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G 蛋白偶联腺苷受体差异限制抗原诱导的肥大细胞活化。

Gs-coupled adenosine receptors differentially limit antigen-induced mast cell activation.

机构信息

Department of Medicine, Division of Pulmonary and Critical Care Medicine, University of North Carolina at Chapel Hill, 8033 Burnett-Womack, Chapel Hill, NC 27599-7219, USA.

出版信息

J Pharmacol Exp Ther. 2013 Feb;344(2):426-35. doi: 10.1124/jpet.112.198978. Epub 2012 Nov 13.

Abstract

Mast cell activation results in the immediate release of proinflammatory mediators prestored in cytoplasmic granules, as well as initiation of lipid mediator production and cytokine synthesis by these resident tissue leukocytes. Allergen-induced mast cell activation is central to the pathogenesis of asthma and other allergic diseases. Presently, most pharmacological agents for the treatment of allergic disease target receptors for inflammatory mediators. Many of these mediators, such as histamine, are released by mast cells. Targeting pathways that limit antigen-induced mast cell activation may have greater therapeutic efficacy by inhibiting the synthesis and release of many proinflammatory mediators produced in the mast cell. In vitro studies using cultured human and mouse mast cells, and studies of mice lacking A(2B) receptors, suggest that adenosine receptors, specifically the G(s)-coupled A(2A) and A(2B) receptors, might provide such a target. Here, using a panel of mice lacking various combinations of adenosine receptors, and mast cells derived from these animals, we show that adenosine receptor agonists provide an effective means of inhibition of mast cell degranulation and induction of cytokine production both in vitro and in vivo. We identify A(2B) as the primary receptor limiting mast cell degranulation, whereas the combined activity of A(2A) and A(2B) is required for the inhibition of cytokine synthesis.

摘要

肥大细胞活化导致预先储存在细胞质颗粒中的促炎介质的即刻释放,以及这些驻留组织白细胞开始产生脂类介质和细胞因子合成。变应原诱导的肥大细胞活化是哮喘和其他过敏性疾病发病机制的核心。目前,大多数治疗过敏性疾病的药物都针对炎症介质的受体。许多此类介质(如组胺)是由肥大细胞释放的。通过靶向限制抗原诱导的肥大细胞活化的途径,通过抑制肥大细胞中产生的许多促炎介质的合成和释放,可能具有更大的治疗效果。使用培养的人肥大细胞和鼠肥大细胞进行的体外研究,以及缺乏 A(2B)受体的小鼠研究表明,腺苷受体,特别是 G(s)偶联的 A(2A)和 A(2B)受体,可能提供这样的靶点。在这里,我们使用一组缺乏各种腺苷受体组合的小鼠和源自这些动物的肥大细胞,表明腺苷受体激动剂提供了一种有效的抑制肥大细胞脱颗粒和诱导细胞因子产生的方法,无论是在体外还是体内。我们确定 A(2B)是限制肥大细胞脱颗粒的主要受体,而 A(2A)和 A(2B)的联合活性是抑制细胞因子合成所必需的。

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