Substrate porosity enhances chondrocyte attachment, spreading, and cartilage tissue formation in vitro
Tissue engineering is being explored as a new approach to treat damaged cartilage. As the biomaterial used may influence tissue formation, the effects of substrate geometry on chondrocyte behavior in vitro were examined. Articular chondrocytes were isolated and cultured on the surface of smooth, rou...
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Veröffentlicht in: | Journal of biomedical materials research 2006-09, Vol.78A (4), p.676-683 |
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description | Tissue engineering is being explored as a new approach to treat damaged cartilage. As the biomaterial used may influence tissue formation, the effects of substrate geometry on chondrocyte behavior in vitro were examined. Articular chondrocytes were isolated and cultured on the surface of smooth, rough, porous‐coated, and fully porous Ti‐6Al‐4V substrates. The percentage of chondrocytes that attached to each substrate at 24 h was determined. After 24 and 72 h, chondrocytes were visualized by scanning electron microscopy and cell areas were measured. Collagen and proteoglycan accumulation within the first 24 h was determined by incorporation with [3H]‐proline and [35S]‐SO4, respectively. Chondrocyte attachment as well as matrix accumulation was enhanced as substrate surface area increased. Cell areas on the fully porous substrate were over four times greater than on any other substrate by 72 h in culture. After 8 weeks in culture, a continuous layer of cartilaginous tissue formed only on the surface of the fully porous substrate. This suggests that fully porous Ti‐6Al‐4V substrates provide the conditions that favor cartilage tissue formation by influencing cell attachment and extent of cell spreading. Understanding how substrate porosity influences chondrocyte behavior may help identify methods to further enhance cartilage tissue formation in vitro. © 2006 Wiley Periodicals, Inc. J Biomed Mater Res, 2006 |
doi_str_mv | 10.1002/jbm.a.30746 |
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G. ; Pilliar, R. M. ; Kandel, R. A.</creator><creatorcontrib>Spiteri, C. G. ; Pilliar, R. M. ; Kandel, R. A.</creatorcontrib><description>Tissue engineering is being explored as a new approach to treat damaged cartilage. As the biomaterial used may influence tissue formation, the effects of substrate geometry on chondrocyte behavior in vitro were examined. Articular chondrocytes were isolated and cultured on the surface of smooth, rough, porous‐coated, and fully porous Ti‐6Al‐4V substrates. The percentage of chondrocytes that attached to each substrate at 24 h was determined. After 24 and 72 h, chondrocytes were visualized by scanning electron microscopy and cell areas were measured. Collagen and proteoglycan accumulation within the first 24 h was determined by incorporation with [3H]‐proline and [35S]‐SO4, respectively. Chondrocyte attachment as well as matrix accumulation was enhanced as substrate surface area increased. Cell areas on the fully porous substrate were over four times greater than on any other substrate by 72 h in culture. After 8 weeks in culture, a continuous layer of cartilaginous tissue formed only on the surface of the fully porous substrate. This suggests that fully porous Ti‐6Al‐4V substrates provide the conditions that favor cartilage tissue formation by influencing cell attachment and extent of cell spreading. Understanding how substrate porosity influences chondrocyte behavior may help identify methods to further enhance cartilage tissue formation in vitro. © 2006 Wiley Periodicals, Inc. J Biomed Mater Res, 2006</description><identifier>ISSN: 1549-3296</identifier><identifier>ISSN: 0021-9304</identifier><identifier>EISSN: 1552-4965</identifier><identifier>EISSN: 1097-4636</identifier><identifier>DOI: 10.1002/jbm.a.30746</identifier><identifier>PMID: 16739175</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Animals ; cartilage tissue engineering ; Cartilage, Articular - cytology ; Cartilage, Articular - ultrastructure ; Cattle ; Cell Adhesion ; cell morphology ; Cells, Cultured ; Chondrocytes - cytology ; Chondrocytes - ultrastructure ; In Vitro Techniques ; Microscopy, Electron, Scanning ; substrate porosity ; Titanium ; titanium alloy</subject><ispartof>Journal of biomedical materials research, 2006-09, Vol.78A (4), p.676-683</ispartof><rights>Copyright © 2006 Wiley Periodicals, Inc.</rights><rights>2006 Wiley Periodicals, Inc. 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M.</creatorcontrib><creatorcontrib>Kandel, R. A.</creatorcontrib><title>Substrate porosity enhances chondrocyte attachment, spreading, and cartilage tissue formation in vitro</title><title>Journal of biomedical materials research</title><addtitle>J. Biomed. Mater. Res</addtitle><description>Tissue engineering is being explored as a new approach to treat damaged cartilage. As the biomaterial used may influence tissue formation, the effects of substrate geometry on chondrocyte behavior in vitro were examined. Articular chondrocytes were isolated and cultured on the surface of smooth, rough, porous‐coated, and fully porous Ti‐6Al‐4V substrates. The percentage of chondrocytes that attached to each substrate at 24 h was determined. After 24 and 72 h, chondrocytes were visualized by scanning electron microscopy and cell areas were measured. Collagen and proteoglycan accumulation within the first 24 h was determined by incorporation with [3H]‐proline and [35S]‐SO4, respectively. Chondrocyte attachment as well as matrix accumulation was enhanced as substrate surface area increased. Cell areas on the fully porous substrate were over four times greater than on any other substrate by 72 h in culture. After 8 weeks in culture, a continuous layer of cartilaginous tissue formed only on the surface of the fully porous substrate. This suggests that fully porous Ti‐6Al‐4V substrates provide the conditions that favor cartilage tissue formation by influencing cell attachment and extent of cell spreading. Understanding how substrate porosity influences chondrocyte behavior may help identify methods to further enhance cartilage tissue formation in vitro. © 2006 Wiley Periodicals, Inc. J Biomed Mater Res, 2006</description><subject>Animals</subject><subject>cartilage tissue engineering</subject><subject>Cartilage, Articular - cytology</subject><subject>Cartilage, Articular - ultrastructure</subject><subject>Cattle</subject><subject>Cell Adhesion</subject><subject>cell morphology</subject><subject>Cells, Cultured</subject><subject>Chondrocytes - cytology</subject><subject>Chondrocytes - ultrastructure</subject><subject>In Vitro Techniques</subject><subject>Microscopy, Electron, Scanning</subject><subject>substrate porosity</subject><subject>Titanium</subject><subject>titanium alloy</subject><issn>1549-3296</issn><issn>0021-9304</issn><issn>1552-4965</issn><issn>1097-4636</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkT1vFDEURUcIREKgokeuaMgs_p5xCREJoBCKgCgtj_0m6zBjb2wPYf89DrtARypb9rlHT-82zXOCVwRj-vp6mFdmxXDH5YPmkAhBW66keHh356plVMmD5knO1xWWWNDHzQGRHVOkE4fNeLkMuSRTAG1iitmXLYKwNsFCRnYdg0vRbuuvKcXY9QyhHKO8SWCcD1fHyASHrEnFT-YKUPE5L4DGmGZTfAzIB_TDlxSfNo9GM2V4tj-Pmq-n776cvG_PP599OHlz3lpex2yFGwkzAggfewuGSoVp75yg1gxAnGB24B0G2o2OW9FRWd97SS0Qy7AkAztqXu68mxRvFshFzz5bmCYTIC5Zy14RSji-F6RKSNUpdS9IFBe4x6yCr3agrWvMCUa9SX42aasJ1ndF6VqUNvp3UZV-sdcuwwzuH7tvpgJkB9z6Cbb_c-mPbz_9kba7jM8Ffv7NmPRdV20n9LeLM02poPxSKX3BfgHcha7X</recordid><startdate>20060915</startdate><enddate>20060915</enddate><creator>Spiteri, C. G.</creator><creator>Pilliar, R. M.</creator><creator>Kandel, R. A.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</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>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7SR</scope><scope>7TB</scope><scope>7U5</scope><scope>8BQ</scope><scope>F28</scope><scope>JG9</scope><scope>L7M</scope><scope>7X8</scope></search><sort><creationdate>20060915</creationdate><title>Substrate porosity enhances chondrocyte attachment, spreading, and cartilage tissue formation in vitro</title><author>Spiteri, C. G. ; Pilliar, R. M. ; Kandel, R. A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4296-5df13a5e14f8cea269028dd52cabe1d53cb470e27fd4c5726cab862ce1c3061b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Animals</topic><topic>cartilage tissue engineering</topic><topic>Cartilage, Articular - cytology</topic><topic>Cartilage, Articular - ultrastructure</topic><topic>Cattle</topic><topic>Cell Adhesion</topic><topic>cell morphology</topic><topic>Cells, Cultured</topic><topic>Chondrocytes - cytology</topic><topic>Chondrocytes - ultrastructure</topic><topic>In Vitro Techniques</topic><topic>Microscopy, Electron, Scanning</topic><topic>substrate porosity</topic><topic>Titanium</topic><topic>titanium alloy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Spiteri, C. G.</creatorcontrib><creatorcontrib>Pilliar, R. M.</creatorcontrib><creatorcontrib>Kandel, R. 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G.</au><au>Pilliar, R. M.</au><au>Kandel, R. A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Substrate porosity enhances chondrocyte attachment, spreading, and cartilage tissue formation in vitro</atitle><jtitle>Journal of biomedical materials research</jtitle><addtitle>J. Biomed. Mater. Res</addtitle><date>2006-09-15</date><risdate>2006</risdate><volume>78A</volume><issue>4</issue><spage>676</spage><epage>683</epage><pages>676-683</pages><issn>1549-3296</issn><issn>0021-9304</issn><eissn>1552-4965</eissn><eissn>1097-4636</eissn><abstract>Tissue engineering is being explored as a new approach to treat damaged cartilage. As the biomaterial used may influence tissue formation, the effects of substrate geometry on chondrocyte behavior in vitro were examined. Articular chondrocytes were isolated and cultured on the surface of smooth, rough, porous‐coated, and fully porous Ti‐6Al‐4V substrates. The percentage of chondrocytes that attached to each substrate at 24 h was determined. After 24 and 72 h, chondrocytes were visualized by scanning electron microscopy and cell areas were measured. Collagen and proteoglycan accumulation within the first 24 h was determined by incorporation with [3H]‐proline and [35S]‐SO4, respectively. Chondrocyte attachment as well as matrix accumulation was enhanced as substrate surface area increased. Cell areas on the fully porous substrate were over four times greater than on any other substrate by 72 h in culture. After 8 weeks in culture, a continuous layer of cartilaginous tissue formed only on the surface of the fully porous substrate. This suggests that fully porous Ti‐6Al‐4V substrates provide the conditions that favor cartilage tissue formation by influencing cell attachment and extent of cell spreading. Understanding how substrate porosity influences chondrocyte behavior may help identify methods to further enhance cartilage tissue formation in vitro. © 2006 Wiley Periodicals, Inc. J Biomed Mater Res, 2006</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>16739175</pmid><doi>10.1002/jbm.a.30746</doi><tpages>8</tpages></addata></record> |
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subjects | Animals cartilage tissue engineering Cartilage, Articular - cytology Cartilage, Articular - ultrastructure Cattle Cell Adhesion cell morphology Cells, Cultured Chondrocytes - cytology Chondrocytes - ultrastructure In Vitro Techniques Microscopy, Electron, Scanning substrate porosity Titanium titanium alloy |
title | Substrate porosity enhances chondrocyte attachment, spreading, and cartilage tissue formation in vitro |
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