Development of a cell-derived matrix: Effects of epidermal growth factor in chemically defined culture
Extracellular matrices without animal components and with high mechanical strength are needed for the development of the next generation of viable skin replacements. The goal of this study was to determine the optimal concentration of epidermal growth factor (EGF) to maximize the strength and collag...
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Veröffentlicht in: | Journal of biomedical materials research. Part A 2010-02, Vol.92A (2), p.533-541 |
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description | Extracellular matrices without animal components and with high mechanical strength are needed for the development of the next generation of viable skin replacements. The goal of this study was to determine the optimal concentration of epidermal growth factor (EGF) to maximize the strength and collagen content of cell‐derived matrix (CDM) produced by fibroblasts in vitro in serum‐free media. Scaffold‐free CDM samples were produced by human dermal fibroblasts in the presence of 0–50 ng/mL EGF in chemically defined media. After 21 days of culture, a membrane inflation system was used to measure the biaxial tensile strength, failure stretch ratio, and thickness of each treatment group. The fibroblasts treated with 5 ng/mL EGF produced the thickest matrix (270 μm). A thinner (130 μm) matrix, produced when the fibroblasts were treated with 0.5 ng/mL, had an ultimate tensile strength (895 kPa), greater than two times that of the other treatment groups. The fibroblasts treated with 0.5 ng/mL also had the highest collagen density (23.5 mg/cm3). Fibroblasts stimulated with the lowest (0.05 ng/mL) and highest (50 ng/mL) concentrations of EGF produced significantly weaker matrices and lower collagen densities. There was no significant correlation between UTS and collagen density suggesting that mechanisms other than density contribute to the strength of the matrix. Taken together, these data indicate that the optimal EGF concentration depends upon the relative importance of matrix strength and volume in a given application and that 0.5–5.0 ng/mL EGF promotes production of a robust extracellular matrix in only 3 weeks. © 2009 Wiley Periodicals, Inc. J Biomed Mater Res, 2010 |
doi_str_mv | 10.1002/jbm.a.32369 |
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The goal of this study was to determine the optimal concentration of epidermal growth factor (EGF) to maximize the strength and collagen content of cell‐derived matrix (CDM) produced by fibroblasts in vitro in serum‐free media. Scaffold‐free CDM samples were produced by human dermal fibroblasts in the presence of 0–50 ng/mL EGF in chemically defined media. After 21 days of culture, a membrane inflation system was used to measure the biaxial tensile strength, failure stretch ratio, and thickness of each treatment group. The fibroblasts treated with 5 ng/mL EGF produced the thickest matrix (270 μm). A thinner (130 μm) matrix, produced when the fibroblasts were treated with 0.5 ng/mL, had an ultimate tensile strength (895 kPa), greater than two times that of the other treatment groups. The fibroblasts treated with 0.5 ng/mL also had the highest collagen density (23.5 mg/cm3). Fibroblasts stimulated with the lowest (0.05 ng/mL) and highest (50 ng/mL) concentrations of EGF produced significantly weaker matrices and lower collagen densities. There was no significant correlation between UTS and collagen density suggesting that mechanisms other than density contribute to the strength of the matrix. Taken together, these data indicate that the optimal EGF concentration depends upon the relative importance of matrix strength and volume in a given application and that 0.5–5.0 ng/mL EGF promotes production of a robust extracellular matrix in only 3 weeks. © 2009 Wiley Periodicals, Inc. J Biomed Mater Res, 2010</description><identifier>ISSN: 1549-3296</identifier><identifier>ISSN: 1552-4965</identifier><identifier>EISSN: 1552-4965</identifier><identifier>DOI: 10.1002/jbm.a.32369</identifier><identifier>PMID: 19235212</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Algorithms ; biaxial mechanical characterization ; Biological and medical sciences ; Biotechnology ; Cell Proliferation - drug effects ; cell-derived matrix ; Cells, Cultured ; Collagen - biosynthesis ; Collagen - chemistry ; Collagens ; Connective Tissue - growth & development ; Culture ; Culture Media ; Density ; epidermal growth factor ; Epidermal Growth Factor - pharmacology ; extracellular matrix ; Extracellular Matrix - drug effects ; Fibroblasts ; Fibroblasts - drug effects ; Fibroblasts - physiology ; Fundamental and applied biological sciences. Psychology ; Health. Pharmaceutical industry ; Humans ; Industrial applications and implications. Economical aspects ; Mathematical analysis ; Matrices ; Media ; Medical sciences ; Miscellaneous ; serum-free culture ; Skin - cytology ; Skin - drug effects ; Skin plastic surgery ; Strength ; Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases ; Technology. Biomaterials. Equipments ; Tensile Strength</subject><ispartof>Journal of biomedical materials research. 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Part A</title><addtitle>J. Biomed. Mater. Res</addtitle><description>Extracellular matrices without animal components and with high mechanical strength are needed for the development of the next generation of viable skin replacements. The goal of this study was to determine the optimal concentration of epidermal growth factor (EGF) to maximize the strength and collagen content of cell‐derived matrix (CDM) produced by fibroblasts in vitro in serum‐free media. Scaffold‐free CDM samples were produced by human dermal fibroblasts in the presence of 0–50 ng/mL EGF in chemically defined media. After 21 days of culture, a membrane inflation system was used to measure the biaxial tensile strength, failure stretch ratio, and thickness of each treatment group. The fibroblasts treated with 5 ng/mL EGF produced the thickest matrix (270 μm). A thinner (130 μm) matrix, produced when the fibroblasts were treated with 0.5 ng/mL, had an ultimate tensile strength (895 kPa), greater than two times that of the other treatment groups. The fibroblasts treated with 0.5 ng/mL also had the highest collagen density (23.5 mg/cm3). Fibroblasts stimulated with the lowest (0.05 ng/mL) and highest (50 ng/mL) concentrations of EGF produced significantly weaker matrices and lower collagen densities. There was no significant correlation between UTS and collagen density suggesting that mechanisms other than density contribute to the strength of the matrix. Taken together, these data indicate that the optimal EGF concentration depends upon the relative importance of matrix strength and volume in a given application and that 0.5–5.0 ng/mL EGF promotes production of a robust extracellular matrix in only 3 weeks. © 2009 Wiley Periodicals, Inc. J Biomed Mater Res, 2010</description><subject>Algorithms</subject><subject>biaxial mechanical characterization</subject><subject>Biological and medical sciences</subject><subject>Biotechnology</subject><subject>Cell Proliferation - drug effects</subject><subject>cell-derived matrix</subject><subject>Cells, Cultured</subject><subject>Collagen - biosynthesis</subject><subject>Collagen - chemistry</subject><subject>Collagens</subject><subject>Connective Tissue - growth & development</subject><subject>Culture</subject><subject>Culture Media</subject><subject>Density</subject><subject>epidermal growth factor</subject><subject>Epidermal Growth Factor - pharmacology</subject><subject>extracellular matrix</subject><subject>Extracellular Matrix - drug effects</subject><subject>Fibroblasts</subject><subject>Fibroblasts - drug effects</subject><subject>Fibroblasts - physiology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Health. Pharmaceutical industry</subject><subject>Humans</subject><subject>Industrial applications and implications. Economical aspects</subject><subject>Mathematical analysis</subject><subject>Matrices</subject><subject>Media</subject><subject>Medical sciences</subject><subject>Miscellaneous</subject><subject>serum-free culture</subject><subject>Skin - cytology</subject><subject>Skin - drug effects</subject><subject>Skin plastic surgery</subject><subject>Strength</subject><subject>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</subject><subject>Technology. Biomaterials. Equipments</subject><subject>Tensile Strength</subject><issn>1549-3296</issn><issn>1552-4965</issn><issn>1552-4965</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqN0stv1DAQB-AIgWhpOXFHviCQULZ-P3qDpRRQH5cijpbjjKlLHoudtN3_noRdyq3tybb8eX6yZoriFcELgjE9uKrahVswyqR5UuwSIWjJjRRP5z03JaNG7hQvcr6asMSCPi92iKFMUEJ3i_AJrqHpVy10A-oDcshD05Q1pHgNNWrdkOLtIToKAfyQZwGrON22rkE_U38zXKLg_NAnFDvkL6GN3jXNGtUQYjcV8GMzjAn2i2fBNRlebte94vvno4vll_Lk_Pjr8sNJ6QXVppQU1yCJ8ibIuqq1ow40U1zX3oDwWlfVdNAYMAjOpfOG8OCwpsxgVgXN9oq3m7qr1P8eIQ-2jXn-keugH7PVmmHCMeMPS2mE1lLgB6ViTGku1Zz-7l5JpCKMG8MfR6lQUs357zfUpz7nBMGuUmxdWluC7TwBdpoA6-zfCZj0623hsWqh_m-3LZ_Amy1weepVSK7zMd85SjkWzJDJkY27iQ2s78u03z6e_gsvN29iHuD27o1Lv6xUTAn74-zYsgtmzvCpskv2B3Mu1hc</recordid><startdate>201002</startdate><enddate>201002</enddate><creator>Throm, Angela M.</creator><creator>Liu, Wai-Ching</creator><creator>Lock, Chi-Hung</creator><creator>Billiar, Kristen L.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Blackwell</general><scope>BSCLL</scope><scope>IQODW</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>7SR</scope><scope>7TB</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>F28</scope><scope>FR3</scope><scope>JG9</scope><scope>L7M</scope><scope>7X8</scope><scope>7QO</scope><scope>P64</scope></search><sort><creationdate>201002</creationdate><title>Development of a cell-derived matrix: Effects of epidermal growth factor in chemically defined culture</title><author>Throm, Angela M. ; Liu, Wai-Ching ; Lock, Chi-Hung ; Billiar, Kristen L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5289-620de617c9f6dbd8a2ae83748dc9e5c88bb74880e0e5446ac914fa0823903bf83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Algorithms</topic><topic>biaxial mechanical characterization</topic><topic>Biological and medical sciences</topic><topic>Biotechnology</topic><topic>Cell Proliferation - drug effects</topic><topic>cell-derived matrix</topic><topic>Cells, Cultured</topic><topic>Collagen - biosynthesis</topic><topic>Collagen - chemistry</topic><topic>Collagens</topic><topic>Connective Tissue - growth & development</topic><topic>Culture</topic><topic>Culture Media</topic><topic>Density</topic><topic>epidermal growth factor</topic><topic>Epidermal Growth Factor - pharmacology</topic><topic>extracellular matrix</topic><topic>Extracellular Matrix - drug effects</topic><topic>Fibroblasts</topic><topic>Fibroblasts - drug effects</topic><topic>Fibroblasts - physiology</topic><topic>Fundamental and applied biological sciences. 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Part A</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Throm, Angela M.</au><au>Liu, Wai-Ching</au><au>Lock, Chi-Hung</au><au>Billiar, Kristen L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Development of a cell-derived matrix: Effects of epidermal growth factor in chemically defined culture</atitle><jtitle>Journal of biomedical materials research. Part A</jtitle><addtitle>J. Biomed. Mater. Res</addtitle><date>2010-02</date><risdate>2010</risdate><volume>92A</volume><issue>2</issue><spage>533</spage><epage>541</epage><pages>533-541</pages><issn>1549-3296</issn><issn>1552-4965</issn><eissn>1552-4965</eissn><abstract>Extracellular matrices without animal components and with high mechanical strength are needed for the development of the next generation of viable skin replacements. The goal of this study was to determine the optimal concentration of epidermal growth factor (EGF) to maximize the strength and collagen content of cell‐derived matrix (CDM) produced by fibroblasts in vitro in serum‐free media. Scaffold‐free CDM samples were produced by human dermal fibroblasts in the presence of 0–50 ng/mL EGF in chemically defined media. After 21 days of culture, a membrane inflation system was used to measure the biaxial tensile strength, failure stretch ratio, and thickness of each treatment group. The fibroblasts treated with 5 ng/mL EGF produced the thickest matrix (270 μm). A thinner (130 μm) matrix, produced when the fibroblasts were treated with 0.5 ng/mL, had an ultimate tensile strength (895 kPa), greater than two times that of the other treatment groups. The fibroblasts treated with 0.5 ng/mL also had the highest collagen density (23.5 mg/cm3). Fibroblasts stimulated with the lowest (0.05 ng/mL) and highest (50 ng/mL) concentrations of EGF produced significantly weaker matrices and lower collagen densities. There was no significant correlation between UTS and collagen density suggesting that mechanisms other than density contribute to the strength of the matrix. Taken together, these data indicate that the optimal EGF concentration depends upon the relative importance of matrix strength and volume in a given application and that 0.5–5.0 ng/mL EGF promotes production of a robust extracellular matrix in only 3 weeks. © 2009 Wiley Periodicals, Inc. J Biomed Mater Res, 2010</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>19235212</pmid><doi>10.1002/jbm.a.32369</doi><tpages>9</tpages></addata></record> |
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subjects | Algorithms biaxial mechanical characterization Biological and medical sciences Biotechnology Cell Proliferation - drug effects cell-derived matrix Cells, Cultured Collagen - biosynthesis Collagen - chemistry Collagens Connective Tissue - growth & development Culture Culture Media Density epidermal growth factor Epidermal Growth Factor - pharmacology extracellular matrix Extracellular Matrix - drug effects Fibroblasts Fibroblasts - drug effects Fibroblasts - physiology Fundamental and applied biological sciences. Psychology Health. Pharmaceutical industry Humans Industrial applications and implications. Economical aspects Mathematical analysis Matrices Media Medical sciences Miscellaneous serum-free culture Skin - cytology Skin - drug effects Skin plastic surgery Strength Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases Technology. Biomaterials. Equipments Tensile Strength |
title | Development of a cell-derived matrix: Effects of epidermal growth factor in chemically defined culture |
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