Suppression of Osteoblast Toll-Like Receptor 2 Signaling by Endothelin-1

被引:2
|
作者
Suzaki, Ai [1 ,2 ]
Komine-Aizawa, Shihoko [2 ]
Hayakawa, Satoshi [2 ]
机构
[1] Surugadai Nihon Univ Hosp, Dept Gen Med, Tokyo, Japan
[2] Nihon Univ, Sch Med, Div Microbiol, Dept Pathol & Microbiol, Tokyo, Japan
关键词
Endothelin-1; Toll-like receptor 2; NF-B; interleukin; 6; osteoblast; MURINE; INTERLEUKIN-6;
D O I
10.1002/jor.22627
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Peripheral endothelin-1 (ET-1) levels are increased in chronic systemic disorders such as congestive cardiac failure, diabetes and chronic renal failure. Bone infections are also associated with poor prognoses in these conditions. In the present study, we examined the alterations in Toll-like receptor 2 (TLR2) signaling induced by ET-1 in an in vitro osteoblast cell model. The TLR2-positive murine osteoblast cell line MC3T3-E1 was treated with heat-killed Listeria monocytogenes (HKLM), a TLR2 ligand, in the presence or absence of ET-1. We examined TLR2 expression, intranuclear NF-B phosphorylation and interleukin 6 (IL-6) production. ET-1 suppressed cell surface expression of TLR2, NF-B phosphorylation and IL-6 production. As TLR2 represents an important mechanism by which osteoblasts recognize bacterial pathogens, a continuously elevated ET-1 status may impair pathogenic recognition by osteoblasts and consequently affect bone metabolism during infections. (c) 2014 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 32:910-914, 2014.
引用
收藏
页码:910 / 914
页数:5
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