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内皮素在哮喘单核吞噬细胞炎症中的作用。

Involvement of endothelin in mononuclear phagocyte inflammation in asthma.

作者信息

Chanez P, Vignola A M, Albat B, Springall D R, Polak J M, Godard P, Bousquet J

机构信息

Clinique des Maladies Respiratoires, Hopital Arnaud de Villeneuve, Montpellier, France.

出版信息

J Allergy Clin Immunol. 1996 Aug;98(2):412-20. doi: 10.1016/s0091-6749(96)70166-5.

Abstract

BACKGROUND AND AIM

Endothelin has bronchoconstrictive, vasoactive, and inflammatory properties and may be involved in the pathogenesis of asthma. We have studied the involvement of endothelin in asthma by examining its expression and release by mononuclear phagocytes obtained from 56 patients with asthma and 32 control subjects and the activation of mononuclear phagocytes by endothelin.

METHODS

Endothelin immunoreactivity was studied by using immunocytochemistry on monocytes and alveolar macrophages. Spontaneous and lipopolysaccharide-induced endothelin release from monocytes and alveolar macrophages was studied by radioimmunoassay. The proportion of intracellular endothelin was assessed after cell disruption by Triton (Union Carbide Corp., Bound Brook, N.J.). The release of fibronectin and tumor necrosis factor-alpha induced by endothelin was studied in alveolar macrophages by enzyme immunoassay.

RESULTS

Endothelin immunoreactivity was significantly increased in cells from patients with asthma in comparison with those from the control group, but its release by alveolar macrophages was similar in both groups. Levels in the cell lysates and supernatants were similar for patients with asthma and normal subjects. Endothelin significantly increased the release of tumor necrosis factor-alpha and fibronectin by alveolar macrophages from normal subjects and patients with stable asthma, but it significantly decreased their release in patients with unstable asthma.

CONCLUSION

This study suggests a role for endothelin in airway inflammation in asthma. Endothelin may act in a different fashion on alveolar macrophages, depending on the degree of stability of the disease.

摘要

背景与目的

内皮素具有支气管收缩、血管活性和炎症特性,可能参与哮喘的发病机制。我们通过检测56例哮喘患者和32例对照者的单核吞噬细胞中内皮素的表达与释放以及内皮素对单核吞噬细胞的激活作用,研究了内皮素在哮喘中的作用。

方法

采用免疫细胞化学方法研究单核细胞和肺泡巨噬细胞中的内皮素免疫反应性。通过放射免疫分析法研究单核细胞和肺泡巨噬细胞自发及脂多糖诱导的内皮素释放。用曲拉通(联合碳化物公司,新泽西州布恩布鲁克)破坏细胞后评估细胞内内皮素的比例。通过酶免疫分析法研究内皮素诱导的肺泡巨噬细胞中纤连蛋白和肿瘤坏死因子-α的释放。

结果

与对照组相比,哮喘患者细胞中的内皮素免疫反应性显著增加,但两组肺泡巨噬细胞的内皮素释放相似。哮喘患者和正常受试者细胞裂解物和上清液中的水平相似。内皮素显著增加正常受试者和稳定期哮喘患者肺泡巨噬细胞中肿瘤坏死因子-α和纤连蛋白的释放,但在不稳定期哮喘患者中显著降低其释放。

结论

本研究提示内皮素在哮喘气道炎症中起作用。根据疾病的稳定程度,内皮素可能以不同方式作用于肺泡巨噬细胞。

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