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|Type:||Artigo de periódico|
|Title:||The effect of IFN-gamma and TNF-alpha on the NADPH oxidase system of human colostrum macrophages, blood monocytes, and THP-1 cells|
|Abstract:||The aim of this work was to analyze the effect of Interferon-gamma ( IFN-gamma) and tumor necrosis factor-alpha ( TNF-alpha) on NADPH oxidase activity and gp91- phox gene expression in human colostrum macrophages ( CM), peripheral blood monocytes ( PBM), and myelomonocytic THP- 1 cells. We also investigated the effect of IFN-gamma on the release of TNF-alpha by these cells. Our results show that under basal culture conditions, CM release more superoxide than PBM and THP- 1 cells ( p < 0.05). The addition of IFN-gamma, alone or in combination with TNF-alpha, increased spontaneous superoxide release by PBM and THP- 1 cells ( p < 0.05) and increased phorbol myristate acetate ( PMA)- stimulated superoxide release by CM, PBM, and THP- 1 cells ( p < 0.05). The NADPH oxidase activity of THP- 1 cells consistently remained lower than that of CM or PBM, despite a dramatic response to IFN-gamma and TNF-alpha. Under basal conditions, gp91- phox gene expression was significantly higher in CM and PBM compared with THP- 1 cells ( p < 0.05). The addition of IFN-gamma alone or in combination with TNF-alpha caused a dramatic increase in gp91- phox gene expression in THP- 1 cells ( p < 0.05) but not in CM or PBM. Under basal conditions or in the presence of IFN-gamma, CM released more TNF-alpha than PBM or THP- 1 cells ( p < 0.05). In addition, PBM released more TNF-alpha than THP- 1 cells ( p < 0.05). IFN-gamma did not significantly augment the release of TNF-alpha by these cells ( p > 0.05). Thus, IFN-gamma and TNF-alpha induced equivalent gp91- phox gene expression in THP- 1 cells compared with CM or PBM but did not bring about equivalent NADPH oxidase activity. TNF-alpha release was higher in more mature cells. This partial divergence of gp91-phox gene expression, NADPH oxidase activity, and TNF-alpha release is probably a consequence of different events of myeloid cell biology and relates at least in part to cell differentiation state.|
|Editor:||Mary Ann Liebert Inc|
|Appears in Collections:||Unicamp - Artigos e Outros Documentos|
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