Rithidech Kanokporn Noy, Tungjai Montree, Arbab Edgar, Simon Sanford R
Pathology Department, State University of New York at Stony Brook, Stony Brook, NY 11794-8691, USA.
Radiat Environ Biophys. 2005 Oct;44(2):139-43. doi: 10.1007/s00411-005-0004-5. Epub 2005 Nov 2.
We measured levels of NF-kappaB activation in bone marrow (BM) cells collected at 1 and 4 h from male BALB/cJ mice (10-12 weeks old) given a whole body dose of 0, 0.05, 0.1 and 1 Gy of (137)Cs gamma-rays (at the dose rate of 0.75 Gy/min). At each harvest time-point, BM cells were collected from five mice per dose of radiation. We used two methods for detecting NF-kappaB activation (1) the NF-kappaB/p65 transcription factor enzyme-linked immunosorbance assay (ELISA) and (2) immunofluorescence staining with NF-kappaB/p65 antibody. Results from ELISA indicated 2.0 and 2.8-fold increases in NF-kappaB activation in BM cells isolated at 1 h post-exposure of mice to 0.1 or 1.0 Gy. The immunofluorescence staining method showed similar results. In samples isolated 4 h post-irradiation, however, no activated NF-kappaB signal was found, regardless of the method of detection. The data also demonstrated that NF-kappaB was not activated in bone marrow cells collected either at 1 or 4 h from BALB/cJ mice exposed to a single dose of 0.05 Gy (137)Cs gamma-rays. Taken together, the results from our in vivo study indicate the involvement of NF-kappaB activation in early response to 0.1 and 1.0 Gy (but not 0.05 Gy) of (137)Cs gamma-rays.
我们测量了雄性BALB/cJ小鼠(10 - 12周龄)在接受全身剂量为0、0.05、0.1和1 Gy的¹³⁷Csγ射线(剂量率为0.75 Gy/min)照射后1小时和4小时收集的骨髓(BM)细胞中NF-κB的激活水平。在每个收获时间点,从每剂量辐射的五只小鼠中收集BM细胞。我们使用两种方法检测NF-κB的激活:(1)NF-κB/p65转录因子酶联免疫吸附测定(ELISA)和(2)用NF-κB/p65抗体进行免疫荧光染色。ELISA结果表明,在小鼠暴露于0.1或1.0 Gy后1小时分离的BM细胞中,NF-κB激活增加了2.0倍和2.8倍。免疫荧光染色方法显示了类似的结果。然而,在照射后4小时分离的样本中,无论检测方法如何,均未发现激活的NF-κB信号。数据还表明,在暴露于单剂量0.05 Gy¹³⁷Csγ射线的BALB/cJ小鼠1小时或4小时收集的骨髓细胞中,NF-κB未被激活。综上所述,我们体内研究的结果表明NF-κB激活参与了对0.1和1.0 Gy(但不是0.05 Gy)¹³⁷Csγ射线的早期反应。