Chondrocyte repopulation of the zone of death induced by osteochondral harvest

Summary Objective Harvesting osteochondral grafts results in a zone of chondrocyte death (ZCD) in and around the periphery of the graft, creating a barrier for chondrocytes to migrate to the graft periphery, thus limiting cartilage-to-cartilage healing. The purpose of this study was to repopulate th...

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Veröffentlicht in:Osteoarthritis and cartilage 2011-02, Vol.19 (2), p.242-248
Hauptverfasser: McGregor, A.J, Amsden, B.G, Waldman, S.D
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container_title Osteoarthritis and cartilage
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creator McGregor, A.J
Amsden, B.G
Waldman, S.D
description Summary Objective Harvesting osteochondral grafts results in a zone of chondrocyte death (ZCD) in and around the periphery of the graft, creating a barrier for chondrocytes to migrate to the graft periphery, thus limiting cartilage-to-cartilage healing. The purpose of this study was to repopulate the induced ZCD through the combined effects of collagenase treatment and delivery of a chemotactic agent. Design In bovine cartilage, the ZCD induced by the OATS™ osteochondral harvesting system was determined, followed by a corresponding collagenase treatment to penetrate the developed ZCD. The chemotactic potential of platelet derived growth factor (PDGF-bb), insulin-like growth factor I (IGF-I), and basic fibroblast growth factor (bFGF) (2.5–100 ng/mL) was then assessed using a modified Boyden chamber assay to select an appropriate agent to induce chondrocyte migration. Afterwards, the combined effects of collagenase treatment and chondrocyte chemotaxis on the repopulation of an induced ZCD were examined in cartilage explants over a 4-week-period. Results The OATS™ osteochondral harvesting system induced a significant ZCD (173 μm, 95% CI: [72–274 μm]) in the grafts. Chondrocyte chemotaxis was induced by all agents investigated at concentrations greater than 25 ng/mL. After 4 weeks in culture, collagenase treatment alone reduced the ZCD by approximately 40% relative to untreated explants. Coupling the collagenase treatment with 25 ng/mL IGF-I reduced the ZCD by approximately 80% relative to untreated explants, and 65% relative to explants treated only with collagenase. Conclusion Treating cartilage explants with collagenase and 25 ng/mL IGF-I resulted in a decreased ZCD after a 4-week-period, and increased chondrocyte density within the induced ZCD.
doi_str_mv 10.1016/j.joca.2010.11.008
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The purpose of this study was to repopulate the induced ZCD through the combined effects of collagenase treatment and delivery of a chemotactic agent. Design In bovine cartilage, the ZCD induced by the OATS™ osteochondral harvesting system was determined, followed by a corresponding collagenase treatment to penetrate the developed ZCD. The chemotactic potential of platelet derived growth factor (PDGF-bb), insulin-like growth factor I (IGF-I), and basic fibroblast growth factor (bFGF) (2.5–100 ng/mL) was then assessed using a modified Boyden chamber assay to select an appropriate agent to induce chondrocyte migration. Afterwards, the combined effects of collagenase treatment and chondrocyte chemotaxis on the repopulation of an induced ZCD were examined in cartilage explants over a 4-week-period. Results The OATS™ osteochondral harvesting system induced a significant ZCD (173 μm, 95% CI: [72–274 μm]) in the grafts. Chondrocyte chemotaxis was induced by all agents investigated at concentrations greater than 25 ng/mL. After 4 weeks in culture, collagenase treatment alone reduced the ZCD by approximately 40% relative to untreated explants. Coupling the collagenase treatment with 25 ng/mL IGF-I reduced the ZCD by approximately 80% relative to untreated explants, and 65% relative to explants treated only with collagenase. Conclusion Treating cartilage explants with collagenase and 25 ng/mL IGF-I resulted in a decreased ZCD after a 4-week-period, and increased chondrocyte density within the induced ZCD.</description><identifier>ISSN: 1063-4584</identifier><identifier>EISSN: 1522-9653</identifier><identifier>DOI: 10.1016/j.joca.2010.11.008</identifier><identifier>PMID: 21112408</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Animals ; Cartilage - drug effects ; Cartilage - pathology ; Cattle ; Cell Movement - drug effects ; Cell Movement - physiology ; Chemotaxis ; Chondrocyte ; Chondrocytes - drug effects ; Chondrocytes - physiology ; Diffusion Chambers, Culture ; Fibroblast Growth Factor 2 - pharmacology ; Insulin-Like Growth Factor I - pharmacology ; Osteochondral transfer ; Platelet-Derived Growth Factor - pharmacology ; Proto-Oncogene Proteins c-sis ; Repopulation ; Rheumatology ; Zone of chondrocyte death</subject><ispartof>Osteoarthritis and cartilage, 2011-02, Vol.19 (2), p.242-248</ispartof><rights>Osteoarthritis Research Society International</rights><rights>2010 Osteoarthritis Research Society International</rights><rights>Copyright © 2010 Osteoarthritis Research Society International. Published by Elsevier Ltd. 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The purpose of this study was to repopulate the induced ZCD through the combined effects of collagenase treatment and delivery of a chemotactic agent. Design In bovine cartilage, the ZCD induced by the OATS™ osteochondral harvesting system was determined, followed by a corresponding collagenase treatment to penetrate the developed ZCD. The chemotactic potential of platelet derived growth factor (PDGF-bb), insulin-like growth factor I (IGF-I), and basic fibroblast growth factor (bFGF) (2.5–100 ng/mL) was then assessed using a modified Boyden chamber assay to select an appropriate agent to induce chondrocyte migration. Afterwards, the combined effects of collagenase treatment and chondrocyte chemotaxis on the repopulation of an induced ZCD were examined in cartilage explants over a 4-week-period. Results The OATS™ osteochondral harvesting system induced a significant ZCD (173 μm, 95% CI: [72–274 μm]) in the grafts. Chondrocyte chemotaxis was induced by all agents investigated at concentrations greater than 25 ng/mL. After 4 weeks in culture, collagenase treatment alone reduced the ZCD by approximately 40% relative to untreated explants. Coupling the collagenase treatment with 25 ng/mL IGF-I reduced the ZCD by approximately 80% relative to untreated explants, and 65% relative to explants treated only with collagenase. Conclusion Treating cartilage explants with collagenase and 25 ng/mL IGF-I resulted in a decreased ZCD after a 4-week-period, and increased chondrocyte density within the induced ZCD.</description><subject>Animals</subject><subject>Cartilage - drug effects</subject><subject>Cartilage - pathology</subject><subject>Cattle</subject><subject>Cell Movement - drug effects</subject><subject>Cell Movement - physiology</subject><subject>Chemotaxis</subject><subject>Chondrocyte</subject><subject>Chondrocytes - drug effects</subject><subject>Chondrocytes - physiology</subject><subject>Diffusion Chambers, Culture</subject><subject>Fibroblast Growth Factor 2 - pharmacology</subject><subject>Insulin-Like Growth Factor I - pharmacology</subject><subject>Osteochondral transfer</subject><subject>Platelet-Derived Growth Factor - pharmacology</subject><subject>Proto-Oncogene Proteins c-sis</subject><subject>Repopulation</subject><subject>Rheumatology</subject><subject>Zone of chondrocyte death</subject><issn>1063-4584</issn><issn>1522-9653</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kUtLxDAUhYMovv-AC-nOVcebx9QURJDBF4gu1HXIJLdMaqcZk3Zg_PWmzujChatcwjnncr9DyAmFEQVanNej2hs9YjB80BGA3CL7dMxYXhZjvp1mKHguxlLskYMYawDglMIu2WOUUiZA7pOnycy3Nniz6jALuPCLvtGd823mq6ybYfbpWxxmi7qbZa61vUGbTVeZjx168-3WTTbTYYmxOyI7lW4iHm_eQ_J2e_M6uc8fn-8eJtePuRkz6HJpZKlZJVDCRVnI0kCluTDC6spqBGmZ1iVCgQUTVoqKIRMMJUdqCuSc8UNyts5dBP_Rp8Vq7qLBptEt-j4qKWSKBV4mJVsrTfAxBqzUIri5DitFQQ0YVa0GjGrAqChVCWMynW7i--kc7a_lh1sSXK4FmI5cOgwqGodtQuMCmk5Z7_7Pv_pjN41rndHNO64w1r4PbcKnqIpMgXoZihx6pEOFpZD8C_6ZmPQ</recordid><startdate>20110201</startdate><enddate>20110201</enddate><creator>McGregor, A.J</creator><creator>Amsden, B.G</creator><creator>Waldman, S.D</creator><general>Elsevier Ltd</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20110201</creationdate><title>Chondrocyte repopulation of the zone of death induced by osteochondral harvest</title><author>McGregor, A.J ; Amsden, B.G ; Waldman, S.D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c520t-8c89a2f4e8079689c0fa34c4dafdae08d2aa9e06e624d84f2e242e83e1c6e3323</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Animals</topic><topic>Cartilage - drug effects</topic><topic>Cartilage - pathology</topic><topic>Cattle</topic><topic>Cell Movement - drug effects</topic><topic>Cell Movement - physiology</topic><topic>Chemotaxis</topic><topic>Chondrocyte</topic><topic>Chondrocytes - drug effects</topic><topic>Chondrocytes - physiology</topic><topic>Diffusion Chambers, Culture</topic><topic>Fibroblast Growth Factor 2 - pharmacology</topic><topic>Insulin-Like Growth Factor I - pharmacology</topic><topic>Osteochondral transfer</topic><topic>Platelet-Derived Growth Factor - pharmacology</topic><topic>Proto-Oncogene Proteins c-sis</topic><topic>Repopulation</topic><topic>Rheumatology</topic><topic>Zone of chondrocyte death</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>McGregor, A.J</creatorcontrib><creatorcontrib>Amsden, B.G</creatorcontrib><creatorcontrib>Waldman, S.D</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Osteoarthritis and cartilage</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>McGregor, A.J</au><au>Amsden, B.G</au><au>Waldman, S.D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Chondrocyte repopulation of the zone of death induced by osteochondral harvest</atitle><jtitle>Osteoarthritis and cartilage</jtitle><addtitle>Osteoarthritis Cartilage</addtitle><date>2011-02-01</date><risdate>2011</risdate><volume>19</volume><issue>2</issue><spage>242</spage><epage>248</epage><pages>242-248</pages><issn>1063-4584</issn><eissn>1522-9653</eissn><abstract>Summary Objective Harvesting osteochondral grafts results in a zone of chondrocyte death (ZCD) in and around the periphery of the graft, creating a barrier for chondrocytes to migrate to the graft periphery, thus limiting cartilage-to-cartilage healing. The purpose of this study was to repopulate the induced ZCD through the combined effects of collagenase treatment and delivery of a chemotactic agent. Design In bovine cartilage, the ZCD induced by the OATS™ osteochondral harvesting system was determined, followed by a corresponding collagenase treatment to penetrate the developed ZCD. The chemotactic potential of platelet derived growth factor (PDGF-bb), insulin-like growth factor I (IGF-I), and basic fibroblast growth factor (bFGF) (2.5–100 ng/mL) was then assessed using a modified Boyden chamber assay to select an appropriate agent to induce chondrocyte migration. Afterwards, the combined effects of collagenase treatment and chondrocyte chemotaxis on the repopulation of an induced ZCD were examined in cartilage explants over a 4-week-period. Results The OATS™ osteochondral harvesting system induced a significant ZCD (173 μm, 95% CI: [72–274 μm]) in the grafts. Chondrocyte chemotaxis was induced by all agents investigated at concentrations greater than 25 ng/mL. After 4 weeks in culture, collagenase treatment alone reduced the ZCD by approximately 40% relative to untreated explants. Coupling the collagenase treatment with 25 ng/mL IGF-I reduced the ZCD by approximately 80% relative to untreated explants, and 65% relative to explants treated only with collagenase. Conclusion Treating cartilage explants with collagenase and 25 ng/mL IGF-I resulted in a decreased ZCD after a 4-week-period, and increased chondrocyte density within the induced ZCD.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>21112408</pmid><doi>10.1016/j.joca.2010.11.008</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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subjects Animals
Cartilage - drug effects
Cartilage - pathology
Cattle
Cell Movement - drug effects
Cell Movement - physiology
Chemotaxis
Chondrocyte
Chondrocytes - drug effects
Chondrocytes - physiology
Diffusion Chambers, Culture
Fibroblast Growth Factor 2 - pharmacology
Insulin-Like Growth Factor I - pharmacology
Osteochondral transfer
Platelet-Derived Growth Factor - pharmacology
Proto-Oncogene Proteins c-sis
Repopulation
Rheumatology
Zone of chondrocyte death
title Chondrocyte repopulation of the zone of death induced by osteochondral harvest
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