Departments of Pediatrics and Neonatology, University of Rochester Medical Center, Rochester, New York 14642, USA.
Radiat Res. 2010 Apr;173(4):522-35. doi: 10.1667/RR1882.1.
To assess early changes in the lung after low-dose radiation exposure that may serve as targets for mitigation of lung injury in the aftermath of a terrorist event, we analyzed cytokine expression after irradiation. Adult mice were studied after whole-lung or total-body irradiation. Mouse pups of different ages were also investigated after total-body irradiation. mRNA abundance was analyzed in tissue and plasma, and pathological changes were assessed. In lung tissue, dose-related changes were seen in IL1B, IL1R2 and CXCR2 mRNA expression at 1 and 6 h after irradiation, concurrent with increases in plasma protein levels of KC/CXCL1 and IL6. However, in the pups, changes in IL1 abundance were not detected until 28 days of age, coincident with the end of postnatal lung growth, although apoptosis was detected at all ages. In conclusion, although cytokines were expressed after low doses of radiation, their role in the progression of tissue response is yet to be determined. They may be candidates for use in marker-based biodosimetry. However, the lack of cytokine induction in early life suggests that different end points (and mitigating treatments) may be required for children.
为了评估低剂量辐射后肺部的早期变化,这些变化可能成为减轻恐怖事件后肺损伤的目标,我们分析了照射后的细胞因子表达。研究了全肺或全身照射后的成年小鼠,以及全身照射后的不同年龄的幼鼠。分析了组织和血浆中的 mRNA 丰度,并评估了病理变化。在肺组织中,照射后 1 和 6 小时,IL1B、IL1R2 和 CXCR2 mRNA 表达与 KC/CXCL1 和 IL6 的血浆蛋白水平增加呈剂量相关性变化。然而,在幼鼠中,直到 28 天龄时才检测到 IL1 丰度的变化,这与出生后肺生长结束时间一致,尽管在所有年龄都检测到了细胞凋亡。总之,尽管在低剂量辐射后表达了细胞因子,但它们在组织反应进展中的作用仍有待确定。它们可能是基于标志物的生物剂量测定的候选物。然而,在生命早期缺乏细胞因子诱导表明,儿童可能需要不同的终点(和缓解治疗)。