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Inhibitory effect of (-)-epigallocatechin gallate on titanium particle-induced TNF-${alpha}$ release and $in$ $vivo$ osteolysis
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  • Inhibitory effect of (-)-epigallocatechin gallate on titanium particle-induced TNF-${alpha}$ release and $in$ $vivo$ osteolysis
  • Inhibitory effect of (-)-epigallocatechin gallate on titanium particle-induced TNF-${alpha}$ release and $in$ $vivo$ osteolysis
저자명
Jin. Shan,Park. Ju-Young,Hong. Jung-Min,Kim. Tae-Ho,Shin. Hong-In,Park. Eui-Kyun,Kim. Shin-Yoon
간행물명
Experimental & molecular medicine : EMM
권/호정보
2011년|43권 7호|pp.411-418 (8 pages)
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생화학분자생물학회
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정기간행물|ENG|
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이 논문은 한국과학기술정보연구원과 논문 연계를 통해 무료로 제공되는 원문입니다.
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기타언어초록

Tumor necrosis factor-${alpha}$ (TNF-${alpha}$) and inflammatory cytokines released from activated macrophages in response to particulate debris greatly impact periprosthetic bone loss and consequent implant failure. In the present study, we found that a major polyphenolic component of green tea, (-)-epigallocatechin gallate (EGCG), inhibited Ti particle-induced TNF-${alpha}$ release in macrophages $in$ $vitro$ and calvarial osteolysis $in$ $vivo$. The Ti stimulation of macrophages released TNF-${alpha}$ in a dose- and time-dependent manner, and EGCG substantially suppressed Ti particle-induced TNF-${alpha}$ release. Analysis of signaling pathway showed that EGCG inhibited the Ti-induced c-Jun N-terminus kinase (JNK) activation and inhibitory ${kappa}B$ ($I{kappa}B$) degradation, and consequently the Ti-induced transcriptional activation of AP-1 and $NF-{kappa}B$. In a mouse calvarial osteolysis model, EGCG inhibited Ti particle-induced osteolysis $in$ $vivo$ by suppressing TNF-${alpha}$ expression and osteoclast formation. Therefore, EGCG may be a potential candidate compound for osteolysis prevention and treatment as well as aseptic loosening after total replacement arthroplasty.