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Type I interferons are essential mediators of apoptotic death in virally infected cells
Author(s) -
Tanaka Nobuyuki,
Sato Mitsuharu,
Lamphier Marc S.,
Nozawa Hiroaki,
Oda Eri,
Noguchi Shigeru,
Schreiber Robert D.,
Tsujimoto Yoshihide,
Taniguchi Tadatsugu
Publication year - 1998
Publication title -
genes to cells
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.912
H-Index - 115
eISSN - 1365-2443
pISSN - 1356-9597
DOI - 10.1046/j.1365-2443.1998.00164.x
Subject(s) - biology , apoptosis , interferon , programmed cell death , immunology , virology , interferon type i , microbiology and biotechnology , genetics
Background The interferons (IFNs) have been extensively studied in the context of host defence against viral infection. In the established model of IFN action, virally infected cells secrete type I IFNs (IFN‐α/β) which induce an antiviral state in uninfected cells. However, it is not clear how IFNs function on the infected cells. It has been reported that cells infected by some viruses die by apoptosis. Results In the present study, we found that three types of viruses commonly induce apoptosis in primary cell cultures. Importantly, we observed that virus‐induced apoptosis was inhibited by anti‐IFN‐α/β antibodies, and in cells lacking either the type I IFN receptor 1 (IFNAR1) or its downstream mediator, Stat1 (Signal transducer and activator of transcription 1). IFN‐α treatment by itself did not induce apoptosis unless it was combined with transfection by double‐stranded RNA (dsRNA), which is normally generated during the course of viral infection. Conclusion These results indicate a novel antiviral function of the type I IFNs, i.e. the selective induction of apoptosis in virally infected cells. In effect, these IFNs have a bifunctional role in limiting the spread of virus; eliciting an antiviral state in uninfected cells while promoting apoptosis in infected cells. Our results may help explain why IFNs are sometimes useful in the treatment of viral diseases and will provide further insight into the mechanisms of virus‐induced pathogenesis

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