Radiation Countermeasures Program, Armed Forces Radiobiology Research Institute, Bethesda, MD 20889-5603, USA.
Cytokine. 2011 Nov;56(2):411-21. doi: 10.1016/j.cyto.2011.08.016. Epub 2011 Aug 30.
The purpose of this study was to elucidate the role of granulocyte colony-stimulating factor (G-CSF) induced by α-tocopherol succinate (TS) in protecting mice from total-body irradiation. CD2F1 mice were injected with a radioprotective dose of TS and the levels of cytokine in serum induced by TS were determined by multiplex Luminex. Neutralization of G-CSF was accomplished by administration of a G-CSF antibody and confirmed by cytokine analysis. The role of G-CSF on gastrointestinal tissue protection afforded by TS after irradiation (11 Gy, 0.6 Gy/min of 60Co γ-radiation) was determined by analysis of jejunum histopathology for crypt, villi, mitotic figures, apoptosis, and cell proliferation. Our results demonstrate that TS protected mice against high doses of radiation-induced gastrointestinal damage and TS also induced very high levels of G-CSF and keratinocyte-derived chemokine (KC) production in peripheral blood 24 h after subcutaneous administration. When TS-injected mice were administered a neutralizing antibody to G-CSF, there was complete neutralization of G-CSF in circulating blood, and the protective effect of TS was significantly abrogated by G-CSF antibody. Histopathology of jejunum from TS-injected and irradiated mice demonstrated protection of gastrointestinal tissue, yet the protection was abrogated by administration of a G-CSF antibody. In conclusion, our current study suggests that induction of G-CSF resulting from TS administration is responsible for protection from 60Co γ-radiation injury.
本研究旨在阐明α-生育酚琥珀酸酯(TS)诱导的粒细胞集落刺激因子(G-CSF)在保护小鼠免受全身辐射中的作用。用放射保护剂量的 TS 注射 CD2F1 小鼠,并通过多重 Luminex 测定 TS 诱导的血清细胞因子水平。通过给予 G-CSF 抗体中和 G-CSF,并通过细胞因子分析进行确认。通过分析照射后(11 Gy,60Co γ 射线 0.6 Gy/min)TS 对胃肠道组织的保护作用,确定 G-CSF 在 TS 中的作用。用绒毛、有丝分裂、凋亡和细胞增殖分析空肠组织病理学。我们的结果表明,TS 可保护小鼠免受高剂量辐射引起的胃肠道损伤,并且在皮下给予 TS 后 24 小时,外周血中也诱导了非常高水平的 G-CSF 和角质细胞衍生的趋化因子(KC)产生。当给予 TS 注射小鼠中和 G-CSF 的抗体时,循环血液中的 G-CSF 完全中和,G-CSF 抗体显著削弱了 TS 的保护作用。TS 注射和照射小鼠的空肠组织病理学表明胃肠道组织得到保护,但给予 G-CSF 抗体后保护作用被消除。总之,我们目前的研究表明,TS 给药诱导的 G-CSF 是对 60Co γ 射线损伤的保护作用的原因。