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- Title
Functional Crosstalk between Type I and II Interferon through the Regulated Expression of STAT1.
- Authors
Gough, Daniel J.; Messina, Nicole L.; Hii, Linda; Gould, Jodee A.; Kanaga6Sabapathy; Robertson, Ashley P. S.; Trapani, Joseph A.; Levy, David E.; Hertzog, Paul J.; Clarke, Christopher J. P.; Johnstone, Ricky W.
- Abstract
Autocrine priming of cells by small quantities of constitutively produced type I interferon (IFN) is a well-known phenomenon. In the absence of type I IFN priming, cells display attenuated responses to other cytokines, such as anti-viral protection in response to IFNc. This phenomenon was proposed to be because IFNa/b receptor1 (IFNAR1) is a component of the IFNc receptor (IFNGR), but our new data are more consistent with a previously proposed model indicating that regulated expression of STAT1 may also play a critical role in the priming process. Initially, we noticed that DNA binding activity of STAT1 was attenuated in c-Jun-/- fibroblasts because they expressed lower levels of STAT1 than wild-type cells. However, expression of STAT1 was rescued by culturing c-Jun-/- fibroblasts in media conditioned by wild-type fibroblasts suggesting they secreted a STAT1-inducing factor. The STAT1-inducing factor in fibroblast-conditioned media was IFNb, as it was inhibited by antibodies to IFNAR1, or when IFNb expression was knocked down in wild-type cells. IFNAR1-/- fibroblasts, which cannot respond to this priming, also expressed reduced levels of STAT1, which correlated with their poor responses to IFNc. The lack of priming in IFNAR1-/- fibroblasts was compensated by over-expression of STAT1, which rescued molecular responses to IFNc and restored the ability of IFNc to induce protective anti-viral immunity. This study provides a comprehensive description of the molecular events involved in priming by type I IFN. Adding to the previous working model that proposed an interaction between type I and II IFN receptors, our work and that of others demonstrates that type I IFN primes IFNc-mediated immune responses by regulating expression of STAT1. This may also explain how type I IFN can additionally prime cells to respond to a range of other cytokines that use STAT1 (e.g., IL-6, M-CSF, IL-10) and suggests a potential mechanism for the changing levels of STAT1 expression observed during viral infection.
- Subjects
INTERFERONS; ANTIVIRAL agents; TRANSCRIPTION factors; VIRUS diseases; CYTOKINES; GENE expression
- Publication
PLoS Biology, 2010, Vol 8, Issue 4, p1
- ISSN
1544-9173
- Publication type
Article
- DOI
10.1371/journal.pbio.1000361