Direct influence of titanium and zirconia particles on the morphology and functionality of mature human osteoclasts.

Within the last ten years of biomedical implants, the focus is increasingly on bioceramics, specifically on zirconia (ZrO2 ). Hence, we analyzed the impact of ZrO2 particles in comparison to titanium particles on mature human osteoclasts (OCs) as little is known about the direct effect of wear particles on mature OCs and their role in the osteolytic process during aseptic endoprosthesis loosening. Changes in cell morphology and functionality of OCs incubated with particles in different concentrations were investigated in vitro. OCs tend to be enlarged after three days of cultivation with both types of particles, especially with high concentrations of ZrO2 , suggesting increased cell fusion. Further, we identified significantly increased expression of OC specific and bone matrix related genes: VNR, RANK, TRAP, and CTSK pointing on a direct stimulatory particle effect on the functionality of mature OCs. In completion, we quantified the bone resorption activity of particle treated mature OCs but could not detect a significant difference in bone resorption compared to OCs cultivated without particles. However, we could identify significantly higher gene expression of MMP-1 in particle treated OCs compared to untreated control OCs after three days of incubation. We also detected an impaired production of the tissue inhibitor of metalloproteinase, especially for OCs treated with high ZrO2 concentrations. In conclusion, our in vitro data show that abrasion particles could have a direct influence on mature OCs and therefore could promote increased OC-mediated bone resorption during aseptic loosening of total joint replacements. © 2017 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 105A: 2608-2615, 2017.

[1]  J. Parvizi,et al.  Biological response to prosthetic debris. , 2015, World journal of orthopedics.

[2]  M. Swain,et al.  Adhesion determination of dental porcelain to zirconia using the Schwickerath test: strength vs. fracture energy approach. , 2014, Acta biomaterialia.

[3]  Jukka Pekka Matinlinna,et al.  Ceramic dental biomaterials and CAD/CAM technology: state of the art. , 2014, Journal of prosthodontic research.

[4]  B. Yu,et al.  BMP-2 and titanium particles synergistically activate osteoclast formation , 2014, Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas.

[5]  P. Wooley,et al.  Effects of Ti, PMMA, UHMWPE, and Co-Cr wear particles on differentiation and functions of bone marrow stromal cells. , 2013, Journal of biomedical materials research. Part A.

[6]  M. Wimmer,et al.  Osteolysis around total knee arthroplasty: a review of pathogenetic mechanisms. , 2013, Acta biomaterialia.

[7]  B. Devitt,et al.  The role of osteoblasts in peri-prosthetic osteolysis. , 2013, The bone & joint journal.

[8]  C. Schulze,et al.  Cell viability, collagen synthesis and cytokine expression in human osteoblasts following incubation with generated wear particles using different bone cements. , 2013, International journal of molecular medicine.

[9]  Haiyang Yu,et al.  Suture compression induced bone resorption with intensified MMP-1 and 13 expressions. , 2012, Bone.

[10]  R. Bader,et al.  The potential role of human osteoblasts for periprosthetic osteolysis following exposure to wear particles. , 2011, International journal of molecular medicine.

[11]  S. Knight,et al.  Total Hip Arthroplasty - over 100 years of operative history , 2011, Orthopedic reviews.

[12]  K. Mihara,et al.  Molecular mechanisms and physiologic functions of mitochondrial dynamics. , 2011, Journal of biochemistry.

[13]  M. Oursler Recent advances in understanding the mechanisms of osteoclast precursor fusion , 2010, Journal of cellular biochemistry.

[14]  V. Geoffroy,et al.  Bone loss induced by Runx2 Over‐expression in mice is blunted by osteoblastic over‐expression of TIMP‐1 , 2010, Journal of cellular physiology.

[15]  Xu Yang,et al.  Polymethylmethacrylate particles stimulate bone resorption of mature osteoclasts in vitro , 2008, Acta orthopaedica.

[16]  J. Triffitt,et al.  A review on macrophage responses to biomaterials , 2006, Biomedical Materials.

[17]  John Fisher,et al.  The role of macrophages in osteolysis of total joint replacement. , 2005, Biomaterials.

[18]  V. Geoffroy,et al.  In Vivo Inhibition of Osteoblastic Metalloproteinases Leads to Increased Trabecular Bone Mass , 2004, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[19]  V. Goldberg,et al.  The role of osteoclast differentiation in aseptic loosening , 2002, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.

[20]  T. Glant,et al.  Osteolysis: basic science. , 2001, Clinical orthopaedics and related research.

[21]  V. Goldberg,et al.  Titanium Particles Stimulate Bone Resorption by Inducing Differentiation of Murine Osteoclasts , 2001, The Journal of bone and joint surgery. American volume.

[22]  D. Schurman,et al.  In vitro reaction to orthopaedic biomaterials by macrophages and lymphocytes isolated from patients undergoing revision surgery. , 2001, Biomaterials.

[23]  D. Howie,et al.  The effect of particle phagocytosis and metallic wear particles on osteoclast formation and bone resorption in vitro. , 2000, The Journal of arthroplasty.

[24]  J. Compston,et al.  Tissue inhibitor of matrix metalloproteinase-1 (TIMP-1) distribution in normal and pathological human bone. , 1999, Bone.

[25]  R. Huber,et al.  Mechanism of inhibition of the human matrix metalloproteinase stromelysin-1 by TIMP-1 , 1997, Nature.

[26]  J. Compston,et al.  Distribution of matrix metalloproteinases and their inhibitor, TIMP‐1, in developing human osteophytic bone , 1997, Journal of anatomy.

[27]  S. Goodman,et al.  The basic science of periprosthetic osteolysis. , 2013, Instructional course lectures.

[28]  J A Wimhurst,et al.  Current concepts in osteolysis. , 2012, The Journal of bone and joint surgery. British volume.