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NFATC3 promotes IRF7 transcriptional activity in plasmacy--toid dendritic cells.
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- Additional Information
- Source:
Publisher: Rockefeller University Press Country of Publication: United States NLM ID: 2985109R Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1540-9538 (Electronic) Linking ISSN: 00221007 NLM ISO Abbreviation: J Exp Med Subsets: MEDLINE
- Publication Information:
Original Publication: New York, NY : Rockefeller University Press
- Subject Terms:
- Abstract:
Plasmacytoid dendritic cells (pDCs) rapidly produce large amounts of type 1 interferon (IFN) after Toll-like receptor 7 and 9 engagements. This specialized function of type 1 IFN production is directly linked to the constitutive expression of IRF7, the master transcription factor for type 1 IFN production. However, the IRF7 regulatory network in pDCs remains largely unknown. In this study, we identify that the transcription factor NFATC3 specifically binds to IRF7 and enhances IRF7-mediated IFN production. Furthermore, knockout of NFATC3 greatly reduced the CpG DNA-induced nuclear translocation of IRF7, which resulted in impaired type 1 IFN production in vitro and in vivo. In addition, we found that NFATC3 and IRF7 both bound to type 1 IFN promoters and that the NFAT binding site in IFN promoters was required for IRF7-mediated IFN expression. Collectively, our study shows that the transcription factor NFATC3 binds to IRF7 and functions synergistically to enhance IRF7-mediated IFN expression in pDCs.
(© 2016 Bao et al.)
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- Accession Number:
0 (CPG-oligonucleotide)
0 (IRF7 protein, human)
0 (Interferon Regulatory Factor-7)
0 (Interferon Type I)
0 (Irf7 protein, mouse)
0 (NFATC Transcription Factors)
0 (Oligodeoxyribonucleotides)
0 (transcription factor NF-AT c3)
- Publication Date:
Date Created: 20161005 Date Completed: 20170731 Latest Revision: 20181113
- Publication Date:
20231215
- Accession Number:
PMC5068237
- Accession Number:
10.1084/jem.20160438
- Accession Number:
27697837
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