Genistein regulates the IL-1 beta induced activation of MAPKs in human periodontal ligament cells through G protein-coupled receptor 30

被引:49
作者
Luo, Li-Jun [2 ,3 ]
Liu, Feng [3 ]
Lin, Zhi-Kai [1 ]
Xie, Yu-Feng [1 ]
Xu, Jia-Li [2 ]
Tong, Qing-Chun [2 ]
Shu, Rong [1 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Med, Shanghai Peoples Hosp 9, Dept Periodontol, Shanghai 200011, Peoples R China
[2] Shanghai Jiading Cent Hosp, Dept Stomatol, Shanghai 201800, Peoples R China
[3] Shanghai Jiao Tong Univ, Sch Med, Chinese Acad Sci, Shanghai Inst Biol Sci,Inst Hlth Sci,Lab Signal T, Shanghai 200025, Peoples R China
关键词
Mitogen-activated protein kinases (MAPKs); Periodontal ligament cell; Genistein; G protein-coupled receptors 30 (GPR30); Interleukin-1; beta; UP-REGULATION; SIGNALING PATHWAYS; CANCER CELLS; EXPRESSION; GPR30; GROWTH; REQUIRES; BETA; 17-BETA-ESTRADIOL; PROLIFERATION;
D O I
10.1016/j.abb.2012.04.007
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
Periodontal ligament (PDL) cells are fibroblasts that play key roles in tissue integrity, periodontal inflammation and tissue regeneration in the periodontium. The periodontal tissue destruction in periodontitis is mediated by host tissue-produced inflammatory cytokines, including interleukin-1 beta (IL-1 beta). Here, we report the expression of G protein-coupled receptor 30 (GPR30, also known as G protein-coupled estrogen receptor 1 GPER) in human PDL cells and its regulation by IL-1 beta. IL-1 beta-induced GPR30 expression in human PDL cells leads to the activation of multiple signaling pathways, including MAPK, NF-kappa B and PI3K. In contrast, genistein, an estrogen receptor ligand, postpones the activation of MAPKs induced by IL-1 beta. Moreover, the inhibition of GPR30 by G15, a GPR30-specific antagonist, eliminates this delay. Thus, genistein plays a role in the regulation of MAPK activation via GPR30, and GPR30 represents a novel target regulated by steroid hormones in PDL cells. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:9 / 16
页数:8
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