RA-inducible gene-I induction augments STAT1 activation to inhibit leukemia cell proliferation

RA-inducible gene I (RIG-I/DDX58) has been shown to activate IFN-β promoter stimulator 1 (IPS-1) on recognizing cytoplasmic viral RNAs. It is unclear how RIG-I functions within the IFN and/or RA signaling process in acute myeloid leukemia (AML) cells, however, where obvious RIG-I induction is observ...

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Veröffentlicht in:Proceedings of the National Academy of Sciences - PNAS 2011-02, Vol.108 (5), p.1897-1902
Hauptverfasser: Jiang, Lin-Jia, Zhang, Nan-Nan, Ding, Fei, Li, Xian-Yang, Chen, Lei, Zhang, Hong-Xin, Zhang, Wu, Chen, Sai-Juan, Wang, Zhu-Gang, Li, Jun-Min, Chen, Zhu, Zhu, Jiang
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Sprache:eng
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Zusammenfassung:RA-inducible gene I (RIG-I/DDX58) has been shown to activate IFN-β promoter stimulator 1 (IPS-1) on recognizing cytoplasmic viral RNAs. It is unclear how RIG-I functions within the IFN and/or RA signaling process in acute myeloid leukemia (AML) cells, however, where obvious RIG-I induction is observed. Here, we show that the RIG-I induction functionally contributes to IFN-α plus RA-triggered growth inhibition of AML cells. Interestingly, although RIG-I induction itself is under the regulation of STAT1, a major IFN intracellular signal mediator, under circumstances in which it does not stimulate IPS-1, it conversely augments STAT1 activation to induce IFN-stimulatory gene expression and inhibit leukemia cell proliferation. Thus, our results unveil a previously undescribed RIG-I activity in regulating the cellular proliferation of leukemia cells via STAT1, which is independent of its classic role of sensing viral invasion to trigger type I IFN transcription.
ISSN:0027-8424
1091-6490
DOI:10.1073/pnas.1019059108