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绵羊中性粒细胞在体内外对炎症介质的迁移反应。

Migratory responses of ovine neutrophils to inflammatory mediators in vitro and in vivo.

作者信息

Mulder K, Colditz I G

机构信息

CSIRO Division of Animal Health, Armidale, Australia.

出版信息

J Leukoc Biol. 1993 Mar;53(3):273-8. doi: 10.1002/jlb.53.3.273.

DOI:10.1002/jlb.53.3.273
PMID:8384237
Abstract

The migration of 111In-labeled ovine neutrophils towards a range of inflammatory mediators was examined in vitro using a 48-well chemotaxis chamber. Typical curves were obtained for the chemotactic response to zymosan-activated plasma (ZAP, a source of C5a) and interleukin-8 (IL-8). In contrast, leukotriene B4 (LTB4), platelet-activating factor (PAF), interleukin-1 alpha (IL-1 alpha), tumor necrosis factor alpha (TNF-alpha), N-formyl-methionine-leucyl-phenylalanine (fMLP), and endotoxins from Escherichia coli and Pseudomonas aeruginosa failed to induce neutrophil migration in vitro. Of these mediators LTB4, ZAP, IL-1 alpha, TNF-alpha, IFN-gamma, and IL-8 have been reported to induce neutrophil accumulation in skin of sheep, and in the current study E. coli endotoxin was a potent inducer of 111In-labeled neutrophil accumulation and plasma leakage in skin. In contrast, PAF induced intense plasma leakage but failed to induce accumulation of 111In-labeled neutrophils in skin. Histologic examination of skin sites receiving PAF confirmed the failure of PAF to stimulate neutrophil extravasation. FMLP lacked inflammatory activity in skin. Coinjection of actinomycin D did not abrogate recruitment of neutrophils to skin sites receiving LTB4; thus neither induction of endothelial adhesion molecules nor synthesis of IL-8 was necessary for LTB4 to exhibit inflammatory activity in vivo.

摘要

使用48孔趋化性小室在体外检测了111铟标记的绵羊中性粒细胞向一系列炎症介质的迁移情况。获得了对酵母聚糖激活血浆(ZAP,一种C5a来源)和白细胞介素-8(IL-8)趋化反应的典型曲线。相比之下,白三烯B4(LTB4)、血小板活化因子(PAF)、白细胞介素-1α(IL-1α)、肿瘤坏死因子α(TNF-α)、N-甲酰甲硫氨酰亮氨酰苯丙氨酸(fMLP)以及大肠杆菌和铜绿假单胞菌的内毒素在体外未能诱导中性粒细胞迁移。在这些介质中,LTB4、ZAP、IL-1α、TNF-α、干扰素-γ(IFN-γ)和IL-8已被报道可诱导绵羊皮肤中的中性粒细胞聚集,并且在当前研究中,大肠杆菌内毒素是111铟标记的中性粒细胞在皮肤中聚集和血浆渗漏的有效诱导剂。相比之下,PAF可诱导强烈的血浆渗漏,但未能诱导111铟标记的中性粒细胞在皮肤中聚集。对接受PAF的皮肤部位进行组织学检查证实PAF未能刺激中性粒细胞渗出。FMLP在皮肤中缺乏炎症活性。联合注射放线菌素D并未消除中性粒细胞向接受LTB4的皮肤部位的募集;因此,对于LTB4在体内表现出炎症活性而言,诱导内皮黏附分子或合成IL-8均非必要条件。

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