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The Effect of Ultra-High Molecular Weight Polyethylene Wear Debris on MG63 Osteosarcoma Cells in Vitro

BackgroundFocal osteolysis due to ultra-high molecular weight polyethylene wear debris involves effects on both bone resorption and bone formation. MethodsThe response of MG63 osteoblast-like osteosarcoma cells to ultra-high molecular weight polyethylene wear debris isolated by enzymatic digestion o...

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Published in:Journal of bone and joint surgery. American volume 1999-04, Vol.81 (4), p.452-61
Main Authors: DEAN, D D, SCHWARTZ, Z, LIU, Y, BLANCHARD, C R, AGRAWAL, C M, MABREY, J D, SYLVIA, V L, LOHMANN, C H, BOYAN, B D
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cited_by cdi_FETCH-LOGICAL-c5092-570cf322511468d0059d2d38f02fe1f8b35fe6538566c4cfaa0df15b163450cd3
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container_title Journal of bone and joint surgery. American volume
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creator DEAN, D D
SCHWARTZ, Z
LIU, Y
BLANCHARD, C R
AGRAWAL, C M
MABREY, J D
SYLVIA, V L
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BOYAN, B D
description BackgroundFocal osteolysis due to ultra-high molecular weight polyethylene wear debris involves effects on both bone resorption and bone formation. MethodsThe response of MG63 osteoblast-like osteosarcoma cells to ultra-high molecular weight polyethylene wear debris isolated by enzymatic digestion of granulomatous tissue obtained from the sites of failed total hip arthroplasties was examined. Scanning electron microscopy, particle-size analysis, and Fourier transform infrared spectroscopy were used to characterize the number, morphology, size distribution, and chemical composition of the particles. Cell response was assessed by adding particles at varying dilutions to confluent cultures and measuring changes in cell proliferation (number of cells and [H]-thymidine incorporation), osteoblast function (alkaline-phosphatase-specific activity and osteocalcin production), matrix production (collagen production and proteoglycan sulfation), and local cytokine production (prostaglandin-E2 production). ResultsThe mean size of the particles was 0.60 micrometer, and 95 percent of the particles had a size of less than 1.5 micrometers. The number of particles per gram of tissue ranged from 1.39 to 3.38 x 10. Three of the four batches of particles were endotoxin-free. Exposure of the cells to particles of wear debris significantly increased the number of cells (p < 0.05) and the [H]-thymidine incorporation (p < 0.05) in a dose-dependent manner. In contrast, the addition of particles decreased alkaline-phosphatase-specific activity and osteocalcin production. Collagen production and proteoglycan sulfation were also decreased, while prostaglandin-E2 synthesis was increased by the addition of particles. ConclusionsUltra-high molecular weight polyethylene particles isolated from human tissue stimulated osteoblast proliferation and prostaglandin-E2 production and inhibited cell differentiation and matrix production. These results indicate that particles of wear debris inhibit cell functions associated with bone formation and that osteoblasts may produce factors in response to wear debris that influence neighboring cells, such as osteoclasts and macrophages. Clinical RelevanceParticles of wear debris, especially ultra-high molecular weight polyethylene, have been implicated in the loosening of implants and the development of osteolysis. The present study shows that particles of ultra-high molecular weight polyethylene isolated from human tissue inhibit osteoblast functions as
doi_str_mv 10.2106/00004623-199904000-00002
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MethodsThe response of MG63 osteoblast-like osteosarcoma cells to ultra-high molecular weight polyethylene wear debris isolated by enzymatic digestion of granulomatous tissue obtained from the sites of failed total hip arthroplasties was examined. Scanning electron microscopy, particle-size analysis, and Fourier transform infrared spectroscopy were used to characterize the number, morphology, size distribution, and chemical composition of the particles. Cell response was assessed by adding particles at varying dilutions to confluent cultures and measuring changes in cell proliferation (number of cells and [H]-thymidine incorporation), osteoblast function (alkaline-phosphatase-specific activity and osteocalcin production), matrix production (collagen production and proteoglycan sulfation), and local cytokine production (prostaglandin-E2 production). ResultsThe mean size of the particles was 0.60 micrometer, and 95 percent of the particles had a size of less than 1.5 micrometers. The number of particles per gram of tissue ranged from 1.39 to 3.38 x 10. Three of the four batches of particles were endotoxin-free. Exposure of the cells to particles of wear debris significantly increased the number of cells (p &lt; 0.05) and the [H]-thymidine incorporation (p &lt; 0.05) in a dose-dependent manner. In contrast, the addition of particles decreased alkaline-phosphatase-specific activity and osteocalcin production. Collagen production and proteoglycan sulfation were also decreased, while prostaglandin-E2 synthesis was increased by the addition of particles. ConclusionsUltra-high molecular weight polyethylene particles isolated from human tissue stimulated osteoblast proliferation and prostaglandin-E2 production and inhibited cell differentiation and matrix production. These results indicate that particles of wear debris inhibit cell functions associated with bone formation and that osteoblasts may produce factors in response to wear debris that influence neighboring cells, such as osteoclasts and macrophages. Clinical RelevanceParticles of wear debris, especially ultra-high molecular weight polyethylene, have been implicated in the loosening of implants and the development of osteolysis. The present study shows that particles of ultra-high molecular weight polyethylene isolated from human tissue inhibit osteoblast functions associated with bone formation. In addition, particles of wear debris induced osteoblasts to secrete factors capable of influencing neighboring cells, such as osteoclasts and macrophages. These results suggest that osteoblasts may play a role in the cascade of events leading to granuloma formation, osteolysis, and failure of orthopaedic implants.</description><edition>American volume</edition><identifier>ISSN: 0021-9355</identifier><identifier>EISSN: 1535-1386</identifier><identifier>DOI: 10.2106/00004623-199904000-00002</identifier><identifier>PMID: 10225790</identifier><identifier>CODEN: JBJSA3</identifier><language>eng</language><publisher>Boston, MA: Copyright by The Journal of Bone and Joint Surgery, Incorporated</publisher><subject>Adult ; Alkaline Phosphatase - metabolism ; Biological and medical sciences ; Cell Division ; Collagen - biosynthesis ; Culture Media, Conditioned ; Female ; Hip Prosthesis ; Humans ; Investigative techniques, diagnostic techniques (general aspects) ; Male ; Medical sciences ; Microscopy, Electron, Scanning ; Middle Aged ; Molecular Weight ; Osteoarticular system. Muscles ; Osteoblasts - pathology ; Osteoblasts - physiology ; Osteolysis - metabolism ; Osteosarcoma - pathology ; Particle Size ; Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques ; Polyethylenes ; Prosthesis Failure ; Thymidine - metabolism ; Tumor Cells, Cultured</subject><ispartof>Journal of bone and joint surgery. American volume, 1999-04, Vol.81 (4), p.452-61</ispartof><rights>Copyright 1999 by The Journal of Bone and Joint Surgery, Incorporated</rights><rights>1999 INIST-CNRS</rights><rights>Copyright Journal of Bone and Joint Surgery, Inc. Apr 1999</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5092-570cf322511468d0059d2d38f02fe1f8b35fe6538566c4cfaa0df15b163450cd3</citedby><cites>FETCH-LOGICAL-c5092-570cf322511468d0059d2d38f02fe1f8b35fe6538566c4cfaa0df15b163450cd3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=1769095$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10225790$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>DEAN, D D</creatorcontrib><creatorcontrib>SCHWARTZ, Z</creatorcontrib><creatorcontrib>LIU, Y</creatorcontrib><creatorcontrib>BLANCHARD, C R</creatorcontrib><creatorcontrib>AGRAWAL, C M</creatorcontrib><creatorcontrib>MABREY, J D</creatorcontrib><creatorcontrib>SYLVIA, V L</creatorcontrib><creatorcontrib>LOHMANN, C H</creatorcontrib><creatorcontrib>BOYAN, B D</creatorcontrib><title>The Effect of Ultra-High Molecular Weight Polyethylene Wear Debris on MG63 Osteosarcoma Cells in Vitro</title><title>Journal of bone and joint surgery. American volume</title><addtitle>J Bone Joint Surg Am</addtitle><description>BackgroundFocal osteolysis due to ultra-high molecular weight polyethylene wear debris involves effects on both bone resorption and bone formation. MethodsThe response of MG63 osteoblast-like osteosarcoma cells to ultra-high molecular weight polyethylene wear debris isolated by enzymatic digestion of granulomatous tissue obtained from the sites of failed total hip arthroplasties was examined. Scanning electron microscopy, particle-size analysis, and Fourier transform infrared spectroscopy were used to characterize the number, morphology, size distribution, and chemical composition of the particles. Cell response was assessed by adding particles at varying dilutions to confluent cultures and measuring changes in cell proliferation (number of cells and [H]-thymidine incorporation), osteoblast function (alkaline-phosphatase-specific activity and osteocalcin production), matrix production (collagen production and proteoglycan sulfation), and local cytokine production (prostaglandin-E2 production). ResultsThe mean size of the particles was 0.60 micrometer, and 95 percent of the particles had a size of less than 1.5 micrometers. The number of particles per gram of tissue ranged from 1.39 to 3.38 x 10. Three of the four batches of particles were endotoxin-free. Exposure of the cells to particles of wear debris significantly increased the number of cells (p &lt; 0.05) and the [H]-thymidine incorporation (p &lt; 0.05) in a dose-dependent manner. In contrast, the addition of particles decreased alkaline-phosphatase-specific activity and osteocalcin production. Collagen production and proteoglycan sulfation were also decreased, while prostaglandin-E2 synthesis was increased by the addition of particles. ConclusionsUltra-high molecular weight polyethylene particles isolated from human tissue stimulated osteoblast proliferation and prostaglandin-E2 production and inhibited cell differentiation and matrix production. These results indicate that particles of wear debris inhibit cell functions associated with bone formation and that osteoblasts may produce factors in response to wear debris that influence neighboring cells, such as osteoclasts and macrophages. Clinical RelevanceParticles of wear debris, especially ultra-high molecular weight polyethylene, have been implicated in the loosening of implants and the development of osteolysis. The present study shows that particles of ultra-high molecular weight polyethylene isolated from human tissue inhibit osteoblast functions associated with bone formation. In addition, particles of wear debris induced osteoblasts to secrete factors capable of influencing neighboring cells, such as osteoclasts and macrophages. These results suggest that osteoblasts may play a role in the cascade of events leading to granuloma formation, osteolysis, and failure of orthopaedic implants.</description><subject>Adult</subject><subject>Alkaline Phosphatase - metabolism</subject><subject>Biological and medical sciences</subject><subject>Cell Division</subject><subject>Collagen - biosynthesis</subject><subject>Culture Media, Conditioned</subject><subject>Female</subject><subject>Hip Prosthesis</subject><subject>Humans</subject><subject>Investigative techniques, diagnostic techniques (general aspects)</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Microscopy, Electron, Scanning</subject><subject>Middle Aged</subject><subject>Molecular Weight</subject><subject>Osteoarticular system. 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American volume</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>DEAN, D D</au><au>SCHWARTZ, Z</au><au>LIU, Y</au><au>BLANCHARD, C R</au><au>AGRAWAL, C M</au><au>MABREY, J D</au><au>SYLVIA, V L</au><au>LOHMANN, C H</au><au>BOYAN, B D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Effect of Ultra-High Molecular Weight Polyethylene Wear Debris on MG63 Osteosarcoma Cells in Vitro</atitle><jtitle>Journal of bone and joint surgery. American volume</jtitle><addtitle>J Bone Joint Surg Am</addtitle><date>1999-04</date><risdate>1999</risdate><volume>81</volume><issue>4</issue><spage>452</spage><epage>61</epage><pages>452-61</pages><issn>0021-9355</issn><eissn>1535-1386</eissn><coden>JBJSA3</coden><abstract>BackgroundFocal osteolysis due to ultra-high molecular weight polyethylene wear debris involves effects on both bone resorption and bone formation. MethodsThe response of MG63 osteoblast-like osteosarcoma cells to ultra-high molecular weight polyethylene wear debris isolated by enzymatic digestion of granulomatous tissue obtained from the sites of failed total hip arthroplasties was examined. Scanning electron microscopy, particle-size analysis, and Fourier transform infrared spectroscopy were used to characterize the number, morphology, size distribution, and chemical composition of the particles. Cell response was assessed by adding particles at varying dilutions to confluent cultures and measuring changes in cell proliferation (number of cells and [H]-thymidine incorporation), osteoblast function (alkaline-phosphatase-specific activity and osteocalcin production), matrix production (collagen production and proteoglycan sulfation), and local cytokine production (prostaglandin-E2 production). ResultsThe mean size of the particles was 0.60 micrometer, and 95 percent of the particles had a size of less than 1.5 micrometers. The number of particles per gram of tissue ranged from 1.39 to 3.38 x 10. Three of the four batches of particles were endotoxin-free. Exposure of the cells to particles of wear debris significantly increased the number of cells (p &lt; 0.05) and the [H]-thymidine incorporation (p &lt; 0.05) in a dose-dependent manner. In contrast, the addition of particles decreased alkaline-phosphatase-specific activity and osteocalcin production. Collagen production and proteoglycan sulfation were also decreased, while prostaglandin-E2 synthesis was increased by the addition of particles. ConclusionsUltra-high molecular weight polyethylene particles isolated from human tissue stimulated osteoblast proliferation and prostaglandin-E2 production and inhibited cell differentiation and matrix production. These results indicate that particles of wear debris inhibit cell functions associated with bone formation and that osteoblasts may produce factors in response to wear debris that influence neighboring cells, such as osteoclasts and macrophages. Clinical RelevanceParticles of wear debris, especially ultra-high molecular weight polyethylene, have been implicated in the loosening of implants and the development of osteolysis. The present study shows that particles of ultra-high molecular weight polyethylene isolated from human tissue inhibit osteoblast functions associated with bone formation. In addition, particles of wear debris induced osteoblasts to secrete factors capable of influencing neighboring cells, such as osteoclasts and macrophages. These results suggest that osteoblasts may play a role in the cascade of events leading to granuloma formation, osteolysis, and failure of orthopaedic implants.</abstract><cop>Boston, MA</cop><pub>Copyright by The Journal of Bone and Joint Surgery, Incorporated</pub><pmid>10225790</pmid><doi>10.2106/00004623-199904000-00002</doi><tpages>-390</tpages><edition>American volume</edition></addata></record>
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subjects Adult
Alkaline Phosphatase - metabolism
Biological and medical sciences
Cell Division
Collagen - biosynthesis
Culture Media, Conditioned
Female
Hip Prosthesis
Humans
Investigative techniques, diagnostic techniques (general aspects)
Male
Medical sciences
Microscopy, Electron, Scanning
Middle Aged
Molecular Weight
Osteoarticular system. Muscles
Osteoblasts - pathology
Osteoblasts - physiology
Osteolysis - metabolism
Osteosarcoma - pathology
Particle Size
Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques
Polyethylenes
Prosthesis Failure
Thymidine - metabolism
Tumor Cells, Cultured
title The Effect of Ultra-High Molecular Weight Polyethylene Wear Debris on MG63 Osteosarcoma Cells in Vitro
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