Primary bronchial epithelial cell culture from explanted cystic fibrosis lungs

被引:15
作者
Brodlie, Malcolm [1 ]
McKean, Michael C. [2 ]
Johnson, Gail E. [1 ]
Perry, John D. [3 ]
Nicholson, Audrey [3 ]
Verdon, Bernard [4 ]
Gray, Michael A. [4 ]
Dark, John H. [1 ]
Pearson, Jeffrey P. [4 ]
Fisher, Andrew J. [1 ]
Corris, Paul A. [1 ]
Lordan, James [1 ]
Ward, Christopher [1 ]
机构
[1] Newcastle Univ, Inst Cellular Med, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
[2] Newcastle Upon Tyne Hosp NHS Fdn Trust, Paediat Resp Unit, Newcastle Upon Tyne, Tyne & Wear, England
[3] Newcastle Upon Tyne Hosp NHS Fdn Trust, Freeman Hosp, Dept Microbiol, Newcastle Upon Tyne, Tyne & Wear, England
[4] Newcastle Univ, Inst Cell & Mol Biosci, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
关键词
cystic fibrosis; lung transplantation; primary bronchial epithelial cells; CHLORIDE CONDUCTANCE; CFTR GENE; ION; TRANSFORMATION; DISRUPTION; AIRWAYS; MODEL;
D O I
10.3109/01902140903165265
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Lung disease is responsible for more than 95% of morbidity and mortality in cystic fibrosis. The exact pathogenesis of cystic fibrosis lung disease remains poorly understood. Experimental models are therefore vital for use in research. Animal models and immortalized cell lines both have inherent limitations. Explanted lungs removed from people with cystic fibrosis at the time of transplantation represent a potentially valuable but technically and logistically challenging source of primary cystic fibrosis bronchial epithelial cells. In this study, pieces of segmental bronchus from explanted lungs were treated with patient-specific antimicrobials prior to isolation of bronchial epithelial cells. Cultured cells were characterized by their morphology under light microscopy, cytokeratin and hematoxylin-eosin staining, and electrophysiological profile. Primary bronchial epithelial cells were successfully cultured from 15 of 22 patients attempted. The cells exhibited typical epithelial morphology, staining for cytokeratin, lack of responsiveness to forskolin treatment, and remained viable after storage in liquid nitrogen. Seven unsuccessful cultures failed due to early infection with bacteria known to colonize the airways pretransplant. The results show that primary bronchial epithelial cell culture is possible from explanted cystic fibrosis lungs. This provides an important cellular model to elucidate the pathogenic mechanisms in cystic fibrosis lung disease and to investigate potential therapeutic targets.
引用
收藏
页码:101 / 110
页数:10
相关论文
共 43 条
[1]   Incidence of primary neoplasms in explanted lungs: Long-term follow-up from 214 lung transplant patients [J].
Abrahams, NA ;
Meziane, M ;
Ramalingam, P ;
Mehta, A ;
DeCamp, M ;
Farver, CF .
TRANSPLANTATION PROCEEDINGS, 2004, 36 (09) :2808-2811
[2]   Update in cystic fibrosis 2007 [J].
Accurso, Frank J. .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2008, 177 (10) :1058-1061
[3]   Squamous metaplasia amplifies pathologic epithelial-mesenchymal interactions in COPD patients [J].
Araya, Jun ;
Cambier, Stephanie ;
Markovics, Jennifer A. ;
Wolters, Paul ;
Jablons, David ;
Hill, Arthur ;
Finkbeiner, Walter ;
Jones, Kirk ;
Broaddus, V. Courtney ;
Sheppard, Dean ;
Barzcak, Andrea ;
Xiao, Yuanyuan ;
Erle, David J. ;
Nishimura, Stephen L. .
JOURNAL OF CLINICAL INVESTIGATION, 2007, 117 (11) :3551-3562
[4]   The signals and pathways activating cellular senescence [J].
Ben-Porath, I ;
Weinberg, RA .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2005, 37 (05) :961-976
[5]   Ion and fluid transport properties of small airways in cystic fibrosis [J].
Blouquit, Sabine ;
Regnier, Agathe ;
Dannhoffer, Luc ;
Fermanian, Christophe ;
Naline, Emmanuel ;
Boucher, Richard ;
Chinet, Thierry .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2006, 174 (03) :299-305
[6]   Front-runners for pharmacotherapeutic correction of the airway ion transport defect in cystic fibrosis [J].
Clunes, Mark T. ;
Boucher, Richard C. .
CURRENT OPINION IN PHARMACOLOGY, 2008, 8 (03) :292-299
[7]  
Davidson D J, 2001, Trends Genet, V17, pS29, DOI 10.1016/S0168-9525(01)02452-0
[8]   LUNG-DISEASE IN THE CYSTIC-FIBROSIS MOUSE EXPOSED TO BACTERIAL PATHOGENS [J].
DAVIDSON, DJ ;
DORIN, JR ;
MCLACHLAN, G ;
RANALDI, V ;
LAMB, D ;
DOHERTY, C ;
GOVAN, J ;
PORTEOUS, DJ .
NATURE GENETICS, 1995, 9 (04) :351-357
[9]   Cystic fibrosis mortality and survival in the UK: 1947-2003 [J].
Dodge, J. A. ;
Lewis, P. A. ;
Stanton, M. ;
Wilsher, J. .
EUROPEAN RESPIRATORY JOURNAL, 2007, 29 (03) :522-526
[10]   Clinical trials in cystic fibrosis [J].
Doering, Gerd ;
Elborn, J. Stuart ;
Johannesson, Marie ;
de Jonge, Hugo ;
Griese, Matthias ;
Smyth, Alan ;
Heijerman, Harry .
JOURNAL OF CYSTIC FIBROSIS, 2007, 6 (02) :85-99