IN-VITRO INVESTIGATION ON PROLIFERATIVE CYSTIC KERATINIZING SQUAMOUS LESIONS IN THE RAT LUNG

Authors
Citation
M. Emura et C. Dacosta, IN-VITRO INVESTIGATION ON PROLIFERATIVE CYSTIC KERATINIZING SQUAMOUS LESIONS IN THE RAT LUNG, Experimental and toxicologic pathology, 45(4), 1993, pp. 189-195
Citations number
16
Categorie Soggetti
Pathology,Toxicology
ISSN journal
09402993
Volume
45
Issue
4
Year of publication
1993
Pages
189 - 195
Database
ISI
SICI code
0940-2993(1993)45:4<189:IIOPCK>2.0.ZU;2-F
Abstract
The proliferative cystic squamous cell lesion inducible by inhalation of particulate matter in the rat lung is characterized by the formatio n of keratin-filled cystic cavities of various sizes bordered by multi ple layers of keratinizing squamous epithelial cells. The current inve stigation is primarily concerned with two points. One is whether the c ells participating in this particular cystic configuration can recapit ulate their specific in vivo morphogenetic behavior also in the in vit ro circumstances. The other is whether these squamous epithelial cells are neoplastic in nature. Although the currently adopted cell culture system was two-dimensional, the specific morphogenetic pattern was re produced in vitro in a corresponding manner by the squamous cells deri ved from the aforementioned rat lung lesions. Exposure of these cells to 12-O-tetradecanoyl-phorbol-13-acetate (TPA) at 100 ng/ml induced a marked polymorphism in them and also stimulated their keratinization. In soft agar culture, both TPA-exposed and unexposed cells developed c olonies larger than 0.05 mm in diameter with an incidence of 0.73 % an d 1.12 %, respectively. The lower incidence in TPA-exposed cultures ca n be interpreted in terms of TPA stimulation of keratinization. Howeve r, colonies larger than 0.1 mm in diameter were also developed by the TPA-exposed cells, indicating the presence of a cell population respon sive to promotional effects of TPA. These results imply that the cells involved in the formation of cystic squamous epithelial cell lesions are already initiated and possess a potential for autonomous benign gr owth.