Modulation of in vitro cytokine release from human leukemic mast cells (HMC-1) by glucocorticoids.

U Lippert, P Welker, S Krüger-Krasagakes, A Möller, B M Henz
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引用次数: 16

Abstract

Mast cells are well known effector cells not only in allergic but also in diverse acute and chronic inflammatory diseases. We have shown previously that these cells produce a broad spectrum of cytokines which might contribute to mast cell-dependent pathology. In the present study, we have investigated the influence of four potent glucocorticoids, methylprednisolone-aceponate, methylprednisolone-17-propionate, prednicarbate, and betametasone valerate (10(-5) M-10(-9) M), on the IL-1 beta, IL-3, IL-8, and tumor necrosis factor alpha secretion of the HMC-1 mast cell line as measured by ELISA. All four glucocorticoids caused a comparable dose- and time-dependent inhibition of cytokine release from HMC-1 cells stimulated for 24 h with phorbol 12-myristate 13-acetate 25 ng/ml and calcium ionophore 2 x 10(-7) M. These results shed further light on the mechanisms involved in antiinflammatory effects of glucocorticoids in allergic inflammation.

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糖皮质激素对人白血病肥大细胞(HMC-1)体外细胞因子释放的调节
肥大细胞是一种众所周知的效应细胞,不仅在过敏性疾病中,而且在各种急慢性炎症疾病中都有作用。我们以前已经表明,这些细胞产生广泛的细胞因子,这可能有助于肥大细胞依赖性病理。在本研究中,我们研究了四种有效的糖皮质激素,甲基强的松龙-乙酰酸酯、甲基强的松龙-17-丙酸酯、泼尼卡巴酯和戊酸倍他米松(10(-5)M-10(-9) M)对HMC-1肥大细胞系IL-1 β、IL-3、IL-8和肿瘤坏死因子α分泌的影响。所有四种糖皮质激素对HMC-1细胞释放的剂量和时间依赖性抑制作用相当,12-肉豆蔻酸13-醋酸酯25 ng/ml和钙离子载体2 × 10(-7) m刺激24小时。这些结果进一步阐明了糖皮质激素在过敏性炎症中的抗炎作用机制。
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