Am. J. Respir. Cell Mol. Biol., Vol 14, No. 1, 01 1996, 104-112.
Mucociliary differentiation of serially passaged normal human tracheobronchial epithelial cells
TE Gray, K Guzman, CW Davis, LH Abdullah and P Nettesheim
Laboratory of Pulmonary Pathobiology, National Institutes of Environmental Health Sciences, Research Triangle Park, NC 27709, USA.
The goal of our studies was to establish procedures for subculturing normal
human tracheobronchial epithelial (NHTBE) cells without compromising their
ability to differentiate into mucous and ciliated cells (i.e.,
differentiation competence) and to study the regulation of airway
secretions by epidermal growth factor (EGF) and retinoic acid (RA). Primary
NHTBE cells were obtained from a commercial source and subcultured
repeatedly in serum-free medium on plastic tissue culture dishes. The
subcultured cells were tested after every passage for differentiation
competence in air-liquid interface (ALI) cultures. The apical secretions of
cultured NHTBE cells were characterized by immunoblotting, Western
blotting, or enzyme-linked immunosorbent assay using a variety of
antibodies. They contained mucin-like materials as well as lysozyme,
lactoferrin, and secretory leukocyte protease inhibitor (SLPI). We found
that an EGF concentration of 25 ng/ml, which is commonly used in airway
cell cultures, adversely affected growth, mucin production, and morphology
of ALI cultures and that RA was essential for mucociliary differentiation.
Without RA, the epithelium became squamous and mucin secretions decreased
300- to 900-fold. In contrast, secretion of lysozyme, lactoferrin, and SLPI
was significantly increased in RA-depleted cultures. Cells of passage 2 (P-
2) through P-4 remained competent to differentiate into mucous and ciliated
cells when grown in ALI cultures. However, mucin secretion and ciliagenesis
decreased in P-3 and P-4 cell cultures and P-3 but not P-4 cell cultures
exhibited bioelectric properties characteristic of airway epithelium. We
concluded that P-2 and P-3 NHTBE cell cultures retain many important
features of normal airway epithelium. This enables one to conduct many
studies of airway cell biology with a greatly expanded (6,000-fold) cell
pool.
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26(2):
209 - 215.
[Abstract]
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K. Million, F. Tournier, O. Houcine, P. Ancian, U. Reichert, and F. Marano
Effects of Retinoic Acid Receptor-Selective Agonists on Human Nasal Epithelial Cell Differentiation
Am. J. Respir. Cell Mol. Biol.,
December 1, 2001;
25(6):
744 - 750.
[Abstract]
[Full Text]
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K. B. Adler and Y. Li
Airway Epithelium and Mucus . Intracellular Signaling Pathways for Gene Expression and Secretion
Am. J. Respir. Cell Mol. Biol.,
October 1, 2001;
25(4):
397 - 400.
[Full Text]
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H. Danahay, L. Withey, C. T. Poll, S. F. J. van de Graaf, and R. J. Bridges
Protease-activated receptor-2-mediated inhibition of ion transport in human bronchial epithelial cells
Am J Physiol Cell Physiol,
June 1, 2001;
280(6):
C1455 - C1464.
[Abstract]
[Full Text]
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D. M. Morse, J. L. Smullen, and C. W. Davis
Differential effects of UTP, ATP, and adenosine on ciliary activity of human nasal epithelial cells
Am J Physiol Cell Physiol,
June 1, 2001;
280(6):
C1485 - C1497.
[Abstract]
[Full Text]
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