Por favor, use este identificador para citar o enlazar este ítem: https://hdl.handle.net/20.500.12104/42178
Título: Increase of IFN-? and TNF-? production in CD107a + NK-92 cells co-cultured with cervical cancer cell lines pre-treated with the HO-1 inhibitor
Autor: Gomez-Lomeli, P.
Bravo-Cuellar, A.
Hernandez-Flores, G.
Jave-Suarez, L.F.
Aguilar-Lemarroy, A.
Lerma-Diaz, J.M.
Dominguez-Rodriguez, J.R.
Sanchez-Reyes, K.
Ortiz-Lazareno, P.C.
Fecha de titulación: 2014
Resumen: Background: Natural killer (NK) cells eliminate virus-infected and tumor cells through the release of perforins and granzymes; they also produce Interferon gamma (IFN-?) and Tumor necrosis factor alpha (TNF-?), which induce apoptosis in target cells. Many tumors express Heme oxygenase 1 (HO-1), and this expression has been associated with avoiding immunosuppression and apoptosis. In this work, HO-1+ Cervical cancer cell (CCC) lines were pre-treated with HO-1 inhibitor and we assessed whether this inhibition enhanced the sensitivity of CCC to NK cell activity.Methods: We assessed the expression of HO-1 in HeLa, SiHa, and C-33A CCC by Flow cytometry (FC). CCC were pre-treated with SnPP or ZnPP HO-1 inhibitors. After that, NK-92 cells were co-cultured with HeLa, SiHa, and C-33A CCC pre-treated or not with HO-1 inhibitors, and the expression of IFN-?, TNF-?, CD107a, Granzyme B, NKp44, NKp46, NKp30, and NKG2D was evaluated by FC. Results: CCC lines HeLa, SiHa, and C-33A expressed HO-1. Inhibition of HO-1 in these cells increased the expression of IFN-? and TNF-? in CD107a + NK-92 cells. We observed a reduction in the expression of NKG2D, NKp46, and NKp30 in NK cells co-cultured with HeLa and SiHa cells, and when HeLa and SiHa cells were pre-treated with the HO-1 inhibitors, the expression of NKG2D and NKp30 in NK cells was restored. We observed a similar effect in NK cells co-cultured with C-33A cells in NKp30 expression.Conclusion: Inhibition of HO-1 in CCC induces an increase in IFN-? and TNF-? production in CD107a + NK-92 cells and restores NKG2D, NKp46 and NKp30 downmodulation in NK cells. 2014 Gómez-Lomeli et al.; licensee BioMed Central Ltd.
URI: http://www.scopus.com/inward/record.url?eid=2-s2.0-84908095205&partnerID=40&md5=1be4eb27ef2c16bf70694d5add4546cc
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