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溃疡性结肠炎中细胞因子的研究。

Study of cytokines in ulcerative colitis.

作者信息

Funakoshi K, Sugimura K, Sasakawa T, Bannai H, Anezaki K, Ishizuka K, Yoshida K, Narisawa R, Asakura H

机构信息

Third Department of Internal Medicine, Niigata University, School of Medicine, Japan.

出版信息

J Gastroenterol. 1995 Nov;30 Suppl 8:61-3.

PMID:8563893
Abstract

We investigated the lymphocyte-activation antigens and the expression of cytokine genes in the mucosa of ulcerative colitis (UC). Fresh colonic mucosal biopsy specimens from patients with UC and controls were fixed for the immunohistochemical study of CD4, HLA-DR, and CD25, and other specimens were prepared for the RNA analysis of cytokines. Gene expression was evaluated by the reverse transcription-polymerase chain reaction, and the radioactivity of dot-blotted amplified cDNA was standardized by co-amplified beta-actin cDNA. The inflamed mucosa of active UC showed increased CD4+DR+ and CD25+ cells in comparison with control subjects. Active UC showed significantly increased mRNA expression of IL-1 beta, IL-2R alpha, IL-6, IL-8, and TNF alpha compared with the controls. We found no significant difference in the mRNA expression for IL-2, IL-4, IL-10, and IFN-gamma between active UC and controls. Increased CD4+DR+ and CD25+ cells in active UC mucosa indicate mucosal CD4(+) T cell activation in the lamina propria, but we did not clarify Th1 or Th2 specific T cell activation from our study of cytokine mRNA expression. The increased mRNA expression for IL-1 beta, IL-6, and TNF alpha in the mucosal lesions of UC indicates that these inflammatory cytokines may play important roles in the pathogenesis of UC.

摘要

我们研究了溃疡性结肠炎(UC)黏膜中的淋巴细胞激活抗原及细胞因子基因表达。取自UC患者和对照者的新鲜结肠黏膜活检标本用于CD4、HLA - DR和CD25的免疫组织化学研究,其他标本则用于细胞因子的RNA分析。通过逆转录 - 聚合酶链反应评估基因表达,并通过共扩增的β - 肌动蛋白cDNA对斑点印迹扩增cDNA的放射性进行标准化。与对照受试者相比,活动期UC的炎症黏膜中CD4 + DR +和CD25 +细胞增多。与对照相比,活动期UC的IL - 1β、IL - 2Rα、IL - 6、IL - 8和TNFα的mRNA表达显著增加。我们发现活动期UC与对照之间IL - 2、IL - 4、IL - 10和IFN - γ的mRNA表达无显著差异。活动期UC黏膜中CD4 + DR +和CD25 +细胞增多表明固有层中黏膜CD4(+)T细胞激活,但我们通过细胞因子mRNA表达研究未明确Th1或Th2特异性T细胞激活情况。UC黏膜病变中IL - 1β、IL - 6和TNFα的mRNA表达增加表明这些炎性细胞因子可能在UC发病机制中起重要作用。

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