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人重组白细胞介素-5对豚鼠嗜酸性粒细胞的激活作用。对血小板活化因子-乙醚的选择性致敏作用及其拮抗剂的干扰作用。

Activation of guinea pig eosinophils by human recombinant IL-5. Selective priming to platelet-activating factor-acether and interference of its antagonists.

作者信息

Coëffier E, Joseph D, Vargaftig B B

机构信息

Unité de Pharmacologie Cellulaire, Unité Associée Institut Pasteur-INSERM no. 285, Paris, France.

出版信息

J Immunol. 1991 Oct 15;147(8):2595-602.

PMID:1655895
Abstract

The potential role of platelet-activating factor (PAF)-acether and of IL-5 as an eosinophil-proliferating, activating, and/or recruiting mediator in asthma led us to study the effects of human (h) rIL-5 (hrIL-5) and PAF-acether, alone or combined, on isolated guinea pig eosinophils. Two populations of eosinophils were separated from peritoneal lavages of polymyxin B-treated guinea pigs upon a discontinuous metrizamide gradient: one of low density (between 20 and 22% of metrizamide, purity: 63 +/- 3%, n = 27) and another of normal density (between 22 and 24% of metrizamide, purity: 87 +/- 2%, n = 16). Chemotactic activity was evaluated on a micro-Boyden chamber, results being expressed as the number of migrating eosinophils (mean +/- SEM) at 40 microns through a cellulose nitrate filter (3 microns pore size) in the presence of the agonist or of the solvent alone. hrIL-5 dose-dependently stimulated normodense eosinophil chemotaxis, reaching a peak at 500 ng/ml (98 +/- 21 migrating eosinophils, n = 5, p less than 0.05). These eosinophils also responded to PAF-acether and to LTB4 and not to FMLP, hrTNF alpha, and LPS. Eosinophil preincubation with hrIL-5 increased significantly the migration by PAF-acether (173 +/- 23 migrating eosinophils with PAF-acether 10 nM after preincubation with hrIL-5 500 ng/ml vs 69 +/- 10 after preincubation with buffer alone, p less than 0.01) and failed to enhance migration by LTB4 or to uncover an activity for FMLP. Migration by PAF-acether was antagonized when the cells were preincubated with the antagonists BN 52021 and WEB 2086, which also inhibited migration by hrIL-5. Eosinophils were auto-desensitized by and to PAF-acether or LTB4, but were not cross-desensitized to each other. Eosinophils desensitized to PAF-acether failed to migrate with hrIL-5, but those desensitized to LTB4 responded to hrIL-5 as controls. hrIL-5 failed to induce the elevation of intracellular free calcium concentration and superoxide anion generation from basal values, whereas preincubation of eosinophils with hrIL-5 induced a significant increase in the rise in intracellular free calcium concentration and in superoxide anion generation by 10 nM PAF-acether but not by LTB4. In conclusion, the in vivo eosinophil migration in allergy may involve hrIL-5, particularly associated to PAF-acether.

摘要

血小板活化因子(PAF)-乙醚和白细胞介素-5(IL-5)作为哮喘中嗜酸性粒细胞增殖、活化和/或募集介质的潜在作用,促使我们研究重组人(h)IL-5(hrIL-5)和PAF-乙醚单独或联合作用于分离的豚鼠嗜酸性粒细胞的效应。从经多粘菌素B处理的豚鼠腹腔灌洗液中,通过不连续的甲泛影酰胺梯度分离出两群嗜酸性粒细胞:一群低密度的(在甲泛影酰胺的20%至22%之间,纯度:63±3%,n = 27)和另一群正常密度的(在甲泛影酰胺的22%至24%之间,纯度:87±2%,n = 16)。在微量博伊登小室上评估趋化活性,结果表示为在激动剂或仅溶剂存在下,40微米处通过硝酸纤维素滤膜(孔径3微米)迁移的嗜酸性粒细胞数量(平均值±标准误)。hrIL-5剂量依赖性地刺激正常密度嗜酸性粒细胞的趋化性,在500 ng/ml时达到峰值(98±21个迁移的嗜酸性粒细胞,n = 5,p<0.05)。这些嗜酸性粒细胞也对PAF-乙醚和白三烯B4(LTB4)有反应,而对甲酰甲硫氨酸-亮氨酸-苯丙氨酸(FMLP)、人肿瘤坏死因子α(hrTNFα)和脂多糖(LPS)无反应。用hrIL-5预孵育嗜酸性粒细胞显著增加了PAF-乙醚诱导的迁移(用500 ng/ml hrIL-5预孵育后,10 nM PAF-乙醚诱导173±23个迁移的嗜酸性粒细胞,而仅用缓冲液预孵育后为69±10个,p<0.01),但未能增强LTB4诱导的迁移,也未揭示FMLP的活性。当细胞用拮抗剂BN 52021和WEB 2086预孵育时,PAF-乙醚诱导的迁移受到拮抗,这两种拮抗剂也抑制hrIL-5诱导的迁移。嗜酸性粒细胞对PAF-乙醚或LTB4自身脱敏,但彼此之间不会交叉脱敏。对PAF-乙醚脱敏的嗜酸性粒细胞不能随hrIL-5迁移,但对LTB4脱敏的嗜酸性粒细胞对hrIL-5的反应与对照相同。hrIL-5未能诱导细胞内游离钙浓度从基础值升高以及超氧阴离子生成,而用hrIL-5预孵育嗜酸性粒细胞可导致细胞内游离钙浓度升高以及10 nM PAF-乙醚诱导的超氧阴离子生成显著增加,但LTB4诱导的则未增加。总之,过敏反应中体内嗜酸性粒细胞迁移可能涉及hrIL-5,特别是与PAF-乙醚相关。

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