Effects of injurious compression on matrix turnover around individual cells in calf articular cartilage explants
The effects of mechanical injury on the metabolism of cartilage matrix are of interest for understanding the pathogenesis of osteoarthrosis and the development of strategies for cartilage repair. The purpose of the present study was to examine the effects of injury on matrix turnover in a calf artic...
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Veröffentlicht in: | Journal of orthopaedic research 1998-07, Vol.16 (4), p.490-499 |
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description | The effects of mechanical injury on the metabolism of cartilage matrix are of interest for understanding the pathogenesis of osteoarthrosis and the development of strategies for cartilage repair. The purpose of the present study was to examine the effects of injury on matrix turnover in a calf articular cartilage explant system for which the effects of mechanical loading on cell activity and the cell‐mediated pathways of matrix metabolism are already well characterized. New methods of quantitative autoradiography were used in combination with established biochemical and biomechanical techniques for the analysis of cell and matrix responses to acute mechanical injury, with particular attention to the processes of localized matrix turnover in the cell‐associated matrices of individual chondrocytes. Matrix deposition and turnover around cells in control explants was spatially dependent, with the highest rates of proteoglycan deposition and tunrtover arid the lowest rates of collagen deposition (as indicated by [3H]proline autoradiography) occurring in the pericellular matrix. Injurious compression was associated with (a) an abrupt decrease in the tensile load‐carrying capacity of the collagen matrix, apparently associated with mechanical failure of the tissue, (b) a considerable but subtotal decrease in cell viability, marked by the emergence of an apparently inactive cell population interspersed within catabolically active but abnormally large cells, and (c) sustained, elevated rates of protcoglycan turnover, particularly in the cell‐associated matrices of apparently viable cells, which involved the increased release of aggregating species in addition to a spectrum of degradation fragments that were also in controls. These results may represent an in vitro model for the responses of chondrocytes and the cartilage extracellular matrix to mechanical injury. |
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The purpose of the present study was to examine the effects of injury on matrix turnover in a calf articular cartilage explant system for which the effects of mechanical loading on cell activity and the cell‐mediated pathways of matrix metabolism are already well characterized. New methods of quantitative autoradiography were used in combination with established biochemical and biomechanical techniques for the analysis of cell and matrix responses to acute mechanical injury, with particular attention to the processes of localized matrix turnover in the cell‐associated matrices of individual chondrocytes. Matrix deposition and turnover around cells in control explants was spatially dependent, with the highest rates of proteoglycan deposition and tunrtover arid the lowest rates of collagen deposition (as indicated by [3H]proline autoradiography) occurring in the pericellular matrix. Injurious compression was associated with (a) an abrupt decrease in the tensile load‐carrying capacity of the collagen matrix, apparently associated with mechanical failure of the tissue, (b) a considerable but subtotal decrease in cell viability, marked by the emergence of an apparently inactive cell population interspersed within catabolically active but abnormally large cells, and (c) sustained, elevated rates of protcoglycan turnover, particularly in the cell‐associated matrices of apparently viable cells, which involved the increased release of aggregating species in addition to a spectrum of degradation fragments that were also in controls. These results may represent an in vitro model for the responses of chondrocytes and the cartilage extracellular matrix to mechanical injury.</description><identifier>ISSN: 0736-0266</identifier><identifier>EISSN: 1554-527X</identifier><identifier>DOI: 10.1002/jor.1100160415</identifier><identifier>PMID: 9747792</identifier><identifier>CODEN: JOREDR</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Animals ; Autoradiography ; Biochemistry ; Biomechanics ; Cartilage, Articular - cytology ; Cartilage, Articular - injuries ; Cartilage, Articular - metabolism ; Cattle ; Cell Survival ; Cells ; Chondrocytes - metabolism ; Collagen ; Collagen - metabolism ; Compression testing ; Cytology ; Extracellular Matrix - metabolism ; In Vitro Techniques ; Knee Joint - physiology ; Metabolism ; Pressure ; Proline - metabolism ; Proteoglycans - metabolism ; Space life sciences ; Stress, Mechanical ; Tensile Strength</subject><ispartof>Journal of orthopaedic research, 1998-07, Vol.16 (4), p.490-499</ispartof><rights>Copyright © 1998 Orthopaedic Research Society</rights><rights>Copyright Journal of Bone and Joint Surgery, Inc. Jul 1998</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5315-50067dcb0e6c18620143a4c4fe817406e7c7371d25769b0f2489fe17ee4c1ad33</citedby><cites>FETCH-LOGICAL-c5315-50067dcb0e6c18620143a4c4fe817406e7c7371d25769b0f2489fe17ee4c1ad33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjor.1100160415$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjor.1100160415$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,778,782,1414,27907,27908,45557,45558</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9747792$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Quinn, Thomas M.</creatorcontrib><creatorcontrib>Grodzinsky, Alan J.</creatorcontrib><creatorcontrib>Hunziker, Ernst B.</creatorcontrib><creatorcontrib>Sandy, John D.</creatorcontrib><title>Effects of injurious compression on matrix turnover around individual cells in calf articular cartilage explants</title><title>Journal of orthopaedic research</title><addtitle>J. Orthop. Res</addtitle><description>The effects of mechanical injury on the metabolism of cartilage matrix are of interest for understanding the pathogenesis of osteoarthrosis and the development of strategies for cartilage repair. The purpose of the present study was to examine the effects of injury on matrix turnover in a calf articular cartilage explant system for which the effects of mechanical loading on cell activity and the cell‐mediated pathways of matrix metabolism are already well characterized. New methods of quantitative autoradiography were used in combination with established biochemical and biomechanical techniques for the analysis of cell and matrix responses to acute mechanical injury, with particular attention to the processes of localized matrix turnover in the cell‐associated matrices of individual chondrocytes. Matrix deposition and turnover around cells in control explants was spatially dependent, with the highest rates of proteoglycan deposition and tunrtover arid the lowest rates of collagen deposition (as indicated by [3H]proline autoradiography) occurring in the pericellular matrix. Injurious compression was associated with (a) an abrupt decrease in the tensile load‐carrying capacity of the collagen matrix, apparently associated with mechanical failure of the tissue, (b) a considerable but subtotal decrease in cell viability, marked by the emergence of an apparently inactive cell population interspersed within catabolically active but abnormally large cells, and (c) sustained, elevated rates of protcoglycan turnover, particularly in the cell‐associated matrices of apparently viable cells, which involved the increased release of aggregating species in addition to a spectrum of degradation fragments that were also in controls. These results may represent an in vitro model for the responses of chondrocytes and the cartilage extracellular matrix to mechanical injury.</description><subject>Animals</subject><subject>Autoradiography</subject><subject>Biochemistry</subject><subject>Biomechanics</subject><subject>Cartilage, Articular - cytology</subject><subject>Cartilage, Articular - injuries</subject><subject>Cartilage, Articular - metabolism</subject><subject>Cattle</subject><subject>Cell Survival</subject><subject>Cells</subject><subject>Chondrocytes - metabolism</subject><subject>Collagen</subject><subject>Collagen - metabolism</subject><subject>Compression testing</subject><subject>Cytology</subject><subject>Extracellular Matrix - metabolism</subject><subject>In Vitro Techniques</subject><subject>Knee Joint - physiology</subject><subject>Metabolism</subject><subject>Pressure</subject><subject>Proline - metabolism</subject><subject>Proteoglycans - metabolism</subject><subject>Space life sciences</subject><subject>Stress, Mechanical</subject><subject>Tensile Strength</subject><issn>0736-0266</issn><issn>1554-527X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqFUUtv1DAQthCoLIUrN6SIA7dsPX4mR1S15bFqBQK1N8vrTJCXJA52Urb_Hq921YpeKlnyjL-HPPMR8hboEihlJ5sQl5ArUFSAfEYWIKUoJdM3z8mCaq5KypR6SV6ltKGUamDVETmqtdC6ZgsynrUtuikVoS38sJmjD3MqXOjHiCn5MBT59HaKfltMcxzCLcbCxjAPTeY3_tY3s-0Kh12X8kPhbNdmfPJu7mzMbS47-wsL3I6dHab0mrxobZfwzeE-Jj_Pz36cfipXVxefTz-uSic5yFJSqnTj1hSVg0oxCoJb4USLFWhBFWqnuYaGSa3qNW2ZqOoWQSMKB7bh_Jh82PuOMfyZMU2m92n3TTtgHtFoXjPJJDxJZMCVrkFl4vtHxE3IG8lDGMazERV857bck1wMKUVszRh9b-OdAWp2gWVRNA-BZcG7g-u87rG5px8Syni9x__6Du-ecDNfrr7_513utT5NuL3X2vjbqLw9aa4vLwy_-Xr-Daprs-L_AE-0sbE</recordid><startdate>199807</startdate><enddate>199807</enddate><creator>Quinn, Thomas M.</creator><creator>Grodzinsky, Alan J.</creator><creator>Hunziker, Ernst B.</creator><creator>Sandy, John D.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Blackwell Publishing Ltd</general><scope>BSCLL</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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>199807</creationdate><title>Effects of injurious compression on matrix turnover around individual cells in calf articular cartilage explants</title><author>Quinn, Thomas M. ; Grodzinsky, Alan J. ; Hunziker, Ernst B. ; Sandy, John D.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5315-50067dcb0e6c18620143a4c4fe817406e7c7371d25769b0f2489fe17ee4c1ad33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Animals</topic><topic>Autoradiography</topic><topic>Biochemistry</topic><topic>Biomechanics</topic><topic>Cartilage, Articular - cytology</topic><topic>Cartilage, Articular - injuries</topic><topic>Cartilage, Articular - metabolism</topic><topic>Cattle</topic><topic>Cell Survival</topic><topic>Cells</topic><topic>Chondrocytes - metabolism</topic><topic>Collagen</topic><topic>Collagen - metabolism</topic><topic>Compression testing</topic><topic>Cytology</topic><topic>Extracellular Matrix - metabolism</topic><topic>In Vitro Techniques</topic><topic>Knee Joint - physiology</topic><topic>Metabolism</topic><topic>Pressure</topic><topic>Proline - metabolism</topic><topic>Proteoglycans - metabolism</topic><topic>Space life sciences</topic><topic>Stress, Mechanical</topic><topic>Tensile Strength</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Quinn, Thomas M.</creatorcontrib><creatorcontrib>Grodzinsky, Alan J.</creatorcontrib><creatorcontrib>Hunziker, Ernst B.</creatorcontrib><creatorcontrib>Sandy, John D.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database (ProQuest)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of orthopaedic research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Quinn, Thomas M.</au><au>Grodzinsky, Alan J.</au><au>Hunziker, Ernst B.</au><au>Sandy, John D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of injurious compression on matrix turnover around individual cells in calf articular cartilage explants</atitle><jtitle>Journal of orthopaedic research</jtitle><addtitle>J. Orthop. Res</addtitle><date>1998-07</date><risdate>1998</risdate><volume>16</volume><issue>4</issue><spage>490</spage><epage>499</epage><pages>490-499</pages><issn>0736-0266</issn><eissn>1554-527X</eissn><coden>JOREDR</coden><abstract>The effects of mechanical injury on the metabolism of cartilage matrix are of interest for understanding the pathogenesis of osteoarthrosis and the development of strategies for cartilage repair. The purpose of the present study was to examine the effects of injury on matrix turnover in a calf articular cartilage explant system for which the effects of mechanical loading on cell activity and the cell‐mediated pathways of matrix metabolism are already well characterized. New methods of quantitative autoradiography were used in combination with established biochemical and biomechanical techniques for the analysis of cell and matrix responses to acute mechanical injury, with particular attention to the processes of localized matrix turnover in the cell‐associated matrices of individual chondrocytes. Matrix deposition and turnover around cells in control explants was spatially dependent, with the highest rates of proteoglycan deposition and tunrtover arid the lowest rates of collagen deposition (as indicated by [3H]proline autoradiography) occurring in the pericellular matrix. Injurious compression was associated with (a) an abrupt decrease in the tensile load‐carrying capacity of the collagen matrix, apparently associated with mechanical failure of the tissue, (b) a considerable but subtotal decrease in cell viability, marked by the emergence of an apparently inactive cell population interspersed within catabolically active but abnormally large cells, and (c) sustained, elevated rates of protcoglycan turnover, particularly in the cell‐associated matrices of apparently viable cells, which involved the increased release of aggregating species in addition to a spectrum of degradation fragments that were also in controls. These results may represent an in vitro model for the responses of chondrocytes and the cartilage extracellular matrix to mechanical injury.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>9747792</pmid><doi>10.1002/jor.1100160415</doi><tpages>10</tpages></addata></record> |
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subjects | Animals Autoradiography Biochemistry Biomechanics Cartilage, Articular - cytology Cartilage, Articular - injuries Cartilage, Articular - metabolism Cattle Cell Survival Cells Chondrocytes - metabolism Collagen Collagen - metabolism Compression testing Cytology Extracellular Matrix - metabolism In Vitro Techniques Knee Joint - physiology Metabolism Pressure Proline - metabolism Proteoglycans - metabolism Space life sciences Stress, Mechanical Tensile Strength |
title | Effects of injurious compression on matrix turnover around individual cells in calf articular cartilage explants |
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