The role played by cell-substrate interactions in the pathogenesis of osteoclast-mediated peri-implant osteolysis
© Shen et al.; licensee BioMed Central Ltd. 2006
Received: 17 January 2006
Accepted: 14 March 2006
Published: 13 April 2006
Prosthetic wear debris-induced peri-implant osteolysis is a major cause of aseptic loosening after total joint replacement. In this condition, wear particles released from the implant components induce a granulomatous inflammatory reaction at the interface between implant and adjacent bone, leading to progressive bone resorption and loss of fixation. The present study was undertaken to characterize definitively the phenotype of osteoclast-like cells associated with regions of peri-implant focal bone resorption and to compare the phenotypic features of these cells with those of mononucleated and multinucleated cells associated with polyethylene wear particles. Peri-implant tissues were obtained from patients undergoing hip revision surgery for aseptic loosening after total joint replacement. Cells were examined for the expression of several markers associated with the osteoclast phenotype using immunohistochemistry, histochemistry, and/or in situ hybridization. CD68 protein, a marker expressed by multiple macrophage lineage cell types, was detected in mononucleated and multinucleated cells associated with polyethylene particles and the bone surface. Cathepsin K and tartrate-resistant acid phosphatase were expressed highly in both mononucleated and multinucleated cells associated with the bone surface. Levels of expression were much lower in cells associated with polyethylene particles. High levels of β3 integrin protein were detected in cells in contact with bone. Multinucleated cells associated with polyethylene particles exhibited faint positive staining. Calcitonin receptor mRNA expression was detected solely in multinucleated cells present in resorption lacunae on the bone surface and was absent in cells associated with polyethylene particles. Our findings provide further evidence that cells expressing the full repertoire of osteoclast phenotypic markers are involved in the pathogenesis of peri-implant osteolysis after total joint replacement. They also demonstrate that foreign body giant cells, although believed to be phenotypically and functionally distinct from osteoclasts, express many osteoclast-associated genes and gene products. However, the levels and patterns of expression of these genes in the two cell types differ. We speculate that, in addition to the role of cytokines and growth factors, the substrate with which these cells interact plays a critical role in their differential phenotypic and functional properties.
Inflammatory processes that target the skeleton are frequently accompanied by a localized disturbance in bone remodeling. The present study investigates a prototypical inflammatory disorder, namely peri-implant osteolysis after total joint replacement (TJR), in which localized bone resorption ultimately leads to loss of prosthetic fixation and implant loosening. In this condition, wear particles generated from orthopaedic implant components or from bone cement used for fixation gain access to the peri-implant bone interface, where they induce a granulomatous inflammatory reaction characterized by the presence of fibroblast-like cells, macrophages, and multinucleated foreign body giant cells. In localized areas where the inflammatory tissue is in contact with the bone surface there are focal regions containing mononucleated and multinucleated 'osteoclast-like' cells residing within resorption lacunae. These osteoclast-like cells have been implicated in the pathogenesis of the bone resorption associated with peri-implant osteolysis. Takagi and coworkers  demonstrated high-turnover peri-prosthetic bone remodeling and immature bone formation around loosened total hip replacement implants, indicating that the key role for the peri-implant osteoclast is in peri-implant bone resorption.
The macrophages, multinucleated foreign body giant cells, and osteoclasts that are present within the peri-implant tissues are derived from a common hematopoietic lineage, and a variety of phenotypic markers have been utilized to distinguish these cells from each other. Included among these are a variety of genes and gene products that impart to the osteoclast the unique capacity to recognize and bind to the bone surface in order to resorb a mineralized bone matrix. The attachment and activation of the osteoclast has been shown to involve several different integrins, including the vitronectin receptor αvβ3 [2, 3]. Expression of this integrin has served as a useful marker to identify osteoclasts and to distinguish them from their colony forming unit-macrophage (CFU-M) precursors that do not express the β3 gene . Additional gene products that are essential for creating an acidic environment for mineral dissolution and resorption of the organic matrix of bone are induced during osteoclast differentiation. Cathepsin K and tartrate-resistant acid phosphatase (TRAP) are among the enzymes that are expressed in these cells and contribute to the resorption of the extracellular matrix component of bone [5–7].
Although the expressions of these genes have served as useful markers to identify osteoclasts, several studies have demonstrated that their expression is not restricted to osteoclasts. For example, under certain conditions, TRAP activity and cathepsin K have been detected in cells that are not involved directly in bone resorption [8–10]. In our own studies involving analysis of synovial tissues from patients with rheumatoid arthritis  we observed that, in addition to cathepsin K and TRAP expression, osteoclast-like cells in resorption lacunae at the bone-pannus interface express the calcitonin receptor (CTR). In in vitro mouse and human osteoclast differentiation models, expression of the CTR occurs during the terminal stage of osteoclast differentiation, and activation coincides with the competence of the cell to resorb bone. The expression of this gene and gene product can thus be used to help discriminate mature osteoclasts from macrophages or macrophage polykaryons, and to identify osteoclasts that are actively involved in bone resorption.
In the present study we utilized immunohistochemical, histochemical and in situ hybridization techniques to analyze the phenotype of cells in human peri-implant tissues from patients with aseptic implant loosening after TJR. Special attention was focused on the differential phenotype of cells associated with polyethylene wear particles or the bone surface. Our results provide further evidence that cells expressing the full repertoire of osteoclast phenotypic markers are involved in the pathogenesis of peri-implant osteolysis after TJR. They also demonstrate that foreign body giant cells, although believed to be phenotypically and functionally distinct from osteoclasts, express many osteoclast-associated genes and gene products. However, the levels and pattern of expression of these genes in the two cell types differs. Osteoclasts and foreign body giant cells are derived from a common hematopoietic precursor, and we speculate that, in addition to the role of cytokines and growth factors, the substrate with which these cells interacts plays a critical role in their differential phenotypic and functional properties.
Materials and methods
Human tissue collection and preparation
Human peri-implant tissues associated with foreign body reactions to orthopedic implant wear debris were obtained from 12 patients. These patients had a clinical history of osteoarthritis and were undergoing revision surgery for aseptic loosening of prosthetic components after total hip replacement. The patients' ages ranged between 45 and 87 years; nine were female and three were male. Patients with a prior history of inflammatory arthritis were excluded from the analyses. The study protocol was approved by the New England Baptist Hospital and the Beth Israel Deaconess Medical Center Institutional Review Boards, and informed consent was obtained from all patients before surgery.
Specimens of soft tissue and bone were collected from regions of bone resorption during joint revision surgery. The specimens were fixed in freshly prepared 4% paraformadehyde, followed by demineralization with 14% EDTA in phosphate-buffered saline (PBS). The specimens were processed and embedded in paraffin and 5 μm sections were prepared for histological, histochemical, and immunohistochemical analyses.
Reagents for immunohistochemical detection and probes for in situhybridisation
Antibodies included a rabbit polyclonal antibody to human CD68 (sc-9139; Santa Cruz Biotechnology Inc., Santa Cruz, CA, USA), which identifies macrophages and osteoclasts, and a goat polyclonal antibody to human β3 integrin (sc-6627; Santa Cruz Biotechnology Inc., Santa Cruz, CA, USA). A rabbit polyclonal antibody to human cathepsin K was kindly provided by Dr D Bromme. The ABC avidin-biotin-peroxidase complex kits were purchased from Vector Laboratories (Burlingame, CA USA). RNA antisense probes for cathepsin K, TRAP, and CTR were prepared as previously reported [11,12] and sense probes were used as negative controls.
Histochemical staining for TRAP activity was done as previously reported . The sections were incubated with the reagents at 37°C for 10–20 minutes followed by counterstaining with hematoxylin.
For immunohistochemistry, sections were dewaxed and subjected to antigen retrieval in 10 mmol/l EDTA (pH 7.5) and microwaved at 93°C for 7 minutes. Immunohistochemical staining was performed as previously reported . Briefly, after rinsing with PBS the sections were pretreated with 3.0% hydrogen peroxide at room temperature for 20 minutes to inhibit endogenous peroxidase. Sections were then treated with blocking solution containing 1.5% (vol/vol) normal goat or rabbit serum (based on the animal secondary antibodies) and 10% fetal calf serum for 60 minutes at room temperature. Excess serum was gently blotted off and the sections were incubated with primary antibodies diluted in PBS containing 1.5% bovine serum albumin (CD68 1:100, β3 integrin 1:200 and cathepsin K 1:8000) at 4°C overnight or for 2 hours at room temperature. After thorough rinsing, the sections were incubated with an affinity-purified, biotinylated secondary antibody (1:200 in PBS), followed by incubation with avidin-biotin-peroxidase complex for 30 minutes each, at room temperature. After rinsing, the sections were developed with diaminobenzidine tetrahydrochloride substrate (Vector Laboratoriess, Burlingame, CA USA) and counterstained with hematoxylin, and then sealed with Permount (Fisher Scientific Company, Fair Lawn, NJ, USA). Sections were observed and photographed using a Nikon transmitted light microscope. Routine control experiments for checking specificity of the primary and secondary antibodies were performed by replacing the specific antibody with normal IgG or PBS.
For in situ hybridization, RNA sense and antisense probes were transcribed and labeled with 35S dATP (New Life Science, Boston, MA, USA) using an in vitro transcription kit, as previously described [11, 12]. The hybridization solution contained the following: 50% (vol/vol) de-ionized formamide; 10% (weight/vol) dextran sulphate; 1 × Denhardt's solution; 0.02% (weight/vol) of each of bovine serum albumin, Ficoll and polyvinylpyrrolidone, 4 × SSC (sodium chloride and sodium citrate), denatured salmon sperm DNA (0.5 μg/μl) and yeast tRNA (0.25 μg/μl); 1% (weight/vol) sodium N-lauroylsarcosinate; and 20,000 counts per minute (cpm) 35S-labeled oligonucleotide probe per microliter. Dithiothreitol was directly added at 0.1 mol/l to the hybridization solution before use.
The hybridization procedures used were similar to those used previously [11, 12]. Briefly, sections were dewaxed and post-fixed in 4% (weight/vol) freshly prepared paraformadehyde in PBS, acetylated with 0.25% (vol/vol) acetic anhydride in 0.1 mol/l triethanolamine buffer, and then dehydrated in increasing concentrations of ethanol. Each section was hybridized with 105 cpm labeled sense or antisense RNA probes in a humid chamber overnight at 52°C. After hybridization, the sections were washed in 2 × SSC at 50°C and then dehydrated in an ascending series of ethanol solutions containing 0.3 mol/l ammonium acetate. After dipping in Kodak photographic emulsion, the sections were stored with desiccant at 4°C for 12–20 weeks. The photoemulsion was developed and fixed, and sections were counterstained with hematoxylin and mounted in Kaiser's medium (glycerol/gelatin; Merck, Darmstadt, Germany). The slides were examined and photographed with both bright-field and dark-field illumination.
Aseptic loosening of prosthetic joint implants has emerged as the major long-term complication after TJR. The radiographic hallmark of prosthetic loosening is the presence of radiolucent zones at the interface between the bone and adjacent implant materials [15–18]. These zones of osteolysis develop as a consequence of an active biologic process involving the resorption of bone at the peri-implant sites. Insights into the mechanisms involved in this focal disorder of bone remodeling have been provided by histopathologic examination and biochemical analysis of the tissues obtained at revision surgery from patients who have developed aseptic loosening after TJR [17, 19–23]. Charnley , in his studies of the natural history of patients after total hip replacement, was the first to describe the presence of a 'macrophage foreign body reaction' associated with fragmented methylmethacrylate cement in peri-implant tissues from loosened prostheses. Subsequently, studies have shown that wear particles from orthopedic prosthetic devices of different composition, including polyethylene and metal, have the capacity to induce a foreign body granulomatous reaction [19, 20, 25–28].
Cells exhibiting phenotypic features of macrophages and macrophage polykaryons (so-called foreign body giant cells) are the principal cell types within the peri-implant granuloma [17, 20, 21, 23, 27, 28]. In the regions immediately adjacent to the implant surface the cells are frequently organized into a lining layer with histologic features of synovium . Analysis of the granuloma-bone interface has revealed highly variable cellular composition. In many regions the bone is lined by cells that exhibit a fibroblastic morphology. These cells fail to express the CD68 antigen and are not believed to be of hematopoietic origin. The association of the fibroblastic cells with the bone surface and the ex vivo demonstration that they can resorb a bone matrix have led some investigators to speculate that these cells represent a connective tissue subtype possessing a unique capacity to resorb bone . In addition to the bone-tissue interface populated by fibroblasts, Willert and coworkers  described regions of the bone surface that were lined by multinucleated cells with morphologic features of osteoclasts residing in resorption lacunae. Based on these observations, the conclusion was drawn that the osteolytic process was mediated principally via osteoclastic mechanisms.
Greenfield and coworkers  and other investigators [30–32] have suggested that increased recruitment of osteoclast precursors and their differentiation play a major role in wear particle induced osteolysis. To identify the source of the osteoclasts associated with the peri-implant osteolysis, Athanathou's group [14, 33, 34] and other investigators  have isolated cells from peri-implant granulomatous tissue from patients with aseptic loosening and showed that a subset of the mononuclear cells isolated from the tissue could be induced to form bone resorbing osteoclasts when cultured under appropriate conditions. These findings firmly establish the existence of osteoclast precursors within the granuloma of peri-implant tissue. It is presumed that this pool of cells gives rise to the osteoclasts that are associated with the bone surface and mediate the osteolytic process in vivo.
Cathepsin K and TRAP are among the enzymes that are expressed by osteoclasts. The importance of these two gene products in osteoclast functional activity is indicated by the resorptive defect in osteoclast-mediated bone resorption in mice in which either of these genes has been deleted [36, 37]. In humans, inactivating mutations in the cathepsin K gene are associated with an osteoclast resorbing defect manifest by pycnodysostosis . In the present study we detected cathepsin K and TRAP expression in mononuclear and multinuclear cells associated with polyethylene particles as well as the bone surface. These findings are consistent with the observations reported by Ren and coworkers , who found that polyethylene particles also induced cathepsin K and TRAP expression in an air pouch implantation model, and by Konttinen and colleagues , who found cathepsin K to be highly expressed in bone resorption around total hip replacement prosthesis. Of importance, in our studies we observed that the levels of expression of both cathepsin K and TRAP were much higher in the cells associated with the bone surface compared with the polyethylene particles. This was evident at the mRNA as well as the protein or functional level. We speculate that interaction with the bone substrate may play a critical role inducing the higher levels of expression of these two enzymes in cells associated with the bone surface, as discussed below.
Although expressions of the cathepsin K and TRAP genes have served as markers of the osteoclast phenotype, under certain conditions cathepsin K and TRAP activity have been detected in cells that are not involved directly in bone resorption [8–10, 40], indicating that their expression is not restricted to osteoclasts. For example, macrophages have been shown to express both of these enzymes . In the present study we observed that β3 integrin and CTR were preferentially expressed in cells associated with the bone surface. A number of studies have shown that neither the β3 integrin nor the CTR are expressed by osteoclast precursors. The expression of these genes increases during the late stages of osteoclast differentiation , after induction of the cathepsin K and TRAP genes. Importantly, the transcriptional activation of the β3 integrin and CTR genes coincides with the transition of the osteoclast to an actively resorbing cell . Thus, based on these in vitro studies, the levels of expression of these genes can be used to discriminate osteoclasts from macrophages or macrophage polykaryons, and to identify osteoclasts that are actively involved in bone resorption. Our results suggest that expression of the CTR may be a more definitive marker of terminal osteoclast differentiation than the β3 integrin because it was solely confined to the bone matrix whereas β3 was very weakly detected on some multinucleated cells associated with wear particles. Because osteoclast cells express relatively low levels of CTR mRNA, it is also possible, as with the β3 integrin, that CTR could be expressed in the cells associated with the polyethylene particles but the levels were below the limits of detection.
Relatively few studies have rigorously compared the functional and phenotypic features of the multinucleated foreign body giant cells associated with wear particles and the multinucleated osteoclast-like cells detected in resorption lacunae at sites of peri-implant osteolysis. Willert and coworkers  commented on the absence of wear particles in osteoclast-like cells in resorption lacunae and speculated that they were phenotypically distinct from the polykaryons associated with the implant wear particles. More recently, Athanasou and coworkers [14, 43] cultured mononuclear cells isolated from the peri-implant tissues retrieved from patients with granulomatous reactions to implant materials. They showed that both monocyte/macrophages and cells expressing phenotypic features of foreign body giant cells could produce 'resorption pits' on bone slices. The level of resorption produced by these cells, however, was considerably less than that observed with authentic osteoclasts. This suggests that the cells associated with wear particles, despite being multinuclear, are functionally distinct from osteoclasts. These observations support the work of others who have found that macrophages or macrophage polykaryons have a limited capacity to resorb a mineralized bone matrix [26, 27, 44].
Further evidence indicating the differential phenotype of foreign body giant cells and osteoclast cells is provided by our previous studies [45, 46] in which we implanted particles of polyethylene or polymethylmethacrylate into soft tissues of rats and analyzed the phenotypic features of the elicited cells. We observed that the particulate polymeric materials failed to induce cells with the full phenotypic and functional properties of osteoclasts. In these studies we also implanted mineralized bone particles of size comparable to that of the polyethylene and polymethylmethacrylate particles. The bone, similar to the polymeric materials, induced a granulomatous inflammatory reaction. However, in contrast to the polymeric material, the bone particles induced multiunucleated cells expressing TRAP activity as well as CTR. Most importantly, these cells were able to resorb the bone matrix, thus establishing their authenticity as osteoclast cells. These observations, and the findings of the present study using human peri-implant tissues, indicate that binding of cells to polyethylene wear particles or bone results in differential phenotypic expression. Based on these findings we speculate that binding and interaction of cells with the different substrates play important roles in regulating their differential phenotypic and functional activity.
In the present study we noted the presence of abundant CD68 positive mononucleated and multinucleated cells associated with the polyethylene particles. Cells within resorption lacunae at the bone surface also expressed this antigen. Other studies have shown that osteoclasts, as well as CFU-M lineage macrophages, express CD68, and we speculate that the CD68-positive mononuclear cells within the granuloma represent the precursors for the osteoclast-like cells involved in the resorptive process at the bone surface. This conclusion is supported by recent studies conducted by Sabokbar and coworkers , who demonstrated that macrophages isolated directly from peri-implant tissues surrounding loosened implants exhibited limited capacity to resorb bone. However, under appropriate culture conditions they could be induced ex vivo to differentiate into multinucleated cells with the full functional and cytochemical characteristics of osteoclasts. These findings received support from a study conducted by Haynes and coworkers .
Our results provide further evidence implicating osteoclasts in the pathogenesis of the peri-implant osteolysis associated with prosthetic implant wear debris. The findings of TRAP and cathepsin K expression in macrophages and foreign body giant cells associated with wear particles expression confirms our previous observations, as well as the findings of others, that these two enzymes are not definitive markers of the osteoclast phenotype [8–10, 41]. β3 Integrin and CTR are associated with later stage cells of osteoclast differentiation, and their levels of expression were much high in cells in contact with bone as opposed to wear particles. The expression of the CTR appears to discriminate osteoclasts from foreign body giant cells and other CFU-M lineage cells because it is expressed solely by cells on the bone. The findings supporting a role for osteoclasts in the pathogenesis of peri-implant osteolysis have important clinical implications and suggest that targeting osteoclasts, as well as the pathways that regulate osteoclast differentiation and activation, represents a rational therapeutic approach to preventing this major clinical complication after TJR.
colony forming units-macrophage
calcitonin receptor; counts per minute (cpm)
total joint replacement
tartrate resistant acid phosphatase.
We thank Dr Bromme for providing anti-cathepsin K antibody and Alfie Tsay for performing in situ hybridization. This work was supported in part by National Institutes of Health Grants NIAMS R01 AR45472 (to SRG) and NIAMS R01 AR47229 (to KPM). TC holds a National Health and Medical Research Council (Aust) CJ Martin Fellowship (ID 200078).
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