Micrometer-Sized Titanium Particles Induce Aseptic Loosening in Rabbit Knee

Wear debris induced aseptic loosening is the leading cause of total knee arthroplasty (TKA) failure. The complex mechanism of aseptic loosening has been a major issue for introducing effective prevention and treatment methods, so a simplified yet efficient rabbit model was established to address this concern with the use of micrometer-sized titanium particles. 20 New Zealand white rabbits were selected and divided into two groups (control = 10, study = 10). A TKA surgery was then performed for each of them, with implantation of a titanium rod prosthesis which was coated evenly with micrometer-sized titanium in the study group and nothing in the control group, into right femoral medullary cavity. After 12 weeks, all the animals were euthanized and X-ray analyses, H&E staining, Goldner Masson trichrome staining, Von Kossa staining, PCR, and Western blotting of some specific mRNAs and proteins in the interface membrane tissues around the prosthesis were carried out. The implantation of a titanium rod prosthesis coated with 20 μm titanium particles into the femoral medullary cavity of rabbits caused continuous titanium particle stimulation around the prosthesis, effectively inducing osteolysis and aseptic loosening. Titanium particle-induced macrophages produce multiple inflammatory factors able to activate osteoclast differentiation through the OPG/RANKL/RANK signaling pathway, resulting in osteolysis while suppressing the function of osteoblasts and reducing bone ingrowth around the prosthesis. This model simulated the implantation and loosening process of an artificial prosthesis, which is an ideal etiological model to study the aseptic prosthetic loosening.

[1]  A. Pearle,et al.  Annual revision rates of partial versus total knee arthroplasty: A comparative meta-analysis. , 2017, The Knee.

[2]  A. Fottner,et al.  Factors regulating bone remodeling processes in aseptic implant loosening , 2017, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.

[3]  M. Lamghari,et al.  Immune response and innervation signatures in aseptic hip implant loosening , 2016, Journal of Translational Medicine.

[4]  K. Hayashi,et al.  Risk factors for loosening of cementless threaded femoral implants in canine total hip arthroplasty , 2014, Veterinary and Comparative Orthopaedics and Traumatology.

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

[6]  Ziqing Li,et al.  Wear particles promote endotoxin tolerance in macrophages by inducing interleukin-1 receptor-associated kinase-M expression. , 2013, Journal of biomedical materials research. Part A.

[7]  M. Pagnano,et al.  Aseptic Tibial Debonding as a Cause of Early Failure in a Modern Total Knee Arthroplasty Design , 2013, Clinical orthopaedics and related research.

[8]  Jie Xu,et al.  In vitro comparison of the biological activity of alumina ceramic and titanium particles associated with aseptic loosening , 2012, Biomedical materials.

[9]  A. Odgaard,et al.  Existing data sources for clinical epidemiology: The Danish Knee Arthroplasty Register , 2012, Clinical epidemiology.

[10]  V. Denaro,et al.  Genetic susceptibility to aseptic loosening following total hip arthroplasty: a systematic review. , 2012, British medical bulletin.

[11]  M. Allen,et al.  The dog as a preclinical model to evaluate interface morphology and micro-motion in cemented total knee replacement , 2011, Veterinary and Comparative Orthopaedics and Traumatology.

[12]  W. Marsden I and J , 2012 .

[13]  Kerong Dai,et al.  Pathways of macrophage apoptosis within the interface membrane in aseptic loosening of prostheses. , 2011, Biomaterials.

[14]  B. Masri,et al.  Quality of life outcomes in revision versus primary total knee arthroplasty. , 2011, The Journal of arthroplasty.

[15]  S. Niida,et al.  Wear Debris Stimulates Bone-Resorbing Factor Expression in the Fibroblasts and Osteoblasts , 2011, Hip international : the journal of clinical and experimental research on hip pathology and therapy.

[16]  U. Quint,et al.  Senescence in cells in aseptic loosening after total hip replacement. , 2011, Acta biomaterialia.

[17]  S. Goodman,et al.  Continuous Infusion of UHMWPE Particles Induces Increased Bone Macrophages and Osteolysis , 2011, Clinical orthopaedics and related research.

[18]  Tang Tingting,et al.  Enhancement of osteoblast differentiation that is inhibited by titanium particles through inactivation of NFATc1 by VIVIT peptide. , 2010, Journal of biomedical materials research. Part A.

[19]  J. Tong,et al.  Bone-cement interfacial behaviour under mixed mode loading conditions. , 2010, Journal of the mechanical behavior of biomedical materials.

[20]  G. Saxler,,et al.  Polyethylene Particle–Induced Bone Resorption in α‐Calcitonin Gene–Related Peptide–Deficient Mice , 2007, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[21]  V. Goldberg,et al.  Comparison of the roles of IL-1, IL-6, and TNFalpha in cell culture and murine models of aseptic loosening. , 2007, Bone.

[22]  Richard E. Costello,et al.  Murine model of prosthesis failure for the long‐term study of aseptic loosening , 2007, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.

[23]  C. Rorabeck,et al.  Wear and osteolysis around total knee arthroplasty. , 2007, The Journal of the American Academy of Orthopaedic Surgeons.

[24]  Peter Thomsen,et al.  Aseptic loosening, not only a question of wear: A review of different theories , 2006, Acta orthopaedica.

[25]  L. White,et al.  Effect of Zoledronate on Bone Quality in the Treatment of Aseptic Loosening of Hip Arthroplasty in the Dog , 2005, Calcified Tissue International.

[26]  R. Marti,et al.  Effects of mechanical compression of a fibrous tissue interface on bone with or without high-density polyethylene particles in a rabbit model of prosthetic loosening. , 2005, The Journal of bone and joint surgery. American volume.

[27]  S. Avnet,et al.  Molecular basis of osteoclastogenesis induced by osteoblasts exposed to wear particles. , 2005, Biomaterials.

[28]  Ann L. Johnson,et al.  An animal model for interface tissue formation in cemented hip replacements. , 2004, Veterinary surgery : VS.

[29]  L. Meinel,et al.  An experimental animal model of aseptic loosening of hip prostheses in sheep to study early biochemical changes at the interface membrane , 2004, BMC musculoskeletal disorders.

[30]  E. Schwarz,et al.  Aseptic loosening , 2004, Gene Therapy.

[31]  C. R. Howlett,et al.  Prosthetic particles modify the expression of bone-related proteins by human osteoblastic cells in vitro. , 2003, Biomaterials.

[32]  J. Corbeil,et al.  Gene expression analysis of osteoblastic cells contacted by orthopedic implant particles. , 2002, Journal of biomedical materials research.

[33]  R. Gay,et al.  Development and characteristics of a synovial-like interface membrane around cemented tibial hemiarthroplasties in a novel rat model of aseptic prosthesis loosening. , 2001, Arthritis and rheumatism.

[34]  P. Aspenberg,et al.  Pressure‐induced periprosthetic osteolysis: A rat model , 2000, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.

[35]  D P Pioletti,et al.  The cytotoxic effect of titanium particles phagocytosed by osteoblasts. , 1999, Journal of biomedical materials research.

[36]  J. Hart,et al.  Joint replacement surgery , 2004, The New England journal of medicine.

[37]  W. Remagen,et al.  [On the problem of osteolysis]. , 1967, Frankfurter Zeitschrift fur Pathologie.