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嗜酸性粒细胞VLA-4与纤连蛋白结合通过5-脂氧合酶激活加剧支气管狭窄。

Eosinophil VLA-4 binding to fibronectin augments bronchial narrowing through 5-lipoxygenase activation.

作者信息

Muñoz N M, Rabe K F, Neeley S P, Herrnreiter A, Zhu X, McAllister K, Mayer D, Magnussen H, Galens S, Leff A R

机构信息

Department of Medicine, University of Chicago, IL 60637, USA.

出版信息

Am J Physiol. 1996 Apr;270(4 Pt 1):L587-94. doi: 10.1152/ajplung.1996.270.4.L587.

Abstract

We examined the effect of ligation of human eosinophils activated by platelet-activating factor (PAF) to soluble human fibronectin (FN) on the augmented contractile response of human bronchial explants. Styrene microplate wells were FN-coated and eosinophils were allowed to adhere in the presence of 1) buffer control, 2) 20 micrograms/ml monoclonal antibody (HP2/1) to the alpha 4 beta 1 ligand (VLA-4) on the eosinophils, 3) 20 micrograms/ml anti-CD18 R15.7, 4) 20 micrograms/ml anti-CD16 3G8, or 5) 10(-6) M A63162, a 5-lipoxygenase inhibitor. Sixty minutes later, treated cells were activated with either buffer or 10(-6) M PAF. Airway luminal diameter was assessed by computerized videomicrometry as a function of pixel number, and activation of eosinophils was confirmed by measurement of leukotriene C4 (LTC4) secretion. Ligation with FN caused an increase in PAF-stimulated LTC4 secretion from 276 +/- 75.6 pg/10(6) cell at baseline to 606 +/- 90.2 pg/10(6) cell (P < 0.01). This corresponded to augmented luminal narrowing of human bronchial explants from 25.3 +/- 9.39% (PAF activation alone) to 42.9 +/- 8.0% (PAF-activated eosinophils + FN) (P < 0.01). Both augmented airway luminal narrowing and increased LTC4 secretion caused by PAF-activated cells after FN ligation were blocked completely by anti-VLA-4 MAb (P < 0.05 vs. control). Pretreatment with 10(-6) MA63162 inhibited completely the PAF-stimulated LTC4 secretion to baseline level ( P < 0.001). Inhibition of 5-lipoxygenase similarly blocked luminal narrowing caused by eosinophils stimulated by PAF by > 95% (P < 0.001). We demonstrate that the binding of human eosinophils to the matrix protein FN causes augmented secretion of LTC4 which, in turn, causes augmented luminal narrowing of explanted human bronchi in vitro. We also demonstrate that the augmented activity is blocked selectively by pretreatment with specific monoclonal antibody against VLA-4 and blockade of eosinophil 5-lipoxygenase inhibits both LTC4 secretion and airway narrowing after PAF-stimulation.

摘要

我们研究了血小板活化因子(PAF)激活的人嗜酸性粒细胞与可溶性人纤连蛋白(FN)结合对人支气管外植体收缩反应增强的影响。用FN包被苯乙烯微孔板孔,使嗜酸性粒细胞在以下条件下黏附:1)缓冲液对照;2)20微克/毫升抗嗜酸性粒细胞α4β1配体(VLA - 4)的单克隆抗体(HP2/1);3)20微克/毫升抗CD18 R15.7;4)20微克/毫升抗CD16 3G8;或5)10^(-6) M A63162,一种5 - 脂氧合酶抑制剂。60分钟后,用缓冲液或10^(-6) M PAF激活处理过的细胞。通过计算机化视频显微镜测量气道腔直径作为像素数的函数,并通过测量白三烯C4(LTC4)分泌来确认嗜酸性粒细胞的激活。与FN结合使PAF刺激的LTC4分泌从基线时的276±75.6皮克/10^6细胞增加到606±90.2皮克/10^6细胞(P < 0.01)。这对应于人支气管外植体管腔狭窄从单独PAF激活时的25.3±9.39%增加到PAF激活的嗜酸性粒细胞 + FN时的42.9±8.0%(P < 0.01)。FN结合后PAF激活的细胞引起的气道管腔狭窄增加和LTC4分泌增加均被抗VLA - 4单克隆抗体完全阻断(与对照相比,P < 0.05)。用10^(-6) M A63162预处理可将PAF刺激的LTC4分泌完全抑制至基线水平(P < 0.001)。抑制5 - 脂氧合酶同样可将PAF刺激的嗜酸性粒细胞引起的管腔狭窄阻断> 95%(P < 0.001)。我们证明人嗜酸性粒细胞与基质蛋白FN的结合导致LTC4分泌增加,进而导致体外人支气管外植体管腔狭窄增加。我们还证明,用针对VLA - 4的特异性单克隆抗体预处理可选择性地阻断增强的活性,并且阻断嗜酸性粒细胞5 - 脂氧合酶可抑制PAF刺激后的LTC4分泌和气道狭窄。

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