期刊文献+

微波预先辐照致γ射线对小鼠骨髓基质细胞毒性作用的改变 被引量:1

Pre-exposure with Microwave Alters the Effects of γ-rays on Mouse Bone Marrow Stromal Cells
原文传递
导出
摘要 [目的]探讨微波预先辐照对γ射线致骨髓基质细胞凋亡、线粒体膜电位、胞内游离Ca2+浓度和Ca2+-Mg2+-ATP酶活性改变的影响。[方法]将原代培养的骨髓基质细胞随机分为正常对照组、单纯微波组、单纯γ射线组和联合组。12μW/cm2微波对单纯微波组和联合组连续辐照7d,每天1h,第8天对单纯γ射线组和联合组进行5Gy的γ射线照射。用钙离子依赖性磷脂结合蛋白-异硫氰酸荧光素及碘化丙啶(AnnexinV-FITC及PI)双标记法检测细胞凋亡,流式细胞仪检测线粒体膜电位和胞内游离Ca2+浓度,试剂盒检测Ca2+-Mg2+-ATP酶活性。[结果]与正常对照组相比,各处理组细胞的凋亡率和线粒体膜电位未见明显改变。γ射线照射后24h,单纯微波组、联合组和单纯γ射线组细胞内游离Ca2+浓度明显升高(P<0.05),Ca2+-Mg2+-ATP酶活性明显降低(P<0.05)。与单纯γ射线组相比,联合组细胞内游离Ca2+浓度明显降低(P<0.05),Ca2+-Mg2+-ATP酶活性明显升高(P<0.05)。[结论]本实验条件下,900MHz,12μW/cm2的微波辐射和5Gyγ射线均不能引起细胞凋亡率、线粒体膜电位的明显变化,但能导致胞内游离Ca2+浓度明显上升和Ca2+-Mg2+-ATP酶活性明显降低。预先微波辐照能够明显减弱γ射线引起的胞内游离Ca2+浓度和Ca2+-Mg2+-ATP酶活性改变。 [ Objective ] To explore the effects of pre-exposure with microwave on y-rays induced apoptosis, mitochondrion membrane potential ( MMP ), intracellular Ca^2+ concentration and Ca^2+-Mg^2+-ATPase activity in mouse bone marrow stromal cells. [ Methods ] Primarily cultured mouse bone marrow stromal cells were randomly divided into control group, microwave alone group, T-rays group and combined exposure group. The microwave alone and combined exposure groups were exposed to 12 μW/cm^2 microwave I h a day for 7 days. The T-rays alone and combined exposure groups were subsequently exposed to 5 Gy ^60Co T-rays on the 8th day. Ca^2+ concentration and MMP were detected by a flow cytometry( FCM ). Apoptosis was detected by Annexin V-FITC/PI, and Ca^2+-Mg^2+-ATPase activities were analyzed by a commercial kit. [ Results ] There were no significantly differences between different groups in apoptosis and MMP. 24 h after y-rays irradiation, the Ca^2+ concentrations of the microwave alone, the y-rays alone and the combined exposure groups were statistically higher than those of the control group( P〈0.05 ), while Ca^2+-Mg^2+-ATPase activities were statistically lower than those of the control group( P〈0.05 ). Compared with the T-rays alone group, Ca2. concentrations of the combined exposure group significantly decreased ( P 〈 0.05 ) and Ca^2+-Mg^2+-ATPase activity statistically increased ( P 〈 0.05 ). [ Conclusion ] Under the experimental condition, microwave radiation (900 MHz, 12 μW/cm^2) and 5 Gy γ-rays did not induce evident changes in apoptosis and MMP; but did induce an increase of Ca^2+ concentrations and a decrease of Ca^2+-Mg^2+-ATPase activity. Pre-exposure with microwave could significantly decrease T-rays induced changes in Ca^2+ concentration and Ca^2+-Mg^2+-ATPase activity.
出处 《环境与职业医学》 CAS 北大核心 2011年第1期35-38,42,共5页 Journal of Environmental and Occupational Medicine
基金 江苏省放射医学与防护重点实验室开放课题(编号:KJS0930)
关键词 微波 Γ射线 凋亡 线粒体膜电位 Ca^2+ CA^2+ Mg^2+-ATP酶 microwave v-rays apoptosis MMP Ca^2+ Ca^2+-Mg^2+-ATPase
  • 相关文献

参考文献16

二级参考文献70

共引文献70

同被引文献18

  • 1孟谦谦,周智钿,童建,曹毅.微波和电离辐射对小鼠联合作用的研究[J].苏州大学学报(医学版),2007,27(3):344-346. 被引量:9
  • 2Cao Y, Xu Q, Jin Z D, et al. Effects of 900 MHz microwave radiation on gamma-ray induced damage to mouse hematopoietic system [J]. J Toxicol Environ Health, 2010, 73(7): 507-513.
  • 3Jiang B, Nie J, Zhou Z, et al. Adaptive response in mice exposed to 900 MHz radiofrequency fields: Primary DNA damage[J]. PLoS One, 2012, 7( 2 ): e32040.
  • 4Cao Y, Xu Q, Jin Z D, et al. Induction of adaptive response: Pre-exposure of mice to 900 MHz radiofrequency fields reduces hematopoietic damage caused by subsequent exposure to ionising radiation[J]. Int J Radiat Biol, 2011, 87( 7 ): 720-728.
  • 5Sannino A, Zeni O, Sarti M, et al. Induction of adaptive response in human blood lymphocytes exposed to 900 MHz radiofrequency fields : Influence of cell cycle [J]. Int J Radiat Biol, 2011, 87(9): 993-999.
  • 6Vijayalaxmi, Burkart W. Effect of 3-aminobenzamide on chromosome damage in human blood lymphocytes adapted to bleomyein[J]. Mutagenesis, 1989, 4( 3 ): 187-189.
  • 7Xu S, Zhou Z, Zhang L, et al. Exposure to 1800 MHz radiofrequeney radiation induces oxidative damage to mitochondrial DNA in primary cultured neurons [J]. Brain Res, 2010, 1311: 189-196.
  • 8Singh N P, McCoy M T, Tice R R, et al. A simple technique for quantitation of low levels of DNA damage in individual ceils [J]. Exp Cell Res, 1988, 175( 1 ): 184-191.
  • 9Skalka A M, Katz R A. Retroviral DNA integration and the DNA damage response [J]. Cell Death Differ, 2005, 12 ( Suppl 1 ): 971-978.
  • 10Paull TT, Rogakou EP, Yamazaki V, et al. A critical role forhistone H2AX in recruitment of repair factors to nuclear oci after DNA damage[J]. Curr Biol, 2000, 10( 15 ): 886-895.

引证文献1

二级引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部