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[Interferon gamma-mediated growth regulation of epithelial cells].
Tsitologiia ; 52(12): 977-82, 2010.
Article en Ru | MEDLINE | ID: mdl-21427975
Interferon gamma (IFNgamma) is known to inhibit proliferation of certain transformed cell lines. Recently, we have demonstrated the transactivation of the epidermal growth factor receptor (EGFR) in response to IFNgamma (Burova et al., 2007) and provided direct evidence for the dependence of IFNgamma-induced EGFR transactivation upon EGFR expression level in epithelial cells (Gonchar et al., 2008). This study examines an antiproliferative effect of IFNgamma on human epithelial cells lines A431 and HeLa which express high levels of EGFR, as well as HEK293, which expresses low levels of EGFR. We characterized the IFNgamma-induced changes in these cells by studying cell growth, the cell cycle and induction of apoptosis. The response to IFNgamma differed in the tested cell lines: cell growth was inhibited in both A431 and HeLa cells, but not in HEK293 cells, as shown by cell counts and MTT. The cell cycle phases analyzed by flow cytometry were disturbed in A431 and HeLa cells in response to IFNgamma. In contrast, IFNgamma treatment did not alter distribution by cell cycle phases in HEK293. Our results indicate that IFNgamma exhibit an antiproliferative effect depending on the increased expression of EGFR in A431 and HeLa cells. Further, it was demonstrated that IFNgamma induced the caspase 3 activation in A431 cells, suggesting an involvement of active caspase 3 in IFNgamma-induced apoptosis.
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Antivirales / Interferón gamma / Apoptosis / Proliferación Celular / Células Epiteliales Límite: Humans Idioma: Ru Revista: Tsitologiia Año: 2010 Tipo del documento: Article Pais de publicación: Rusia
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Antivirales / Interferón gamma / Apoptosis / Proliferación Celular / Células Epiteliales Límite: Humans Idioma: Ru Revista: Tsitologiia Año: 2010 Tipo del documento: Article Pais de publicación: Rusia