## Abstract In cellβfree translations of RNA from primary cultures of pig trachea surface epithelial cells we observed that a mRNA encoding a 20kDa prolineβrich protein (sPRP) was dramatically induced during culturing (Tesfaigzi et al., 1990, Biochem. Biophys. Res. Commun., __172:M__1304β1309). Thi
Differential expression of a WD protein during squamous differentiation of tracheal epithelial cells
β Scribed by Y.S. Kim; S.M. Hwang; S.J. Lee; J.S. Jung
- Publisher
- John Wiley and Sons
- Year
- 2002
- Tongue
- English
- Weight
- 198 KB
- Volume
- 86
- Category
- Article
- ISSN
- 0730-2312
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β¦ Synopsis
The lining of the trachea consists of a pseudostratified, mucociliary epithelium that under a variety of conditions, such as vitamin A deficiency, toxic and mechanical injury, becomes a stratified squamous epithelium. Several in vitro cell culture models have been established to study the process of differentiation of airway epithelium. Such studies have indicated that mucosecretory differentiation of tracheal epithelial cells can be modulated by substratum. This study was undertaken to understand molecular mechanisms of squamous differentiation in tracheal epithelia. Primary cultured tracheal cells grown on uncoated filters were differentiated to single layer of squamous cells, whereas cells were grown as stratified columnar cells on collagen-I coated filters. The responses to secretagogues were altered according to culture conditions. DD-PCR revealed that FAK and a WD protein expression was increased in squamous tracheal epithelia. Expression of a WD protein was changed by the treatment of retinoic acid in various epithelial cells. These results indicated that squamous differentiation of tracheal cells changes the expression of a variety of genes, and that the experimental model for this study can be employed to study molecular mechanisms of squamous differentiation in airway epithelial cells.
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