Titanium induced production of chemokines CCL17/TARC and CCL22/MDC in human osteoclasts and osteoblasts

被引:45
作者
Cadosch, Dieter [1 ,2 ]
Gautschi, Oliver P. [1 ,2 ]
Chan, Erwin [1 ]
Simmen, Hans-Peter [3 ]
Filgueira, Luis [1 ]
机构
[1] Univ Western Australia, Sch Anat & Human Biol, Crawley, WA, Australia
[2] Royal Perth Hosp, Dept Traumat & Orthopaed Surg, Perth, WA, Australia
[3] Univ Zurich Hosp, Div Trauma Surg, CH-8091 Zurich, Switzerland
关键词
titanium; osteoclast; osteoblast; CCL17; CCL22; TOTAL HIP-ARTHROPLASTY; BONE-RESORPTION; WEAR PARTICLES; CELL-ACTIVATION; IN-VITRO; DIFFERENTIATION; REPLACEMENT; LYMPHOCYTE; RECEPTORS; CYTOKINES;
D O I
10.1002/jbm.a.32390
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
There is increasing evidence that titanium (Ti(IV)) ions are released from orthopedic implants and play a role in aseptic loosening. This Study aimed to investigate whether titanium induces expression of chemokines and cytokines that are important in osteoclastogenesis in human osteoclasts and osteoblasts. Incubation of those cells with 1 mu M Ti(IV) significantly upregulated expression of CCL17/TARC and CCL22/MDC, RANK-L, M-CSF and pro-inflammatory cytokines as determined by quantitative real-time PCR and ELISA assays. Additionally, flow cytometry was used to show Ti(IV) related increased expression of CCR4, the cognate receptor for CCL17 and CCL22 in challenged osteoclast precursors. These results strongly suggest that Ti(IV) ions play a role in the recruitment of osteoclast precursors to the bone-implant interface by increasing CCL17 and CCL22 expression and by upregulating their cognate receptor. Moreover the increased expression of RANK-L and M-CSF by osteoblasts together with increased levels of pro-inflammatory cytokines may enhance osteoclast differentiation and activity, and subsequently contribute to the pathomechanism of aseptic loosening. (C) 2009 Wiley Periodicals, Inc. J Biomed Mater Res 92A: 475-483, 2010
引用
收藏
页码:475 / 483
页数:9
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