Nitric Oxide and Prostaglandin E2 Production in Response to Ultra-High Molecular Weight Polyethylene Particles Depends on Osteoblast Maturation State

Background: Recent studies have shown that osteoblast-like cells respond directly to ultra-high molecular weight polyethylene particles in culture, suggesting that they may be involved in aseptic loosening of endoprostheses. We tested the hypothesis that the state of cell maturation plays a role in the response of osteogenic cells to ultra-high molecular weight polyethylene particles.Methods: MG63 cells (immature osteoblast-like cells), OCT-1 cells (mature secretory osteoblast-like cells), and MLO-Y4 cells (osteocyte-like cells) were treated for twenty-four hours with commercial ultra-high molecular weight polyethylene particles with an average diameter of 1 mm. The effect of particle treatment on cell proliferation was assessed by measuring the number of cells, whereas the effects on differentiation and local factor production were assessed by measuring the production of osteocalcin, prostaglandin E2, and nitric oxide. The effect of particles on apoptosis was also evaluated.Results: The addition of ultra-high molecular weight polyethylene particles increased the number of MG63 cells, did not affect the number of OCT-1 cells, and led to a decrease in the number of MLO-Y4 cells. The observed changes in cell number were not due to programmed cell death, as no more than 3% of the cells in cultures treated with the highest concentration of particles were undergoing apoptosis. Osteocalcin production was not affected by the addition of particles. Prostaglandin E2 production was increased in all three types of cultures, but the effect was greatest in OCT-1 cell cultures, as was the absolute amount of prostaglandin E2 produced. Nitric oxide production was unaffected in MG63 cell cultures, but it was stimulated in OCT-1 and MLO-Y4 cell cultures.Conclusions: The results of the present study support the hypothesis that osteoblast cell maturation state plays an important role in the response to ultra-high molecular weight polyethylene particles and that the terminally differentiated osteocyte may be involved in the bone response to wear debris in vivo.Clinical Relevance: Because maturation state in the osteoblast lineage is an important factor in the cellular response to wear debris and the osteocyte is surprisingly sensitive to ultra-high molecular weight polyethylene particles, and because these cells have been shown to be in direct contact with the bone-implant interface via canaliculi, their role in aseptic loosening needs to be considered.

[1]  C. Lohmann,et al.  Effect of polymer molecular weight and addition of calcium stearate on response of MG63 osteoblast‐like cells to UHMWPE particles , 2001, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.

[2]  L. Bonewald,et al.  Maturation State Determines the Response of Osteogenic Cells to Surface Roughness and 1,25‐Dihydroxyvitamin D3 , 2000, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[3]  A. U. Daniels,et al.  Macrophage cytokine response to particles and lipopolysaccharide in vitro. , 2000, Journal of biomedical materials research.

[4]  C. Lohmann,et al.  Human osteoblast-like cells phagocytose metal particles and express the macrophage marker CD68 in vitro. , 2000, The Journal of bone and joint surgery. British volume.

[5]  B. Boyan,et al.  Phagocytosis of wear debris by osteoblasts affects differentiation and local factor production in a manner dependent on particle composition. , 2000, Biomaterials.

[6]  K. Merritt,et al.  Decontaminating particles exposed to bacterial endotoxin (LPS). , 1999, Journal of biomedical materials research.

[7]  C. Hamanishi,et al.  Pertussis toxin‐sensitive G proteins as mediators of stretch‐induced decrease in nitric‐oxide release of osteoblast‐like cells , 1999, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.

[8]  Lynda F. Bonewald,et al.  Identification and Characterization of a Novel Protein, Periostin, with Restricted Expression to Periosteum and Periodontal Ligament and Increased Expression by Transforming Growth Factor β , 1999 .

[9]  C. M. Agrawal,et al.  The effect of ultra-high molecular weight polyethylene wear debris on MG63 osteosarcoma cells in vitro. , 1999, The Journal of bone and joint surgery. American volume.

[10]  C. Lohmann,et al.  Ultrahigh molecular weight polyethylene particles have direct effects on proliferation, differentiation, and local factor production of MG63 osteoblast‐like cells , 1999, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.

[11]  S. Santavirta,et al.  Nitric oxide in the local host reaction to total hip replacement. , 1998, Clinical orthopaedics and related research.

[12]  P. Huie,et al.  Inducible nitric oxide synthase messenger RNA levels in hip periprosthetic tissue: a preliminary study. , 1998, Journal of biomedical materials research.

[13]  T. Young,et al.  Ultrastructural analyses of the attachment (bonding) zone between bone and implanted biomaterials. , 1998, Journal of biomedical materials research.

[14]  L. Bonewald,et al.  Establishment of an Osteocyte‐like Cell Line, MLO‐Y4 , 1997, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[15]  D. Howie,et al.  Regulation of bone cells by particle-activated mononuclear phagocytes. , 1997, The Journal of bone and joint surgery. British volume.

[16]  J. Compston,et al.  Principles of Bone Biology , 1997 .

[17]  P. Millett,et al.  The effects of particulate cobalt, chromium and cobalt-chromium alloy on human osteoblast-like cells in vitro. , 1997, The Journal of bone and joint surgery. British volume.

[18]  Simon C Watkins,et al.  Short Communication Identification of Inducible Nitric Oxide Synthase in Human Macrophages Surrounding Loosened Hip Prostheses , 2022 .

[19]  T. Glant,et al.  Suppression of Osteoblast Function by Titanium Particles*† , 1997, The Journal of bone and joint surgery. American volume.

[20]  L. Lidgren,et al.  Polyethylene and titanium alloy particles reduce bone formation. Dose-dependence in bone harvest chamber experiments in rabbits. , 1996, Acta orthopaedica Scandinavica.

[21]  J. B. Gonzales,et al.  Inflammatory Response to Implant Particulates in a Macrophage/Osteoblast Coculture Model , 1996, Calcified Tissue International.

[22]  B D Boyan,et al.  Surface roughness modulates the local production of growth factors and cytokines by osteoblast-like MG-63 cells. , 1996, Journal of biomedical materials research.

[23]  J. Klein-Nulend,et al.  Prostaglandin mediated modulation of transforming growth factor‐β metabolism in primary mouse osteoblastic cells in vitro , 1996, Journal of cellular physiology.

[24]  J. Y. Martin,et al.  Effect of titanium surface roughness on chondrocyte proliferation, matrix production, and differentiation depends on the state of cell maturation. , 1996, Journal of biomedical materials research.

[25]  P. Nijweide,et al.  Pulsating fluid flow increases nitric oxide (NO) synthesis by osteocytes but not periosteal fibroblasts--correlation with prostaglandin upregulation. , 1995, Biochemical and biophysical research communications.

[26]  J. Polak,et al.  Cytokine-stimulated expression of inducible nitric oxide synthase by mouse, rat, and human osteoblast-like cells and its functional role in osteoblast metabolic activity. , 1995, Endocrinology.

[27]  W. Maloney,et al.  Isolation and characterization of wear particles generated in patients who have had failure of a hip arthroplasty without cement. , 1995, The Journal of bone and joint surgery. American volume.

[28]  Y. Pommier,et al.  The role of cell cycle regulation and apoptosis triggering in determining the sensitivity of leukemic cells to topoisomerase I and II inhibitors. , 1995, Leukemia.

[29]  A Sarmiento,et al.  The origin of submicron polyethylene wear debris in total hip arthroplasty. , 1995, Clinical orthopaedics and related research.

[30]  J. Riancho,et al.  Mechanisms controlling nitric oxide synthesis in osteoblasts , 1995, Molecular and Cellular Endocrinology.

[31]  Y. Saegusa,et al.  Cultured osteoblast synthesize nitric oxide in response to cytokines and lipopolysaccharide. , 1994, The Kobe journal of medical sciences.

[32]  Y. Gazitt,et al.  Fluctuations and ultrastructural localization of oncoproteins and cell cycle regulatory proteins during growth and apoptosis of synchronized AGF cells. , 1994, Cancer research.

[33]  D. Howie,et al.  The differences in toxicity and release of bone-resorbing mediators induced by titanium and cobalt-chromium-alloy wear particles. , 1993, The Journal of bone and joint surgery. American volume.

[34]  P. Stashenko,et al.  Proinflammatory cytokines tumor necrosis factor-alpha and IL-6, but not IL-1, down-regulate the osteocalcin gene promoter. , 1992, Journal of immunology.

[35]  H. Bertram,et al.  Osteolysis in alloarthroplasty of the hip. The role of ultra-high molecular weight polyethylene wear particles. , 1990, Clinical orthopaedics and related research.

[36]  L. Bonewald,et al.  Localization of 1,25-(OH)2D3-responsive alkaline phosphatase in osteoblast-like cells (ROS 17/2.8, MG 63, and MC 3T3) and growth cartilage cells in culture. , 1989, The Journal of biological chemistry.

[37]  P. K. Smith,et al.  Measurement of protein using bicinchoninic acid. , 1985, Analytical biochemistry.

[38]  R. Franceschi,et al.  1α, 25‐Dihydroxyvitamin D3 specific regulation of growth, morphology, and fibronectin in a human osteosarcoma cell line , 1985 .

[39]  R. Baron,et al.  PGE2 stimulates both resorption and formation of bone in vitro: Differential responses of the periosteum and the endosteum in fetal rat long bone cultures , 1985, The Anatomical record.

[40]  常男 高橋,et al.  [Collagen phagocytosis by osteoblast-like cells of mouse calvaria in vitro: an electron microscopic study]. , 1984 .

[41]  M. Semlitsch,et al.  Reaction of bone to methacrylate after hip arthroplasty: a long-term gross, light microscopic, and scanning electron microscopic study. , 1974, The Journal of bone and joint surgery. American volume.

[42]  D. Klein,et al.  Prostaglandins: stimulation of bone resorption in tissue culture. , 1970, Endocrinology.

[43]  K. Horiuchi,et al.  Identification and characterization of a novel protein, periostin, with restricted expression to periosteum and periodontal ligament and increased expression by transforming growth factor beta. , 1999, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[44]  L. Bonewald Establishment and characterization of an osteocyte-like cell line, MLO-Y4 , 1999, Journal of Bone and Mineral Metabolism.

[45]  B. Boyan,et al.  Titanium surface roughness alters responsiveness of MG63 osteoblast-like cells to 1 alpha,25-(OH)2D3. , 1998, Journal of biomedical materials research.

[46]  B. Boyan,et al.  Titanium surface roughness alters responsiveness of MG63 osteoblast‐like cells to 1α,25‐(OH)2D3 , 1998 .

[47]  L. Bonewald,et al.  Osteoblastic cell lines derived from a transgenic mouse containing the osteocalcin promoter driving SV40 T-antigen , 1995 .

[48]  P. Campbell,et al.  Isolation of predominantly submicron-sized UHMWPE wear particles from periprosthetic tissues. , 1995, Journal of biomedical materials research.

[49]  J O Galante,et al.  Composition and morphology of wear debris in failed uncemented total hip replacement. , 1994, The Journal of bone and joint surgery. British volume.

[50]  M. Ritter,et al.  Radiolucency at the bone-cement interface in total knee replacement. The effects of bone-surface preparation and cement technique. , 1994, The Journal of bone and joint surgery. American volume.

[51]  L. Bonewald,et al.  Differential regulation of prostaglandin E2 synthesis and phospholipase A2 activity by 1,25-(OH)2D3 in three osteoblast-like cell lines (MC-3T3-E1, ROS 17/2.8, and MG-63). , 1992, Bone.

[52]  R. Franceschi,et al.  1 alpha, 25-dihydroxyvitamin D3 specific regulation of growth, morphology, and fibronectin in a human osteosarcoma cell line. , 1985, Journal of cellular physiology.

[53]  R. Dziak Prostaglandins as Mediators of Bone Cell Metabolism , 1985 .

[54]  M. Kumegawa,et al.  [Collagen phagocytosis by osteoblast-like cells of mouse calvaria in vitro: an electron microscopic study]. , 1984, Nihon Shishubyo Gakkai kaishi.