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Updated: Jun 3, 2026

Experimental Infection with Listeria monocytogenes as a Model for Studying Host Interferon-γ Responses
Published on: November 16, 2016
[Interferon gamma-mediated growth regulation of epithelial cells]
Insights
Interferon gamma (IFNgamma) inhibits proliferation in epithelial cells with high epidermal growth factor receptor (EGFR) expression, but not those with low EGFR. This suggests EGFR levels are crucial for IFNgamma
Area of Science:
- Cell Biology
- Immunology
- Molecular Biology
Background:
- Interferon gamma (IFNgamma) is known to inhibit proliferation in certain transformed cell lines.
- Previous studies demonstrated IFNgamma-induced transactivation of epidermal growth factor receptor (EGFR) and its dependence on EGFR expression levels.
Purpose of the Study:
- To investigate the antiproliferative effect of IFNgamma on human epithelial cell lines with varying EGFR expression levels (A431, HeLa - high EGFR; HEK293 - low EGFR).
- To characterize IFNgamma-induced changes in cell growth, cell cycle, and apoptosis.
Main Methods:
- Cell counting and MTT assays to assess cell growth.
- Flow cytometry to analyze cell cycle distribution.
- Caspase 3 activation assays to detect apoptosis.
Main Results:
- IFNgamma inhibited cell growth in A431 and HeLa cells but not in HEK293 cells.
- IFNgamma treatment disturbed cell cycle progression in A431 and HeLa cells, with no effect on HEK293 cells.
- IFNgamma induced caspase 3 activation in A431 cells, indicating apoptosis involvement.
Conclusions:
- IFNgamma exhibits an antiproliferative effect on epithelial cells that is dependent on high EGFR expression.
- EGFR expression levels significantly influence the cellular response to IFNgamma, affecting growth, cell cycle, and apoptosis.
Abstract:
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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