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人哮喘的体外和离体模型。

In vitro and ex vivo models of human asthma.

机构信息

Brooke Laboratory, Clinical and Experimental Sciences and the Southampton NIHR, Respiratory Biomedical Research Unit, University of Southampton, University Hospital Southampton, Southampton, United Kingdom.

出版信息

Eur J Pharm Biopharm. 2013 Jun;84(2):394-400. doi: 10.1016/j.ejpb.2012.12.014. Epub 2013 Jan 9.

Abstract

Asthma is an inflammatory disorder of the conducting airways which undergo distinct structural and functional changes leading to non-specific bronchial hyperresponsiveness (BHR) and airflow obstruction that fluctuate over time. It is a complex disease involving multiple genetic and environmental influences whose multifactorial interactions can result in a range of asthma phenotypes. Since our understanding of these gene-gene and gene-environment interactions is very poor, this poses a major challenge to the logical development of 'models of asthma'. However, use of cells and tissues from asthmatic donors allows genetic and epigenetic influences to be evaluated and can go some way to reflect the complex interplay between genetic and environmental stimuli that occur in vivo. Current alternative approaches to in vivo animal models involve use of a plethora of systems ranging from very simple models using human cells (e.g. bronchial epithelial cells and fibroblasts) in mono- or co-culture, whole tissue explants (biopsies, muscle strips, bronchial rings) through to in vivo studies in human volunteers. Asthma research has been greatly facilitated by the introduction of fibreoptic bronchoscopy which is now a commonly used technique in the field of respiratory disease research, allowing collection of biopsy specimens, bronchial brushing samples, and bronchoalveolar lavage fluid enabling use of disease-derived cells and tissues in some of these models. Here, we will consider the merits and limitations of current models and discuss the potential of tissue engineering approaches through which we aim to advance our understanding of asthma and its treatment.

摘要

哮喘是一种气道炎症性疾病,会发生明显的结构和功能变化,导致非特异性支气管高反应性(BHR)和气流阻塞,这些变化随时间波动。它是一种复杂的疾病,涉及多种遗传和环境影响,其多因素相互作用可导致一系列哮喘表型。由于我们对这些基因-基因和基因-环境相互作用的了解非常有限,这对“哮喘模型”的逻辑发展构成了重大挑战。然而,使用哮喘供体的细胞和组织可以评估遗传和表观遗传影响,并在一定程度上反映体内遗传和环境刺激之间的复杂相互作用。目前替代体内动物模型的方法涉及使用大量系统,从使用人类细胞(例如支气管上皮细胞和成纤维细胞)进行单一或共培养的非常简单的模型,到整个组织外植体(活检、肌肉条、支气管环),再到人类志愿者的体内研究。纤维光学支气管镜的引入极大地促进了哮喘研究,它现在是呼吸疾病研究领域常用的技术,允许收集活检标本、支气管刷检样本和支气管肺泡灌洗液,从而在这些模型中的一些中使用疾病来源的细胞和组织。在这里,我们将考虑当前模型的优点和局限性,并讨论组织工程方法的潜力,我们旨在通过该方法来提高对哮喘及其治疗的认识。

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