The orphan nuclear receptor RORα is a negative regulator of the inflammatory response

被引:241
作者
Delerive, P
Monté, D
Dubois, G
Trottein, F
Fruchart-Najib, J
Mariani, J
Fruchart, JC
Staels, B
机构
[1] Inst Pasteur, INSERM, U325, Dept Atherosclerose, F-59019 Lille, France
[2] Univ Lille 2, Fac Pharm, F-59000 Lille, France
[3] Inst Biol Lille, UMR 8526, F-59019 Lille, France
[4] Inst Pasteur, INSERM, U167, F-59019 Lille, France
[5] Univ Paris 06, CNRS, UMR 7624, F-75005 Paris, France
关键词
D O I
10.1093/embo-reports/kve007
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Retinoid-related orphan receptor alpha (ROR alpha) (NR1F1) is a member of the nuclear receptor superfamily whose biological functions are largely unknown. Since staggerer mice, which carry a deletion in the ROR alpha gene, suffer from immune abnormalities, we generated an adenovirus encoding ROR alpha1 to investigate its potential role in control of the inflammatory response. We demonstrated that ROR alpha is expressed in human primary smooth-muscle cells and that ectopic expression of ROR alpha1 inhibits TNF alpha -induced IL-6, IL-8 and COX-2 expression in these cells. ROR alpha1 negatively interferes with the NF-kappaB signalling pathway by reducing p65 translocation as demonstrated by western blotting, immunostaining and electrophoretic mobility shift assays. This action of ROR alpha1 on NF-kappaB is associated with the induction of I kappaB alpha, the major inhibitory protein of the NF-kappaB signalling pathway, whose expression was found to be transcriptionally upregulated by ROR alpha1 via a ROR response element in the I kappaB alpha promoter. Taken together, these data identify ROR alpha1 as a potential target in the treatment of chronic inflammatory diseases, including atherosclerosis and rheumatoid arthritis.
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页码:42 / 48
页数:7
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