Effects of Ti, PMMA, UHMWPE, and Co-Cr wear particles on differentiation and functions of bone marrow stromal cells

This study investigates the roles of orthopedic biomaterial particles [Ti‐alloy, poly(methyl methacrylate) (PMMA), ultrahigh‐molecular‐weight polyethylene (UHMWPE), Co–Cr alloy] on the differentiation and functions of bone marrow stromal cells (BMSCs). Cells were isolated from femurs of BALB/c mice...

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Published inJournal of biomedical materials research. Part A Vol. 101; no. 10; pp. 2817 - 2825
Main Authors Jiang, Yunpeng, Jia, Tanghong, Gong, Weiming, Wooley, Paul H., Yang, Shang-You
Format Journal Article
LanguageEnglish
Published Hoboken, NJ Blackwell Publishing Ltd 01.10.2013
Wiley-Blackwell
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Summary:This study investigates the roles of orthopedic biomaterial particles [Ti‐alloy, poly(methyl methacrylate) (PMMA), ultrahigh‐molecular‐weight polyethylene (UHMWPE), Co–Cr alloy] on the differentiation and functions of bone marrow stromal cells (BMSCs). Cells were isolated from femurs of BALB/c mice and cultured in complete osteoblast‐induction medium in presence of micron‐sized biomaterial particles at various doses. 3‐(4,5)‐Dimethylthiazol‐2‐yl)‐2,5‐diphenyl tetrazolium bromide assay and lactate dehydrogenase assay were performed for cell proliferation and cytotoxicity. Differentiation and function of osteoblasts were evaluated by alkaline phosphatase (ALP), osteocalcin, RANKL, OSX, and Runx2 expressions. Murine interleukin‐1 (IL‐1), IL‐6, and tumor necrosis factor‐α in culture media were determined by enzyme‐linked immunosorbent assay. Challenge with low doses of Ti, UHMWPE, or Co–Cr particles markedly promoted the bone marrow cell proliferation while high dose of Co–Cr significantly inhibited cell growth (p < 0.05). Cells challenged with low dose of PMMA or UHMWPE particles (0.63 mg/mL) exhibited strong ALP activity, whereas Ti and Co–Cr groups showed minimal effects (p < 0.05). UHMWPE and Ti particles also promoted higher expression of proinflammatory cytokines. Real‐time polymerase chain reaction data suggested that cells treated with low dose (0.5 mg/mL) particles resulted in distinctly diminished RANKL expression compared to those exposed to high concentrated (3 mg/mL) particles. In conclusion, various types of wear debris particles behaved differently in the differentiation, maturation, and functions of osteogenic cells; and the particulate debris‐interacted BMSCs may play an important role in the pathogenesis and process of the debris‐associated aseptic prosthetic loosening. © 2013 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 101A: 2817–2825, 2013.
Bibliography:istex:E515C0C6A69CB4FCA18FA7D7C82D1C82FF36E087
ark:/67375/WNG-F00M1J7F-C
National Institutes of Health - No. 5R03AR054929 (S-YY)
Orthopaedic Research Institute, Via Christi Health
ArticleID:JBMA34595
Dr. Paul H. Wooley is a Consultant to the Legal Representatives of Depuy, Inc. He receives no financial benefit for this service.
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ISSN:1549-3296
1552-4965
DOI:10.1002/jbm.a.34595