Upregulation of TLR2 expression is induced by estrogen via an estrogen-response element (ERE)

被引:13
作者
Li, Xi [1 ,3 ]
Li, Miao [2 ]
Bai, Xizhuang [3 ]
机构
[1] China Med Univ, Affiliated Hosp 4, Dept Orthoped Surg, Shenyang 110032, Peoples R China
[2] China Med Univ, Coll Basic Med Sci, Dept Pathogen Biol, Shenyang 110001, Peoples R China
[3] China Med Univ, Affiliated Hosp 1, Dept Sports Med & Joint Surg, Shenyang 110001, Peoples R China
关键词
TLR2; Gene expression; 17; beta-Estradiol; ERE; EARLY RHEUMATOID-ARTHRITIS; RECEPTORS; PATHWAYS; BINDING; CELLS;
D O I
10.1016/j.abb.2014.01.028
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
TLR2 and estrogen are both thought to be involved in the pathogenesis of RA; however, it is unknown if there is an association between estrogen and TLR2. In this report, we treated PMA-differentiated THP-1 cells with 17 beta-estradiol (E2) and observed increases in TLR2 mRNA and protein levels by real-time quantitative PCR and western blot. Transfection of THP-1 cells with a series of 5 '-deleted TLR2 promoter-luciferase constructs revealed that E2 enhanced TLR2 transcriptional activity in an estrogen receptor alpha (ERot)-dependent pattern. An estrogen receptor response element (ERE) was identified 251 bases upstream of the TLR2 promoter, and electrophoretic mobility shift assay and chromatin immunoprecipitations showed ER alpha binding was increased by E2. In summary, this work demonstrated that TLR2 is a new estrogen-regulated gene whose expression is upregulated through the interaction of ERot with an ERE in the promoter region. (C) 2014 Published by Elsevier Inc.
引用
收藏
页码:26 / 31
页数:6
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