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首页> 外文期刊>World Journal of Gastroenterology >Induction of tryptase and histamine release from human colon mast cells by IgE dependent or independent mechanisms
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Induction of tryptase and histamine release from human colon mast cells by IgE dependent or independent mechanisms

机译:通过IgE依赖或独立机制诱导人结肠肥大细胞释放类胰蛋白酶和组胺

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摘要

AIM: To investigate the tryptase and histamine release ability of human colon mast cells upon IgE dependent or independent activation and the potential mechanisms. METHODS: Enzymatically dispersed cells from human colons were challenged with anti-IgE or calcium ionophore A23187, and the cell supernatants after challenge were collected. Both concentration dependent and time course studies with anti-IgE or calcium ionophore A23187 were performed. Tryptase release was determined with a sandwich ELISA procedure and histamine release was measured using a glass fibre-based fluorometric assay. RESULTS: Both anti-IgE and calcium ionophore were able to induce dose dependent release of histamine from colon mast cells with up to approximately 60% and 25% net histamine release being achieved with 1 μg/mL calcium ionophore and 10 μg/mL anti-IgE, respectively. Dose dependent release of tryptase was also observed with up to approximately 19 ng/mL and 21 ng/mL release of tryptase being achieved with 10 μg/mL anti-IgE and 1 μg/ mL calcium ionophore, respectively. Time course study revealed that both tryptase and histamine release from colon mast cells stimulated by anti-IgE initiated within 10 sec and reached their maximum release at 6 min following challenge. Pretreatment of cells with metabolic inhibitors abolished the actions of anti-IgE as well as calcium ionophore. Tryptase and histamine release, particularly that induced by calcium ionophore was inhibited by pretreatment of cells with pertussis toxin. CONCLUSION: Both anti-IgE and calcium ionophore are able to induce significant release of tryptase and histamine from colon mast cells, indicating that this cell type is likely to contribute to the pathogenesis of colitis and other mast cell associated intestinal diseases.
机译:目的:研究人结肠肥大细胞依赖IgE或独立激活后类胰蛋白酶和组胺的释放能力及其潜在机制。方法:用抗IgE或钙离子载体A23187攻击人结肠中酶分散的细胞,收集攻击后的细胞上清液。使用抗IgE或钙离子载体A23187进行了浓度依赖性研究和时程研究。用三明治ELISA程序确定类胰蛋白酶的释放,并使用基于玻璃纤维的荧光测定法测量组胺的释放。结果:抗IgE和钙离子载体都能诱导结肠肥大细胞中剂量依赖性的组胺释放,其中1μg/ mL钙离子载体和10μg/ mL的抗IgE可以达到约60%和25%的净组胺净释放。 IgE。还观察到了胰蛋白酶的剂量依赖性释放,分别用10μg/ mL抗IgE和1μg/ mL钙离子载体实现了高达约19 ng / mL和21 ng / mL的胰蛋白酶的释放。时程研究显示,抗IgE刺激的结肠肥大细胞中的类胰蛋白酶和组胺释放均在10秒内开始,并在攻击后6分钟达到最大释放。用代谢抑制剂预处理细胞可消除抗IgE和钙离子载体的作用。用百日咳毒素预处理细胞可抑制类胰蛋白酶和组胺的释放,特别是钙离子载体诱导的释放。结论:抗IgE和钙离子载体都能够诱导结肠肥大细胞大量释放类胰蛋白酶和组胺,表明该细胞类型可能与结肠炎及其他肥大细胞相关的肠道疾病的发病机理有关。

著录项

  • 来源
    《World Journal of Gastroenterology 》 |2004年第3期| p.319-322| 共4页
  • 作者单位

    Allergy and Inflammation Research Institute, Shantou University Medical College, 22 Xin-Ling Road, Shantou 515031, Guangdong Province, China;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 消化系及腹部疾病 ;
  • 关键词

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