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一种哮喘中支气管上皮细胞衍生的因子,其促进嗜酸性粒细胞活化和存活的作用与粒细胞-巨噬细胞集落刺激因子相同。

A bronchial epithelial cell-derived factor in asthma that promotes eosinophil activation and survival as GM-CSF.

作者信息

Soloperto M, Mattoso V L, Fasoli A, Mattoli S

机构信息

Department of Respiratory Disease, School of Medicine, University of Milan, Italy.

出版信息

Am J Physiol. 1991 Jun;260(6 Pt 1):L530-8. doi: 10.1152/ajplung.1991.260.6.L530.

Abstract

We have examined the in vitro interaction between bronchial epithelial cells and eosinophils derived from five asthmatics by determining the effect of epithelial cell-conditioned medium on the survival and activation of peripheral blood eosinophils. The supernatants of epithelial cells from six normal donors were used as control. The asthmatic epithelial cell-conditioned medium significantly increased the survival of eosinophils cultured for 3 (P less than 0.025) and 6 (P less than 0.05) days. The incubation of eosinophils with the supernatants of asthmatic epithelial cells for 1 h also increased the generation of superoxide anion and the release of leukotriene C4, triggered by phorbol myristate acetate and calcium ionophore, by more than twofold. The preincubation of asthmatic epithelial cell-conditioned media with saturating concentrations of a mono-specific antiserum against granulocyte-macrophage colony-stimulating factor (GM-CSF) completely abolished their activity, whereas the addition of recombinant human GM-CSF restored it. The supernatants of asthmatic epithelial cells contained 0.88 +/- 0.09 (SD) ng/5 X 10(5) cells immunoreactive GM-CSF, and this amount was significantly greater than that measured in the supernatants of normal epithelial cells (0.21 +/- 0.105, P less than 0.025). Bronchial epithelial cells from asthmatics also expressed increased levels of GM-CSF mRNA when compared with normal epithelial cells. Thus both the synthesis and release of GM-CSF by bronchial epithelial cells are upregulated in asthma, and this may contribute to the persistence of eosinophil infiltration and activation in asthmatic airways.

摘要

我们通过测定支气管上皮细胞条件培养基对外周血嗜酸性粒细胞存活和激活的影响,研究了来自五名哮喘患者的支气管上皮细胞与嗜酸性粒细胞之间的体外相互作用。来自六名正常供体的上皮细胞上清液用作对照。哮喘患者上皮细胞条件培养基显著提高了培养3天(P<0.025)和6天(P<0.05)的嗜酸性粒细胞的存活率。将嗜酸性粒细胞与哮喘患者上皮细胞的上清液孵育1小时,也使佛波酯肉豆蔻酸酯和钙离子载体引发的超氧阴离子生成和白三烯C4释放增加了两倍多。用饱和浓度的抗粒细胞-巨噬细胞集落刺激因子(GM-CSF)单特异性抗血清预孵育哮喘患者上皮细胞条件培养基完全消除了它们的活性,而添加重组人GM-CSF可恢复其活性。哮喘患者上皮细胞的上清液含有0.88±0.09(SD)ng/5×10⁵个细胞的免疫反应性GM-CSF,这个量显著高于正常上皮细胞上清液中测得的量(0.21±0.105,P<0.025)。与正常上皮细胞相比,哮喘患者的支气管上皮细胞GM-CSF mRNA表达水平也增加。因此,哮喘时支气管上皮细胞GM-CSF的合成和释放均上调,这可能有助于哮喘气道中嗜酸性粒细胞浸润和激活的持续存在。

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