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3 protocols using lumikine mifn α

1

Measuring Cytokine Responses in Immune Cells

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For cytokine measurement in culture supernatants, 1 × 106 total BMDCs, 5 × 104 FACS-purified pDCs, 1 × 105 CAL-1 or 3 × 106 PBMCs were left untreated or pre-treated for 1 h with the SFKs inhibitor PP2 (EMD Millipore), the inhibitor bafetinib (Adooq, Irvine, CA, USA) or the equivalent concentration of DMSO control, followed by 15 h in media in presence or absence of 0.1 μM CpG-B ODN 1668 (Roche), 1 μM CpG-A ODN 2216, 100 μM loxoribine (mouse cells) or 1 μg ml−1 R848 (human cells) (all from InvivoGen, San Diego, CA, USA).
Mouse type I IFN bioactivity was measured with reference to a recombinant mouse IFN-β standard (Research Diagnostics, Concord, MA, USA) using a L-929 cell line transfected with an interferon-sensitive luciferase. Human type I IFN bioactivity was measured with reference to a recombinant human IFN-β standard (InvivoGen) using HEK-Blue IFN-α/β cell line (InvivoGen). Mouse serum IFN-α, mouse and human TNF were measured, respectively, by luminescent ELISA (LumiKine mIFN-α, InvivoGen) or by ELISA (Mouse TNF-α ELISA Ready-SET-Go!, eBioscience, and Human TNF-α ELISA MAX, Biolegend) as described in the manufacturer's protocol.
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2

IFN Response Induction Protocol

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To induce an IFN response in vivo, Etv6flox/floxR26CreER/+ or control mice were treated with tamoxifen as described above. 9 d after the last treatment, mice were injected intravenously with 5 µg of CpG-A (ODN 2216; InvivoGen) complexed with DOTAP (30 µl DOTAP/100 µl total volume; Roche), and blood was collected 6 h later by cardiac puncture. IFN-α concentration in the sera was determined by ELISA (LumiKine mIFN-α; InvivoGen) according to the manufacturer’s recommendations.
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3

Measuring Cytokine Levels in pDCs

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For cytokine measurement in culture supernatants, spleen or BM cells from individual mice in the same group were pooled prior to FACS purification. FACS-purified pDCs (3 × 104 cells/well) were incubated in 120ul RPMI-1640 supplemented with 10% (vol/vol) fetal bovine serum, L-glutamine, penicillin-streptomycin, and HEPES pH 7.2) supplemented with 50μM β-mercaptoethanol in the presence or absence of CpG-B 1668 (Integrated DNA Technologies) at 0.1μM (Flt3L culture-derived pDC) or 1μM (splenic and BM pDC) or CpG-A 1585 (InvivoGen) at 0.5uM for 6 or 15 hours at 37°C. Supernatants were collected and stored at −80°C until further analysis. IFN-I bioactivity was measured with reference to a recombinant mouse IFNβ standard (Sigma-Aldrich) using ISRE-L929 reporter cells (L-929 cell line transfected with an interferon-sensitive luciferase) (Jiang et al., 2005 (link)). IFNα and IFNβ were measured by Lumikine mIFNα and Lumikine Xpress mIFNβ ELISA (InvivoGen), respectively, following manufacturer instructions. TNFα was measured by Mouse TNF alpha ELISA Ready-SET-Go!® (eBioscience) following manufacturer instructions. Graphs depicting cytokine measurements in this paper represent individual wells of stimulation.
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