Basic Information
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Description
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- IFNAR1, together with IFNAR2, forms the heterodimeric receptor for type I interferons. After binding with type I interferons, the IFNAR1/IFNAR2 receptor activates the JAK-STAT signaling cascade, which results in the transcriptional activation or repression of interferon-regulated genes.
- The knock-out mice developed normally.
- This model is useful in studying the role of IFN pathways in anti-viral and anti-microbial infections.
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Targeting strategy
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Gene targeting strategy for B-Ifnar1 KO mice(129S2). The genome sequences between exons 1-11 in mouse Ifnar1 gene were depleted in B-Ifnar1 KO mice(129S2). As a result, mouse IFNAR1 protein will not be expressed anymore.
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mRNA expression analysis
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Strain specific analysis of Ifnar1 mRNA expression in wild-type 129S2 mice and B-Ifnar1 KO mice(129S2) by RT-PCR. Spleen RNA were isolated from wild-type 129S2 mice (+/+) and homozygous B-Ifnar1 KO mice(129S2) (-/-), then cDNA libraries were synthesized by reverse transcription, followed by PCR with mouse Ifnar1 primers. Mouse Ifnar1 mRNA was only detectable in wild-type mice, but not in B-Ifnar1 KO mice(129S2).
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Protein expression analysis in spleen
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IFNAR1 expression analysis in wild-type 129S2 mice and homozygous B-Ifnar1 KO mice(129S2) by flow cytometry. Spleen were collected from wild-type 129S2 mice (+/+) and homozygous B-Ifnar1 KO mice(129S2) (-/-). Protein expression was analyzed with anti-mouse IFNAR1 antibody (Biolegend, 127311) by flow cytometry. Wild-type C57BL/6N mice was used as a positive control for analysis. Mouse IFNAR1 was detectable in granulocytes, DC cells, B cells and macrophages from wild-type 129S2 mice, but not in those cell types from B-Ifnar1 KO mice(129S2).
Ifnar1 expression analysis in wild-type 129S2 mice and homozygous B-Ifnar1 KO mice(129S2) by flow cytometry. Spleen were collected from wild-type 129S2 mice (+/+) and homozygous B-Ifnar1 KO mice(129S2) (-/-). Protein expression was analyzed with anti-mouse Ifnar1 antibody (Biolegend, 127311) by flow cytometry. Wild-type C57BL/6N mice was used as a positive control for analysis. Mouse IFNAR1 was detectable monocytes, T cells and NK cells from wild-type 129S2 mice, but not in those cell types from B-Ifnar1 KO mice(129S2).
