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Research Article

An essential role for the interferon-inducible, double-stranded RNA-activated protein kinase PKR in the tumor necrosis factor-induced apoptosis in U937 cells

M C Yeung, J Liu, and A S Lau
PNAS October 29, 1996 93 (22) 12451-12455; https://doi.org/10.1073/pnas.93.22.12451
M C Yeung
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J Liu
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A S Lau
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Abstract

Tumor necrosis factor alpha (TNF-alpha) is well-characterized for its necrotic action against tumor cells; however, it has been increasingly associated with an apoptosis-inducing potential on target cells. While the signaling events and the actual cytolytic mechanism(s) for both TNF-alpha-induced necrosis and apoptosis remain to be fully elucidated, we report here on (i) the ability of TNF-alpha to induce apoptosis in the promonocytic U937 cells, (ii) the discovery of a cross-talk between the TNF-alpha and the interferon signaling pathways, and (iii) the pivotal role of interferon-inducible, double-stranded RNA-activated protein kinase (PKR) in the induction of apoptosis by TNF-alpha. Our data from microscopy studies, trypan blue exclusion staining, and apoptotic DNA ladder electrophoresis revealed that a subclone derived from U937 and carrying a PKR antisense expression vector was resistant to TNF-alpha-induced apoptosis. Further, TNF-alpha initiated a generalized RNA degradation process in which the participation of PKR was required. Finally, the PKR gene is a candidate "death gene" since overexpression of this gene could bring about apoptosis in U937 cells.

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An essential role for the interferon-inducible, double-stranded RNA-activated protein kinase PKR in the tumor necrosis factor-induced apoptosis in U937 cells
M C Yeung, J Liu, A S Lau
Proceedings of the National Academy of Sciences Oct 1996, 93 (22) 12451-12455; DOI: 10.1073/pnas.93.22.12451

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An essential role for the interferon-inducible, double-stranded RNA-activated protein kinase PKR in the tumor necrosis factor-induced apoptosis in U937 cells
M C Yeung, J Liu, A S Lau
Proceedings of the National Academy of Sciences Oct 1996, 93 (22) 12451-12455; DOI: 10.1073/pnas.93.22.12451
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Proceedings of the National Academy of Sciences: 116 (50)
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