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首页> 外文期刊>Radiation and Environmental Biophysics >Production of cytokines by peritoneal macrophages and splenocytes after exposures of mice to low doses of X-rays
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Production of cytokines by peritoneal macrophages and splenocytes after exposures of mice to low doses of X-rays

机译:小鼠暴露于低剂量的X射线后,腹膜巨噬细胞和脾细胞产生细胞因子

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We have shown previously that irradiations of mice with 0.1 or 0.2 Gy of X-rays stimulate anti-tumour cytotoxic activities of peritoneal macrophages and spleno-cytes enriched for NK lymphocytes and suppress the development of pulmonary tumour colonies.The up-regulated cytotoxicities were related to the production of nitric oxide by macrophages,and perforin and Fas ligand by the spleno-cytes,but specific blockade of these pathways did not totally suppress the effector cell-mediated cytolysis of the tumour target.Hence,other factors such as cytotoxic/cytostatic cytokines might have been produced by the effector cells.To test this possibility peritoneal macrophages and splenocytes were isolated from BALB/c mice which had been either once or tentimes whole body-irradiated with the total doses of 0.1 and 0.2 Gy of X-rays and assayed for the levels of IL-1beta,IL-2,IL-12,IFN-gamma and TNF-alpha in the incubation medium using the respective ELISA kits.The results demonstrate that both single and multiple exposures to the two low doses of X-rays significantly stimulate secretion of IL-1beta,TNF-alpha and IL-12 by macrophages and IL-2 and IFN-gamma by splenocytes,but the kinetics and magnitude of the induced changes in the production of these cytokines differ between the two irradiation protocols.
机译:先前我们已经证明,用0.1或0.2 Gy的X射线照射小鼠可刺激腹膜巨噬细胞和富含NK淋巴细胞的脾细胞的抗肿瘤细胞毒性活性,并抑制肺肿瘤菌落的发展。与细胞毒性上调有关对巨噬细胞产生一氧化氮,脾细胞产生穿孔素和Fas配体产生抑制作用,但这些途径的特异性阻断并不能完全抑制效应细胞介导的肿瘤靶标细胞溶解。因此,其他因素如细胞毒性/抑制细胞生长为了检验这种可能性,为了检验这种可能性,从BALB / c小鼠中分离了腹膜巨噬细胞和脾细胞,对它们进行了一次或十次全身照射,总剂量为0.1和0.2 Gy的X射线和使用相应的ELISA试剂盒检测培养液中IL-1beta,IL-2,IL-12,IFN-γ和TNF-α的水平。并多次暴露于两种低剂量的X射线可显着刺激巨噬细胞分泌IL-1beta,TNF-α和IL-12,并刺激脾细胞分泌IL-2和IFN-γ,但诱导的动力学和变化幅度这些细胞因子的产生在两种照射方案之间是不同的。

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