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白细胞介素-3、白细胞介素-5和粒细胞-巨噬细胞集落刺激因子可增强嗜酸性粒细胞颗粒主要碱性蛋白刺激的嗜碱性粒细胞介质释放。

IL-3, IL-5, and granulocyte-macrophage colony-stimulating factor potentiate basophil mediator release stimulated by eosinophil granule major basic protein.

作者信息

Sarmiento E U, Espiritu B R, Gleich G J, Thomas L L

机构信息

Department of Immunology/Microbiology, Rush Medical College, Chicago, IL 60612, USA.

出版信息

J Immunol. 1995 Aug 15;155(4):2211-21.

PMID:7543541
Abstract

We have examined the potential of IL-3, IL-5, and granulocyte-macrophage (GM)-CSF to enhance basophil activation by eosinophil granule major basic protein (MBP). Preincubating basophil-containing mononuclear cells with 0.01 to 10 ng/ml IL-3 or IL-5 for 15 min at 37 degrees C caused a concentration-dependent enhancement of histamine release stimulated by 1.5 microM MBP. Statistically significant enhancement was evident at 1 ng/ml and was maximal at 10 ng/ml. Preincubation with GM-CSF similarly enhanced MBP-induced histamine release. A 10- to 15-min preincubation with IL-5 maximally increased the level of MBP-stimulated histamine release. Preincubation of cells with 10 ng/ml IL-3 or IL-5 reduced the MBP concentrations required for histamine release by three- to fourfold and enhanced the rate of MBP-induced histamine release. MBP-stimulated histamine release before or after cytokine priming was independent of cytotoxicity as measured by 51Cr release. Consistent with a direct action of the cytokines on basophils, flow cytometric analysis demonstrated the presence of IL-3 and GM-CSF receptors on basophils. MBP also stimulated low levels of leukotriene C4 (LTC4) release from basophils of 84 to 99% purity, and experiments using enriched (18-63%) basophil preparations demonstrated that preincubation with IL-3, IL-5, and GM-CSF also potentiated MBP-stimulated leukotriene C4 release up to threefold in parallel with histamine release. These results indicate that IL-3, IL-5, and GM-CSF may contribute to the pathogenesis of allergic and other disorders characterized by eosinophilia in part through potentiation of basophil mediator release stimulated by MBP.

摘要

我们研究了白细胞介素-3(IL-3)、白细胞介素-5(IL-5)和粒细胞-巨噬细胞集落刺激因子(GM-CSF)增强嗜酸性粒细胞颗粒主要碱性蛋白(MBP)激活嗜碱性粒细胞的潜力。将含嗜碱性粒细胞的单核细胞与0.01至10 ng/ml的IL-3或IL-5在37℃预孵育15分钟,导致1.5 microM MBP刺激的组胺释放呈浓度依赖性增强。在1 ng/ml时,统计学上显著增强,在10 ng/ml时达到最大值。与GM-CSF预孵育同样增强了MBP诱导的组胺释放。与IL-5预孵育10至15分钟可最大程度地提高MBP刺激的组胺释放水平。用10 ng/ml的IL-3或IL-5预孵育细胞可将组胺释放所需的MBP浓度降低三至四倍,并提高MBP诱导的组胺释放速率。细胞因子引发前后MBP刺激的组胺释放与通过51Cr释放测量的细胞毒性无关。与细胞因子对嗜碱性粒细胞的直接作用一致,流式细胞术分析表明嗜碱性粒细胞上存在IL-3和GM-CSF受体。MBP还刺激了纯度为84%至99%的嗜碱性粒细胞释放低水平的白三烯C4(LTC4),并且使用富集(18% - 63%)嗜碱性粒细胞制剂的实验表明,与组胺释放平行,用IL-3、IL-5和GM-CSF预孵育也可使MBP刺激的白三烯C4释放增强至三倍。这些结果表明,IL-3、IL-5和GM-CSF可能部分通过增强MBP刺激的嗜碱性粒细胞介质释放,在以嗜酸性粒细胞增多为特征的过敏性和其他疾病的发病机制中起作用。

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