Cultured human nasal epithelial multicellular spheroids: polar cyst-like model tissues.

We report here a new readily cultured nonadherent hollow spheroidal epithelial tissue model: human nasal epithelial multicellular spheroids, prepared from brushings of human nasal epithelium in vivo. Although cultured cyst-like epithelial models developed from embryonic, transformed, or polypoid tissues have been reported previously, human nasal epithelial multicellular spheroids are derived from normal mature nontransformed human airway epithelial cells. In our studies, spheroids ranged in size from 50 to 700 microns diameter (averaging approximately 250 microns). Cells of the spheroid displayed morphological polarity and formed junctional complexes. Transcellular electrolyte transport may underlie the increase in spheroid size which occurred in culture. The ease and simplicity of the brushing and culture procedures reported here render normal and diseased human cell populations more readily accessible to investigation. We believe human nasal epithelial multicellular spheroids may have important applications in the study of electrolyte and fluid transport processes, ciliary motility, epithelial polarity, cellular metabolism, and drug cytotoxicity in normal and pathophysiological states of the human respiratory tract (e.g., cystic fibrosis).

[1]  M. Knowles,et al.  Evidence for reduced Cl‐ and increased Na+ permeability in cystic fibrosis human primary cell cultures. , 1988, The Journal of physiology.

[2]  A. Evan,et al.  Polarized epithelial cysts in vitro: a review of cell and explant culture systems that exhibit epithelial cyst formation. , 1988, Scanning microscopy.

[3]  U. Pipkorn,et al.  A brush method to harvest cells from the nasal mucosa for microscopic and biochemical analysis. , 1988, Journal of immunological methods.

[4]  M. Welsh Electrolyte transport by airway epithelia. , 1987, Physiological reviews.

[5]  M. Knowles,et al.  Pharmacotherapy of airway disease in cystic fibrosis , 1987 .

[6]  R. Frizzell Cystic Fibrosis: a disease of ion channels? , 1987, Trends in Neurosciences.

[7]  A. Evan,et al.  Morphogenetic clonal growth of kidney epithelial cell line MDCK , 1987, The Anatomical record.

[8]  C. Harris Human tissues and cells in carcinogenesis research. , 1987, Cancer research.

[9]  M. Knowles,et al.  Culture of human nasal epithelial cells on collagen matrix supports. A comparison of bioelectric properties of normal and cystic fibrosis epithelia. , 1985, The American review of respiratory disease.

[10]  M. Knowles,et al.  Growth and differentiation of human nasal epithelial cells in culture. Serum-free, hormone-supplemented medium and proteoglycan synthesis. , 1985, The American review of respiratory disease.

[11]  J. Willey,et al.  Effects of formaldehyde, acetaldehyde, benzoyl peroxide, and hydrogen peroxide on cultured normal human bronchial epithelial cells. , 1985, Cancer research.

[12]  J. Widdicombe,et al.  Electrical properties of monolayers cultured from cells of human tracheal mucosa. , 1985, Journal of applied physiology.

[13]  P. Cole,et al.  Nasal brushing for the study of ciliary ultrastructure. , 1982, Journal of clinical pathology.

[14]  J. Rutland,et al.  NON-INVASIVE SAMPLING OF NASAL CILIA FOR MEASUREMENT OF BEAT FREQUENCY AND STUDY OF ULTRASTRUCTURE , 1980, The Lancet.