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Transformed human bronchial epithelial cells (beas-2b) alter the growth and morphology of normal human bronchial epithelial cells in vitro
Authors:Craig D. Albright  Raymond T. Jones  Eric A. Hudson  Joseph A. Fontana  Benjamin F. Trump  James H. Resau
Affiliation:(1) Department of Pathology, Human Tissue Resource, University of Maryland School of Medicine, 22 South Greene Street, 21201 Baltimore, Maryland;(2) University of Maryland Cancer Center, University of Maryland School of Medicine, 22 South Greene Street, 21201 Baltimore, Maryland;(3) Department of Pathology, University of Maryland School of Medicine, 10 South Pine Street, 21201, MD, Baltimore, USA
Abstract:Normal human bronchial epithelial cells (BE) and adenovirus-12 SV40 hybrid virus transformed, non-tumorigenic human bronchial epithelial cells (BEAS-2B) were cultured for 7 days in a serum free hormone supplemented medium. BE cells after 3 days in culture were exposed to conditioned medium (CMt) from confluent BEAS-2B cells. By day 7, CMt-treated BE cells exhibited a lower colony forming efficiency (CFE), fewer cells per colony, and a reduced mitotic index (MI) and BrdU (bromodeoxyuridine) labeling index. CMt also enhanced the expression of a terminally differentiated squamous phenotype in BE cells. Cell free lysates from BEAS-2B cells (CFLt) had effects similar to CMt on the MI and morphology of BE cells. In contrast, CMt and CFLt did not inhibit the growth, or alter the morphology of BEAS-2B cells. Conditioned medium from BE cells (CMn) did not reduce the growth of BEAS-2B cells, and had little effect on the morphology of BE cells. In co-culturesAbbreviations BE normal bronchial epithelial cells - BEAS-2B adenovirus-12 SV40 hybrid virus transformed bronchial epithelial cells - CMn conditioned medium from BE cells - CMt conditioned medium from BEAS-2B cells - CFn cell free lysate from BE cells - CFLt cell free lysate from BEAS-2B cells - BrdU bromodeoxyuridine - KGM keratinocyte growth medium - TGF-beta transforming growth factor type beta - NCI-LHC National Cancer Institute-Laboratory of Human CarcinogenesisContribution No. 2801 from the Pathobiology Laboratory, University of Maryland.
Keywords:Bronchial epithelial cells  cell culture  communication  transforming growth factor-beta
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