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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
钟万锷1,周国雄1*,丁晓凌1,黄华2
0
(1.南通大学附属医院消化内科,南通 226001;2.南通大学附属医院病理科,南通 226001)
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。
关键词:  溃疡性结肠炎  巨噬细胞炎症蛋白-3α  CCR6受体
DOI:10.3724/SP.J.1008.2008.00
投稿时间:2008-01-26修订日期:2008-03-27
基金项目:
Expression of chemokine MIP-3α and its receptor CCR6 in ulcerative colitis and its significance
ZHONG Wan-e1, ZHOU Guo-xiong1*,DING Xiao-ling1,HUANG Hua2
(1. Department of Gastroenterology, Affiliated Hospital of Nantong University, Nantong 226001, China;2. Department of Pathology, Affiliated Hospital of Nantong University, Nantong 226001)
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.
Key words:  ulcerative colitis  macrophage inflammatory protein-3α  CCR6 receptors