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血小板在过敏性炎症中对白细胞募集至关重要。

Platelets are essential for leukocyte recruitment in allergic inflammation.

作者信息

Pitchford Simon C, Yano Hiroshi, Lever Rebecca, Riffo-Vasquez Yanira, Ciferri Silvia, Rose Mark J, Giannini Silvia, Momi Stefania, Spina Domenico, O'connor Brian, Gresele Paolo, Page Clive P

机构信息

Sackler Institute of Pulmonary Pharmacology, GKT School of Biomedical Sciences, King's College London, London.

出版信息

J Allergy Clin Immunol. 2003 Jul;112(1):109-18. doi: 10.1067/mai.2003.1514.

Abstract

BACKGROUND

The role of platelets in inflammation is recognized but poorly characterized, and little is known of their interaction with leukocytes. However, platelet-leukocyte interactions have been demonstrated in cardiovascular disease, culminating in enhanced leukocyte recruitment.

OBJECTIVES

This study was undertaken to assess the possibility and potential role of similar phenomena occurring in asthmatic patients, a murine model of allergic inflammation, and in vitro adhesion studies.

METHODS

Asthmatic patients had blood taken at various time points to document the degree of leukocyte activation and the presence of platelet-leukocyte aggregates through FACS analysis before and after allergen exposure. Similar studies were carried out in mice exposed to allergen after previous sensitization, with some groups being selectively depleted of platelets through both an immunologic (antiplatelet antiserum) and nonimmunologic (busulfan) method. Additionally, lavage fluid and airway tissue were analyzed to assess the degree of pulmonary leukocyte recruitment. The importance of platelets on leukocyte adhesion to the endothelium was then assessed with in vitro incubation of radiolabeled leukocytes in the presence of activated platelets on cultured human vascular endothelial cells.

RESULTS

We have observed circulating platelet-leukocyte aggregates in the blood of allergic asthmatic patients during the allergen-induced late asthmatic response and in sensitized mice after allergen exposure. In platelet-depleted mice infiltration of leukocytes into airways after allergen challenge was significantly reduced and could be restored by means of infusion of platelets from allergic animals, indicating an essential role for platelets in leukocyte recruitment. CD11b expression on leukocytes involved in aggregates with platelets, although not on free leukocytes, was upregulated. Furthermore, the presence of autologous platelets augmented the adhesion of human polymorphonuclear leukocytes to cultured vascular endothelial cells, an effect that was found to be endothelial cell dependent and to involve platelet activation.

CONCLUSION

These results suggest that platelet participation in cell recruitment occurs at the level of the circulation and might involve the priming of leukocytes for subsequent adhesion and transmigration into tissues.

摘要

背景

血小板在炎症中的作用已得到认可,但特征尚不明确,其与白细胞的相互作用也知之甚少。然而,血小板与白细胞的相互作用已在心血管疾病中得到证实,最终导致白细胞募集增加。

目的

本研究旨在评估在哮喘患者、过敏性炎症小鼠模型以及体外黏附研究中出现类似现象的可能性及潜在作用。

方法

在不同时间点采集哮喘患者的血液,通过流式细胞术分析过敏原暴露前后白细胞活化程度及血小板 - 白细胞聚集体的存在情况。对先前致敏后暴露于过敏原的小鼠进行类似研究,部分组通过免疫(抗血小板抗血清)和非免疫(白消安)方法选择性清除血小板。此外,分析灌洗液和气道组织以评估肺白细胞募集程度。然后在培养的人血管内皮细胞上,在活化血小板存在的情况下,通过体外孵育放射性标记的白细胞,评估血小板对白细胞黏附于内皮的重要性。

结果

我们观察到,在过敏性哮喘患者血液中,过敏原诱导的迟发性哮喘反应期间以及致敏小鼠过敏原暴露后,存在循环血小板 - 白细胞聚集体。在血小板耗竭的小鼠中,过敏原激发后白细胞向气道的浸润显著减少,通过输注来自过敏动物的血小板可使其恢复,这表明血小板在白细胞募集中起重要作用。与血小板形成聚集体的白细胞上 CD11b 的表达上调,而游离白细胞上未上调。此外,自体血小板的存在增强了人多形核白细胞对培养的血管内皮细胞的黏附,这一效应被发现依赖于内皮细胞且涉及血小板活化。

结论

这些结果表明,血小板参与细胞募集发生在循环水平,可能涉及白细胞的预激活,以便随后黏附和迁移到组织中。

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