Cutting edge: Autoantigen Ro52 is an interferon inducible E3 ligase that ubiquitinates IRF-8 and enhances cytokine expression in macrophages

被引:161
作者
Kong, Hee Jeong
Anderson, D. Eric
Lee, Chang Hoon
Jang, Moon Kyoo
Tamura, Tomohiko
Tailor, Prafullakumar
Cho, Hyun Kook
Cheong, JaeHun
Xiong, Huabao
Morse, Herbert C., III
Ozato, Keiko
机构
[1] NICHHD, Lab Mol Growth Regulat, GDP, NIH, Bethesda, MD 20892 USA
[2] NIDDKD, Proteom & Mass Spectrometry Facil, NIH, Bethesda, MD USA
[3] NIAID, Immunopathol Lab, NIH, Bethesda, MD 20892 USA
[4] Natl Fisheries Res & Dev Inst, Biotechnol Res Inst, Pusan, South Korea
[5] Mt Sinai Sch Med, Immunobiol Ctr, New York, NY 10029 USA
关键词
D O I
10.4049/jimmunol.179.1.26
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
IFN regulatory factor (IRF)-8 is a transcription factor important for the development and function of macrophages. It plays a critical role in the induction of cytokine genes, including IL-12p40. Immunopurification and mass spectrometry analysis found that IRF-8 interacted with Ro52 in murine macrophages upon IFN-gamma and TLR stimulation. Ro52 is an IFN-inducible protein of the tripartite motif (TRIM) family and is an autoantigen present in patients with Sjogren's syndrome and systemic lupus erythematosus. Ro52 has a RING motif and is capable of ubiquitinating itself. We show that IRF-8 is ubiquitinated by Ro52 both in vivo and in vitro. Ectopic expression of Ro52 enhanced IL-12p40 expression in IFN-gamma/TLR-stimulated macrophages in an IRF-8-dependent manner. Together, Ro52 is an E3 ligase for IRF-8 that acts in a non-degradation pathway of ubiquitination, and contributes to the elicitation of innate immunity in macrophages.
引用
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页码:26 / 30
页数:5
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