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作 者:葛柳青[1] 姜挺[1] 赵杰[1] 陈志涛[1] 周峰[1] 夏冰[1]
出 处:《中华消化杂志》2010年第11期811-813,共3页Chinese Journal of Digestion
基 金:国家自然科学基金资助项目(30570834)
摘 要:目的 探讨主要组织相容性复合物Ⅰ类链相关基因(MIC)在溃疡性结肠炎(UC)发病中所起的作用.方法 采用荧光定量实时-聚合酶链反应(RT-PCR)方法检测34例UC患者和17例正常人肠黏膜组织中MICA和MICB及其受体NKG2D mRNA表达水平的差异.采用激光共聚焦显微镜观察肠黏膜组织中MICA分子的表达定位.结果 UC组MICA、MICB及NKG2DmRNA水平的表达量(分别为3.5408±2.6658、8.9879±3.2893和2.4395±0.8147)均显著高于正常对照组(分别为1.0477±0.7201、4.6293±1.2616和1.1624±0.3954,P值分别=0.0053、0.0039和0.0078).免疫荧光共聚焦显微镜观察显示,MICA分子在肠上皮细胞胞膜中表达.结论 UC患者肠黏膜组织中MICA、MICB及其受体NKG2D的mRNA表达水平均增高,提示MIC基.因在UC局部起重要作用.Objective To investigate the function of major histocompatibility complex (MHC)class Ⅰ-related gene (MIC) in ulcerative colitis (UC) pathogenesis. Methods The difference of MICA, M ICB and their ligand NKG2D genes expression in colonic mucosa tissue of 34 UC patients and 12 healthy people were determined by fluorescent real-time reverse-transcriptase polymerase chain reaction (RT-PCR) and the expression location of M ICA in colonic mucosa tissue was obtained by laser scanning confocal microscope. Results The mRNA level of MICA, MICB and NKG2D expression in UC groups (3. 5408±2. 6658, 8. 9879±3. 2893 and 2. 4395±0. 8147 accordingly) was significantly higher than that in the healthy controls ( 1. 0477 ± 0. 7201, 4. 6293 ± 1. 2616 and 1. 1624±0. 3954 accordingly) (P = 0.0053, 0.0039 and 0. 0078 accordingly). It suggested that MICA was expressed in colonic epithelia cell membranes by laser scanning confocal microscopy.Conclusion The mRNA level of MICA, M ICB, and their ligand, NKG2D expression were all up regulated in the colonic mucosa of UC patients, which indicated MIC gene might perform important local function in UC.
关 键 词:结肠炎 溃疡性 基因 主要组织相容性复合物Ⅰ类 NKG2D
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