Chemokine gene activation in human bone marrow-derived osteoblasts following exposure to particulate wear debris

被引:54
作者
Fritz, EA
Glant, TT
Vermes, C
Jacobs, JJ
Roebuck, KA
机构
[1] Rush Univ, Med Ctr, Dept Orthoped Surg, Chicago, IL 60612 USA
[2] Rush Univ, Med Ctr, Dept Immunol & Microbiol, Chicago, IL 60612 USA
[3] Rush Univ, Med Ctr, Dept Biochem, Chicago, IL 60612 USA
关键词
wear debris; osteolysis; osteoblast; chemokine;
D O I
10.1002/jbm.a.30609
中图分类号
R318 [生物医学工程];
学科分类号
0831 [生物医学工程];
摘要
Particulate wear debris induces the expression of pro-inflammatory cytokine and chemokine genes in various cell types of the periprosthetic region. We have previously reported that titanium particles stimulate the selective induction of interleukin-8 (IL-8) and monocyte chemoattractant protein-1 (MCP-1) chemokines in human osteoblast-like osteosarcoma cells. In this study, we characterize the human bone marrow-derived osteoblast chemokine response to titanium particles. We demonstrate that titanium particles result in enhanced IL-8 and MCP-1 protein secretion as well as differential chemokine gene activation. Osteoblast chemokine expression was regulated at the level of gene transcription, with a tune-dependent induction of NF-kappa B activation. Inhibition studies with N-acetyl-L-cysteine (Nac) and MG-132 suggest that titanium particle activation of NF-kappa B activity and IL-8 chemokine exression involves oxidant signaling and I kappa B alpha-proteasomal degradation. Activation of the NF-kappa B transcription factor, as well as the IL-8 gene, are redox-regulated. We also demonstrate that while cytochalasin D, a potent inhibitor of phagocytosis, suppressed the titanium particle effect on IL-8 protein release in human bone marrow-derived osteoblasts, the inhibitor had no effect on IL-8 expression in MG-63 osteoblast-like cells. Collectively, these results provide insight into the potential mechanisms responsible for the particulate activation of osteoblast chemokine expression and suggest an important role for the osteoblast in the pathogenesis of periprosthetic osteolysis. (c) 2005 Wiley Periodicals, Inc.
引用
收藏
页码:192 / 201
页数:10
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