Interferon-gamma induces ice gene expression and enhances cellular susceptibility to apoptosis in the U937 leukemia cell line

被引:103
作者
Tamura, T [1 ]
Ueda, S [1 ]
Yoshida, M [1 ]
Matsuzaki, M [1 ]
Mohri, H [1 ]
Okubo, T [1 ]
机构
[1] YOKOHAMA CITY UNIV,SCH MED,DIV BLOOD TRANSFUS,KANAZAWA KU,YOKOHAMA,KANAGAWA 236,JAPAN
关键词
D O I
10.1006/bbrc.1996.1752
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The roles of interferons (IFNs) in apoptosis are not fully understood. Zn this study we show that in the U937 monoblastic leukemia cell line, pretreatment with IFN-gamma enhanced sensitivity to apoptosis triggered by gamma-irradiation or antitumor agents (etoposide or adriamycin), as well as by anti-Fas antibody. In addition, IFN-gamma caused an increased expression of the interleukin-1 beta-converting enzyme (Ice) gene, following strong induction of the interferon regulatory factor-1 (IRF-1) gene, the product of which is a transcriptional activator of the Ice gene. An inhibitor of ICE/Ced-3 family proteases, Z-Asp-CH2-DCB, blocked apoptosis in control cells as well as in IFN-gamma-pretreated cells. These results suggest that enhanced susceptibility of IFN-gamma-pretreated cells to apoptosis is mediated through the induction of Ice by IRF-1. This pathway is not affected by interleukin-1 beta (IL-1 beta) since neutralizing antibody against IL-1 beta failed to suppress the IFN-gamma-mediated enhancement of cell death, and IL-1 beta itself did not mimic the effect of IFN-gamma. (C) 1996 Academic Press, Inc.
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页码:21 / 26
页数:6
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