Effects of polyethylene and TiAlV wear particles on expression of RANK, RANKL and OPG mRNA

被引:35
|
作者
Baumann, B [1 ]
Rader, CP
Seufert, J
Nöth, U
Rolf, O
Eulert, J
Jakob, F
机构
[1] Univ Wurzburg, Konig Ludwig Haus, Dept Orthoped Surg, Wurzburg, Germany
[2] Univ Wurzburg, Med Poliklin, Dept Metab Endocrinol & Mol Med, Wurzburg, Germany
来源
ACTA ORTHOPAEDICA SCANDINAVICA | 2004年 / 75卷 / 03期
关键词
D O I
10.1080/00016470410001222
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
Background Wear debris has been associated with periprosthetic osteolysis and loosening of total joint arthroplasties. RANKL (receptor activator of NF-kappaB ligand), RANK (receptor activator of NF-kappaB) and OPG (osteoprotegerin) are three key molecules which regulate differentiation, survival, fusion, and activation of osteoclasts. Material and methods We evaluated the effect of TiAlV and polyethylene particles on expression of RANK, RANKL and OPG mRNA. We used a human monocytic leukemic cell line (THP-1) in this in vitro study. THP-1 monocytes were differentiated into macrophage-like cells and exposed to polyethylene particles and prosthesis-derived TiAlV particles. The supernantant was used for measurement of TNFalpha protein and total RNA was extracted from the cells. Expression of the genes coding for OPG, RANKL and RANK was analysed at the mRNA level using a semiquantitative RT-PCR method. Results Both polyethylene and TiAlV particles induced a significant release of TNFalpha after 6 h of exposure and a significant upregulation of RANK mRNA. OPG mRNA expression was transiently upregulated after exposure to polyethylene and TiAlV particles. These effects were dependent on particle dose. RANKL mRNA was not detectable in our THP-1 model. In contrast, LPS exhibited a different pattern of RANK/ RANKL/OPG mRNA expression. Interpretation Our findings provide evidence that both polyethylene and TiAlV particles induce upregulation of RANK expression in cells of the monocytic lineage, which may be important for periprosthetic osteoclastogenesis.
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页码:295 / 302
页数:8
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