Tight junction properties of the immortalized human bronchial epithelial cell lines Calu-3 and 16HBE14o-

Citation
H. Wan et al., Tight junction properties of the immortalized human bronchial epithelial cell lines Calu-3 and 16HBE14o-, EUR RESP J, 15(6), 2000, pp. 1058-1068
Citations number
42
Categorie Soggetti
Cardiovascular & Respiratory Systems","da verificare
Journal title
EUROPEAN RESPIRATORY JOURNAL
ISSN journal
09031936 → ACNP
Volume
15
Issue
6
Year of publication
2000
Pages
1058 - 1068
Database
ISI
SICI code
0903-1936(200006)15:6<1058:TJPOTI>2.0.ZU;2-Y
Abstract
Tight junctions (TJs) make a vital contribution to the barrier properties o f the airway lining. Opening of TJs, or their frank cleavage, is suspected as a pathophysiological event in the lung, but research into the cellular a nd molecular mechanisms involved has been impeded by technical limitations of available experimental models. The authors have compared the properties of two epithelial cell lines derived from bronchial epithelium to explore w hether these cell lines could constitute appropriate tools for the study of TJ regulation in bronchial epithelium. Investigations of TJs in 16HBE14o- cells and Calu-3 cells were made by fluo rescent antibody labelling in conjunction with wide-field, confocal or 2-ph oton molecular excitation microscopy (2PMEM). The presence of TJ proteins w as confirmed by immunoblotting and functional properties of the monolayers were studied by measurements of transepithelial electrical resistance and m annitol permeability. Cells of both lines formed confluent monolayers In which the cells expresse d the TJ proteins occludin and ZO-1 in continuous circumferential patterns suggestive of func tional TJs. This interpretation was supported by the dev elopment of transepithelial electrical resistances and of low paracellular permeability to solutes. Within the limits of resolution offered by 2PMEM, occludin and ZO-1 appeared to colocalize at TJs. These studies suggest that the 16HBE14o- cells and Calu3 cell lines are pot entially useful in vitro models to study how tight junction opening or clea vage changes the functional barrier properties of bronchial epithelium.