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腺苷、肥大细胞与哮喘。

Adenosine, mast cells and asthma.

作者信息

Forsythe P, Ennis M

机构信息

Department of Clinical Biochemistry, The Queen's University of Belfast, UK.

出版信息

Inflamm Res. 1999 Jun;48(6):301-7. doi: 10.1007/s000110050464.

Abstract

The aim of this article is to review the interplay between adenosine and mast cells in asthma. Adenosine is an endogenous nucleoside released from metabolically active cells and generated extracellularly via the degradation of released ATP. It is a potent biological mediator that modulates the activity of numerous cell types including platelets, neutrophils and mast cells via action at specific adenosine receptors (A1, A2a, A2b, A3). These receptors are expressed on mast cells but the exact pattern of receptor subtype expression depends on the source of the mast cells. Adenosine is also a potent bronchoconstricting agent and is suggested to contribute to the pathophysiology of asthma. Evidence is provided to suggest that the nucleoside exerts its influence on the asthmatic condition through its ability to modulate the release of mast cell derived mediators. However, the mechanism of adenosine/mast cell interaction which contributes to asthma remains unclear. Progress in the area has been hampered by the heterogeneity of mast cell responses and a lack of highly specific receptor agonists and antagonists. The expression of different adenosine receptor subtypes on mast cells is described. The final section of the review presents data to suggest that BAL mast cells may provide an accurate and relevant model for future investigations and together with the development of superior pharmacological tools, may aid the realisation of the therapeutic potential of adenosine/mast cell interactions in asthma. In conclusion, the role of adenosine in asthma is clearly complex. A better understanding of the contribution of adenosine to the asthmatic condition may lead to novel therapeutic approaches in the treatment of the disease.

摘要

本文旨在综述哮喘中腺苷与肥大细胞之间的相互作用。腺苷是一种内源性核苷,由代谢活跃的细胞释放,并通过释放的ATP在细胞外降解产生。它是一种强效生物介质,通过作用于特定的腺苷受体(A1、A2a、A2b、A3)来调节多种细胞类型的活性,包括血小板、中性粒细胞和肥大细胞。这些受体在肥大细胞上表达,但受体亚型表达的确切模式取决于肥大细胞的来源。腺苷也是一种强效支气管收缩剂,被认为与哮喘的病理生理学有关。有证据表明,这种核苷通过调节肥大细胞衍生介质的释放对哮喘病情产生影响。然而,腺苷/肥大细胞相互作用导致哮喘的机制仍不清楚。该领域的进展受到肥大细胞反应异质性以及缺乏高度特异性受体激动剂和拮抗剂的阻碍。本文描述了肥大细胞上不同腺苷受体亚型的表达。综述的最后一部分提供的数据表明,支气管肺泡灌洗肥大细胞可能为未来的研究提供一个准确且相关的模型,并且随着更先进药理学工具的开发,可能有助于实现腺苷/肥大细胞相互作用在哮喘治疗中的潜在治疗价值。总之,腺苷在哮喘中的作用显然很复杂。更好地理解腺苷对哮喘病情的影响可能会带来治疗该疾病的新方法。

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