Nuclear Receptor Retinoid-Related Orphan Receptor α1 Modulates the Metabolic Activity of Human Osteoblasts

被引:18
|
作者
Benderdour, Mohamed [1 ]
Fahmi, Hassan [2 ]
Beaudet, Francois [3 ]
Fernandes, Julio C. [1 ]
Shi, Qin [1 ]
机构
[1] Univ Montreal, Orthopaed Res Lab, Res Ctr, Hop Sacre Coeur Montreal, Montreal, PQ H4J 1C5, Canada
[2] Univ Montreal, Ctr Hosp, Res Ctr, Osteoarthrit Res Unit,Notre Dame Hosp, Montreal, PQ H4J 1C5, Canada
[3] Univ Montreal, Hop Sacre Coeur Montreal, Dept Rheumatol, Montreal, PQ H4J 1C5, Canada
关键词
ROR alpha 1; OSTEOBLAST METABOLISM MARKERS; INFLAMMATORY RESPONSES; AMINO-TERMINAL DOMAINS; FACTOR-KAPPA-B; GENE-EXPRESSION; ROR-ALPHA; RHEUMATOID-ARTHRITIS; IN-VITRO; BONE; CELLS; DIFFERENTIATION; ROR-ALPHA-1;
D O I
10.1002/jcb.23141
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
Nuclear receptor retinoid-related orphan receptor alpha (ROR alpha 1) is a member of ROR-family receptors. It is broadly expressed in various tissues and organs during embryonic development. However, so far, little is known about its function in bone. Here, we have elucidated the expression and function of ROR alpha 1 in human MG-63 osteoblast-like cells. Reverse transcriptase-polymerase chain reaction and immunocytochemical analysis revealed that human MG-63 osteoblasts expressed and produced ROR alpha 1. Other cell lines, such as THP-1 monocytes expressed also ROR alpha 1. ROR alpha 1 over-expression increased alkaline phosphatase, osteocalcin, cell mineralization, and collagen type I mRNA and protein expression, while ROR alpha 1 RNA silencing inhibited these responses. In addition, ROR alpha 1 over-expression suppressed the tumor necrosis factor-alpha (TNF alpha)-induced production of cyclooxygenase-2, prostaglandin E(2), and metalloproteinase-9. Examination of the signaling pathways disclosed that ROR alpha 1 was able to block TNF alpha-evoked nuclear factor-kappaB activation. In conclusion, this study demonstrates that ROR alpha 1 is involved in human osteoblast metabolism by stimulating osteoblast marker expression and inhibiting inflammatory responses. The results may encourage further exploration of ROR alpha 1 as a potential target for the treatment of bone disorders related to inflammation. J. Cell. Biochem. 112: 2160-2169, 2011. (C) 2011 Wiley-Liss, Inc.
引用
收藏
页码:2160 / 2169
页数:10
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