吉林大学学报(医学版)

• 基础研究 • 上一篇    下一篇

苯通过激活线粒体凋亡通路对小鼠骨髓细胞凋亡的诱导作用及其机制

于光艳,宋祥福1,赵淑华1,刘晓梅1,孙志伟1,2   


  1. (1.吉林大学公共卫生学院劳动卫生与环境卫生教研室,吉林 长春 130021; 2.首都医科大学公共卫生学院卫生毒理学教研室,北京 100069)
  • 收稿日期:2013-11-09 出版日期:2014-09-28 发布日期:2014-09-28
  • 通讯作者: 孙志伟 E-mail:(Tel:010-83911507,E-mail:zwsun@hotmail.com)
  • 作者简介:于光艳(1976-),女,吉林省吉林市人,讲师,医学博士,主要从事工业及环境毒理学研究。
  • 基金资助:

    国家安监总局计划项目资助课题(08-067);中央高校基本科研业务费专项基金资助课题(450060481119)

Induction effect of benzene on apoptosis of mouse bone marrow cells through mitochondrial-dependent apoptosis pathway and its mechanism

YU Guang-yan1,SONG Xiang-fu1,ZHAO Shu-hua1,LIU Xiao-mei1,SUN Zhi-wei 1,2   

  1. (1.Department of Occupational and Environmental Health,School of Public Health,Jilin University,Changchun 130021,China;2. Department of Hygienic Toxicology,School of Public Health,Capital Medical University,Beijing 100069,China)
  • Received:2013-11-09 Online:2014-09-28 Published:2014-09-28

摘要:

目的:建立小鼠吸入气态苯染毒模型,探讨苯对骨髓细胞凋亡的诱导作用和机制,为苯骨髓毒作用机制的研究提供实验依据。方法:将24只雄性小鼠随机分为对照组和低、中、高剂量苯染毒组(染毒剂量分别为400、800和1 600 mg?m-3),每组6只。各剂量苯染毒组小鼠进行静式染毒,每天2 h,连续染毒15 d后将各组小鼠全部处死,HE染色后光镜下观察各组小鼠骨髓细胞的病理学改变,流式细胞仪测定各组小鼠骨髓细胞凋亡率及线粒体膜电位,免疫组织化学法测定各组小鼠线粒体凋亡途径中相关基因蛋白的表达。结果:低、中和高剂量苯染毒组小鼠骨髓边缘及中央处细胞数明显减少,高剂量苯染毒组小鼠骨髓还伴有大量的血窦扩张。中和高剂量苯染毒组细胞凋亡率明显高于对照组,差异有统计学意义(Ρ<0.01),且高剂量苯染毒组与低和中剂量苯染毒组比较差异也有统计学意义(Ρ<0.05)。低、中和高剂量苯染毒组小鼠骨髓细胞线粒体膜电位随着染毒剂量的增加明显降低,中和高剂量苯染毒组与对照组比较差异有统计学意义(Ρ<0.05或P<0.01)。不同剂量苯染毒组Bax、CytC及中、高剂量苯染毒组Caspases-9、Caspases-3阳性细胞数随染毒剂量的增加显著升高,与对照组比较差异均有统计学意义(Ρ<0.05);而各剂量苯染毒组Bcl-2阳性细胞数则明显低于对照组(Ρ<0.05),且中和高剂量苯染毒组与低剂量苯染毒组比较差异也有统计学意义(Ρ<0.05)。结论:一定剂量的苯可以诱导小鼠骨髓细胞发生凋亡,促进线粒体凋亡相关基因蛋白的表达。通过线粒体凋亡通路诱导的细胞凋亡可能是苯骨髓毒性的重要机制之一。

关键词: 苯, 细胞凋亡, 线粒体膜电位, 凋亡基因蛋白

Abstract:

Abstract:Objective
 To establish mouse poisoning model by inhaling benzene,and to investigate the induction effect of benzene on the apoptosis of mouse bone marrow cells and its mechanism,and to provide an experimental basis for study on bone marrow toxicity mechanism.Methods 24 male mice were randomly divided into four groups (n=6).The mice in one group were exposed to ambient air (control group) and the mice in the other three groups were exposed to different doses (400,800,1 600 mg?m-3) of benzene (low,middle and high doses of benzene groups) for 15 d in the respective inhalation chambers.At the end of the  experiment,the mice were killed.The bone marrow of the mice was obtained.The pathological changes of the bone marrow cells of the mice in various groups were observed under light microscope with HE staining.The apoptotic rates and mitochondrial membrane potential (MMP) of the mice in various groups were detected by flow cytometry, and the expressions of mitochondrial-deperdent apoptosis related gene proteins were determined with immunohistochemistry method.Results The number of distal and central cells in different doses of benzene groups were significantly reduced,and accompanied by blood sinus expansion in high dose of benzene group.The apoptotic rates of the cells in middle and high doses of benzene groups were obviously higher than that in control group (Ρ<0.01),and there were also significant differences between high dose group and low,middle doses of benzene groups (Ρ<0.05).The MMP was significantly decreased with the increasing of benzene doses,and there were significant differences between middle,high doses of benzene groups and control group (Ρ<0.05).The number  of Bax,CytC positive cells in different doses of benzene groups and the number  of Caspase-9,Caspase-3 positive cells in middle and high doses of benzene groups were significantly increased compared with control group(Ρ<0.05);the number of Bcl-2 positive cells in different doses of benzene groups was decreased(Ρ<0.05),and number of Bcl-2 positive cells in middle and high doses of benzene groups was decreased compared with low dose of benzene group(P<0.05).Conclusion Benzene with certain dose can induce the apoptosis of mouse bone marrow cells,and promote the expressions of mitochondrial apoptosis related gene proteins.Benzene-induced apoptosis through mitochondrial-dependent apoptosis pathway may be an important mechanism of bone marrow toxicity induced by benzene.

Key words:  , benzene, apoptosis, mitochondrial membrane potential, apoptosis gene protein

中图分类号: 

  • R114