by a quadratic polynomial dose-response model,which could be described by the formula TCR MF=2.74+6.05D+7.60D 2(F=36 237.16,P<0.01,adjusted R 2=0.999 9).Conclusion It is suggested that TCR gene mutation,which served as a potential biological dosimeter,may be applied for the estimation of biological dose for recent radiation exposure.

关 键 词:辐射照射 基因突变 T细胞受体基因 剂量-效应模型 生物剂量计 

分 类 号:R14[医药卫生—公共卫生与预防医学] Q754[生物学—分子生物学]

 

参考文献:

正在载入数据...

 

二级参考文献:

正在载入数据...

 

耦合文献:

正在载入数据...

 

引证文献:

正在载入数据...

 

二级引证文献:

正在载入数据...

 

同被引文献:

正在载入数据...

 

相关期刊文献:

正在载入数据...

相关的主题
相关的作者对象
相关的机构对象