In vitro and ex vivo models of human asthma

被引:74
作者
Blume, Cornelia
Davies, Donna E.
机构
[1] Univ Southampton, Southampton Univ Hosp, Brooke Lab, Southampton SO16 6YD, Hants, England
[2] Univ Southampton, Southampton Univ Hosp, Southampton NIHR, Resp Biomed Res Unit, Southampton SO16 6YD, Hants, England
基金
英国医学研究理事会;
关键词
Asthma; In vitro models; Bronchial epithelium; Inflammation; Remodelling; BRONCHIAL EPITHELIAL-CELLS; CUT LUNG SLICES; RESPIRATORY SYNCYTIAL VIRUS; DIESEL EXHAUST PARTICLES; AIRWAY WALL MODEL; BARRIER FUNCTION; ANIMAL-MODELS; 3-DIMENSIONAL CULTURE; NONASTHMATIC SUBJECTS; CYTOKINE PRODUCTION;
D O I
10.1016/j.ejpb.2012.12.014
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
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. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:394 / 400
页数:7
相关论文
共 111 条
[1]
Untangling asthma phenotypes and endotypes [J].
Agache, I. ;
Akdis, C. ;
Jutel, M. ;
Virchow, J. C. .
ALLERGY, 2012, 67 (07) :835-846
[2]
Genome-wide association studies for discovery of genes involved in asthma [J].
Akhabir, Loubna ;
Sandford, Andrew J. .
RESPIROLOGY, 2011, 16 (03) :396-406
[3]
[Anonymous], 2003, European Lung White Book
[4]
[Anonymous], 2011, From the Global Strategy for Asthma Management and Prevention
[5]
[Anonymous], EUR J PHARM BIOPHARM
[6]
Functional Effects of Nanoparticle Exposure on Calu-3 Airway Epithelial Cells [J].
Banga, Amiraj ;
Witzmann, Frank A. ;
Petrache, Horia I. ;
Blazer-Yost, Bonnie L. .
CELLULAR PHYSIOLOGY AND BIOCHEMISTRY, 2012, 29 (1-2) :197-212
[7]
Comparison of ciliary activity and inflammatory mediator release from bronchial epithelial cells of nonatopic nonasthmatic subjects and atopic asthmatic patients and the effect of diesel exhaust particles in vitro [J].
Bayram, H ;
Devalia, JL ;
Khair, OA ;
Abdelaziz, MM ;
Sapsford, RJ ;
Sagai, M ;
Davies, RJ .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1998, 102 (05) :771-782
[8]
Effect of ozone and nitrogen dioxide on the permeability of bronchial epithelial cell cultures of non-asthmatic and asthmatic subjects [J].
Bayram, H ;
Rusznak, C ;
Khair, OA ;
Sapsford, RJ ;
Abdelaziz, MM .
CLINICAL AND EXPERIMENTAL ALLERGY, 2002, 32 (09) :1285-1292
[9]
Human asthma phenotypes: from the clinic, to cytokines, and back again [J].
Bhakta, Nirav R. ;
Woodruff, Prescott G. .
IMMUNOLOGICAL REVIEWS, 2011, 242 :220-232
[10]
Macrophages and dendritic cells express tight junction proteins and exchange particles in an in vitro model of the human airway wall [J].
Blank, Fabian ;
Wehrli, Marc ;
Lehmann, Andrea ;
Baum, Oliver ;
Gehr, Peter ;
von Garnier, Christophe ;
Rothen-Rutishauser, Barbara M. .
IMMUNOBIOLOGY, 2011, 216 (1-2) :86-95