The transcriptional regulator NAB2 reveals a two-step induction of TRAIL in activated plasmacytoid DCs

被引:9
作者
Balzarolo, Melania [1 ,2 ]
Karrich, Julien J. [3 ]
Engels, Sander [1 ]
Blom, Bianca [3 ]
Medema, Jan Paul [2 ]
Wolkers, Monika C. [1 ,2 ]
机构
[1] Sanquin Res AMC Landsteiner Lab, Dept Hematopoiesis, NL-1066 CX Amsterdam, Netherlands
[2] Univ Amsterdam, Acad Med Ctr, CEMM, Lab Expt Oncol & Radiobiol LEXOR, NL-1105 AZ Amsterdam, Netherlands
[3] Univ Amsterdam, Acad Med Ctr, Dept Cell Biol & Histol, NL-1105 AZ Amsterdam, Netherlands
关键词
NAB2; Plasmacytoid DC; TRAIL expression; Type I IFN; INDUCED IFN-ALPHA; T-CELL FUNCTION; DENDRITIC CELLS; I INTERFERON; P38; MAPK; EXPRESSION; RECEPTOR; VIRUS; GENE; RESPONSES;
D O I
10.1002/eji.201242385
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Plasmacytoid dendritic cells (pDCs) are key players in antiviral immunity. In addition to massive type I interferon production, activated pDCs express the apoptosis-inducing molecule TRAIL, which enables them to clear infected cells that express the TRAIL receptors TRAIL-R1 and TRAIL-R2. In this study, we examined the molecular mechanisms that govern TRAIL expression in human pDCs. We identify NGFI-A-binding protein 2 (NAB2) as a novel transcriptional regulator that governs TRAIL induction in stimulated pDCs. We show with the pDC-like cell line CAL-1 that NAB2 is exclusively induced downstream of TLR7 and TLR9 signaling, and not upon type I IFN-R signaling. Furthermore, PI3K signaling is required for NAB2-mediated TRAIL expression. Finally, we show that TRAIL induction in CpG-activated human pDCs occurs through two independent signaling pathways: the first is initiated through TLR9 signaling upon recognition of nucleic acids, followed by type I IFN-R-mediated signaling. In conclusion, our data suggest that these two pathways are downstream of different activation signals, but act in concert to allow for full TRAIL expression in pDCs.
引用
收藏
页码:3019 / 3027
页数:9
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