趋化因子MIP-3α及其受体CCR6在溃疡性结肠炎中的表达及其意义
CSTR:
作者:
作者单位:

作者简介:

通讯作者:

中图分类号:

基金项目:


Expression of chemokine MIP-3α and its receptor CCR6 in ulcerative colitis and its significance
Author:
Affiliation:

Fund Project:

  • 摘要
  • |
  • 图/表
  • |
  • 访问统计
  • |
  • 参考文献
  • |
  • 相似文献
  • |
  • 引证文献
  • |
  • 资源附件
  • |
  • 文章评论
    摘要:

    目的:研究趋化因子巨噬细胞炎症蛋白-3α(MIP-3α)及其受体CCR6在溃疡性结肠炎(UC)中的表达情况以及与UC病变程度和范围的关系,探讨其在UC发病机制中的作用。方法:用免疫组织化学法检测35例活动期UC及20例正常对照石蜡包埋组织中MIP-3α及CCR6的表达情况。结果:UC组MIP-3α及CCR6均为阳性表达,对照组为阴性或弱阳性表达。MIP-3α及CCR6在UC组的表达与对照组相比,差异有统计学意义(P<0.01)。UC病变范围越广、程度越重,MIP-3α及CCR6表达阳性率越高;且MIP-3α和CCR6表达有明显相关性(r=0.765,P<0.01)。 结论:MIP-3α与CCR6均参与了UC的发生和发展,两者的相互作用可能在UC局部结肠组织破坏和病理变化中起着重要作用。

    Abstract:

    Objective:To investigate the expression of chemokine MIP-3α and its receptor CCR6 in ulcerative colitis(UC) and to explore its relationship with the involvement and severity of UC,so as to asses their expression in the pathogenesis of UC.Methods:The expression of MIP-3α and CCR6 protein in the colon mucosa was detected by immunohistochemistry method in 35 UC patients and 20 normal controls.Results:MIP-3α and CCR6 were both positive in the UC group and negative or only weakly expressed in the normal control group. The expression of MIP-3α and CCR6 in the UC group was significantly higher than that in normal controls (P<0.01). The expression of MIP-3α and CCR6 was related to the severity and involvement of UC. The expression of MIP-3α was significantly correlated with that of CCR6(r=0.765,P<0.01).Conclusion: The expression of MIP-3α and CCR6 is positively correlated with each other, and both of them participate in the development and progression of UC. The interaction between the 2 may play an important role in the local damage and pathological changes in UC.

    参考文献
    相似文献
    引证文献
相关视频

分享
文章指标
  • 点击次数:
  • 下载次数:
  • HTML阅读次数:
  • 引用次数:
历史
  • 收稿日期:2008-01-26
  • 最后修改日期:2008-03-27
  • 录用日期:2008-07-17
  • 在线发布日期: 2008-10-08
  • 出版日期:
文章二维码
重要通知
友情提醒: 近日发现论文正式见刊或网络首发后,有人冒充我刊编辑部名义给作者发邮件,要求添加微信,此系诈骗行为!可致电编辑部核实:021-81870792。
            《海军军医大学学报》编辑部
关闭