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机构地区:[1]武汉市中心医院消化内科,湖北省武汉市430014 [2]武汉大学中南医院内科与病理科,湖北省武汉市430071 [3]武汉大学医学院消化系病研究中心,湖北省武汉市430071 [4]武汉大学医学院过敏与免疫相关疾病研究中心,湖北省武汉市430071
出 处:《世界华人消化杂志》2006年第18期1795-1798,共4页World Chinese Journal of Digestology
摘 要:目的:研究溃疡性结肠炎(UC)肠黏膜CD8 T细胞Fas/FasL、Bcl-2/Bax蛋白表达以及相互关系,探讨细胞凋亡机制在UC发病中的作用.方法:采用免疫组化SP法检测60例UC肠黏膜组织以及60例正常肠黏膜组织CD8,Fas/FasL, Bcl-2/Bax蛋白表达.结果:CD8阳性细胞在上皮间的浸润在UC 组为52%,正常组为78%,两组相比差异显著 (P<0.01);急性期较缓解期也显著减少(20% vs 74%,P<0.01).CD8在UC患者急性期黏膜固有层的表达为80%,高于缓解期的34%(P= 0.0006).Fas在UC上皮中表达62%,正常组织 30%,两组相比差异显著(P<0.01);急性期高于缓解期(84% vs 45%,P<0.01).FasL在固有膜炎性细胞中的表达UC组为62%,正常组7%, 两组相比差异显著(P<0.00;急性期(88%)高于缓解期(43%),而且CD8与FasL在黏膜固有层炎性细胞的表达呈正相关(X2=7.3,P<0.01). Bcl-2/Bax在UC肠黏膜上皮的表达率与正常组相近,差异无显著性.结论:UC肠黏膜组织Fas/FasL表达增强, Bcl-2/Bax表达无明显变化,CD8细胞与UC急性期Fas/FasL表达相关.AIM: To investigate the expression of Fas/FasL and Bcl-2/Bax and distribution of CD8 T cells as well as their correlations in ulcerative colitis (UC), METHODS: Immunohistochemistry was used to detect the expression of CD8, Bcl-2/Bax and Fas/FasL in intestinal mucosal tissues from UC (n = 60) and normal controls (n = 60), RESULTS: The positive rate of CD8 was significantly higher in the epithelia of UC tissues than that in the controls (52% vs 78%, P 〈 0.01), and rate in the active UC was also significantly lower than that in the remissive UC (20% vs 74%, P 〈 0,01). The positive rate of CD8 in the lamina propria tissues of UC at active stage was markedly higher than that at rernissive stage (80% vs 34%,P = 0.0006). The expression of Fas was remarkably higher in the epithelia of UC tissues than that in the controls (62% vs 30%, P 〈 0.01), and its expression at active UC was also dramatically higher than that at remissive stage (84% vs 45%, P 〈 0.01). The expression of FasL was significantly increased in the inflammatory cells from the lamina propria of UC tissues as compared with that from normal mucosa (62% vs 7%, P 〈 0.01), and it was also a significant different between the active and remissive stage (88% vs 43%, P 〈 0.01). Furthermore, there was a correlation between the expression CD8 and FasL in the inflammatory cells from the lamina propria (χ^2 = 7.3, P 〈 0.01). The expression of Bcl-2/Bax was not different between UC and normal mucosa (P 〉 0.05). CONCLUSION: The expression of Fas/FasL is up-regulated in UC, but the expression of Bcl-2/ Bax is not obviously changed. CD8 T cells play important roles in the development of UC and they are closely related with Fas/FasL system.
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