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哮喘中的气道平滑肌:将收缩和机械转导与疾病发病机制及重塑相联系

Airway smooth muscle in asthma: linking contraction and mechanotransduction to disease pathogenesis and remodelling.

作者信息

Noble Peter B, Pascoe Chris D, Lan Bo, Ito Satoru, Kistemaker Loes E M, Tatler Amanda L, Pera Tonio, Brook Bindi S, Gosens Reinoud, West Adrian R

机构信息

School of Anatomy, Physiology and Human Biology, University of Western Australia, WA, Australia.

Center for Heart Lung Innovation, University of British Columbia, BC, Canada.

出版信息

Pulm Pharmacol Ther. 2014 Dec;29(2):96-107. doi: 10.1016/j.pupt.2014.07.005. Epub 2014 Jul 23.

Abstract

Asthma is an obstructive airway disease, with a heterogeneous and multifactorial pathogenesis. Although generally considered to be a disease principally driven by chronic inflammation, it is becoming increasingly recognised that the immune component of the pathology poorly correlates with the clinical symptoms of asthma, thus highlighting a potentially central role for non-immune cells. In this context airway smooth muscle (ASM) may be a key player, as it comprises a significant proportion of the airway wall and is the ultimate effector of acute airway narrowing. Historically, the contribution of ASM to asthma pathogenesis has been contentious, yet emerging evidence suggests that ASM contractile activation imparts chronic effects that extend well beyond the temporary effects of bronchoconstriction. In this review article we describe the effects that ASM contraction, in combination with cellular mechanotransduction and novel contraction-inflammation synergies, contribute to asthma pathogenesis. Specific emphasis will be placed on the effects that ASM contraction exerts on the mechanical properties of the airway wall, as well as novel mechanisms by which ASM contraction may contribute to more established features of asthma such as airway wall remodelling.

摘要

哮喘是一种阻塞性气道疾病,其发病机制具有异质性和多因素性。尽管通常认为哮喘主要由慢性炎症驱动,但人们越来越认识到,病理过程中的免疫成分与哮喘的临床症状相关性较差,这凸显了非免疫细胞可能发挥的核心作用。在这种情况下,气道平滑肌(ASM)可能是关键因素,因为它在气道壁中占很大比例,并且是急性气道狭窄的最终效应器。从历史上看,ASM对哮喘发病机制的贡献一直存在争议,但新出现的证据表明,ASM收缩激活产生的慢性影响远远超出了支气管收缩的暂时效应。在这篇综述文章中,我们描述了ASM收缩与细胞机械转导以及新的收缩-炎症协同作用相结合,对哮喘发病机制的影响。将特别强调ASM收缩对气道壁力学特性的影响,以及ASM收缩可能导致哮喘更典型特征(如气道壁重塑)的新机制。

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