Harris G, Sljivić V
Immunology. 1972 Aug;23(2):147-58.
The acute effects of various doses of whole body X-radiation on the splenic PFC of mice responding to primary and secondary immunization with SRC were studied. The results showed that suppression of plaque-forming capacity occurred 2 hours after varying doses of X-rays and was very severe by 6 hours. No differences in sensitivity were seen at any stage of the primary or secondary response examined. This acute depressive effect showed that the maintenance of splenic PFC was highly sensitive to radiation and was associated with a severely reduced uptake of [H]thymidine into the spleen at the same time after irradiation. Since previous studies (Harris and Pelc, 1970) have shown that incorporation of [H]thymidine occurred in non-dividing cells in mouse spleen, it was concluded that this turnover of DNA was important for the development of the capacity of cells to produce specific antibodies and that the acute depressive effects of X-radiation on splenic PFC was primarily due to inhibition of this process.
研究了不同剂量的全身X射线辐射对用SRC进行初次和二次免疫的小鼠脾脏中产生抗体的细胞(PFC)的急性影响。结果表明,不同剂量的X射线照射后2小时即出现噬斑形成能力的抑制,6小时时抑制非常严重。在初次或二次反应的任何检测阶段均未观察到敏感性差异。这种急性抑制作用表明,脾脏PFC的维持对辐射高度敏感,并且与照射后相同时间脾脏中[H]胸腺嘧啶核苷摄取严重减少有关。由于先前的研究(哈里斯和佩尔克,1970年)表明,[H]胸腺嘧啶核苷掺入发生在小鼠脾脏的非分裂细胞中,因此得出结论,这种DNA周转对于细胞产生特异性抗体能力的发展很重要,并且X射线辐射对脾脏PFC的急性抑制作用主要是由于该过程的抑制。