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Type II collagen-chondroitin sulfate-hyaluronan scaffold cross-linked by genipin for cartilage tissue engineering
Owing to of the limited repair capacity of articular cartilage, it is essential to develop tissue-engineered cartilage for patients suffering from joint disease. Chondroitin sulfate (CS) and hyaluronan (HA) are the components of the cartilage extracellular matrix (ECM) and are known to influence the...
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Published in: | Journal of bioscience and bioengineering 2009-02, Vol.107 (2), p.177-182 |
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description | Owing to of the limited repair capacity of articular cartilage, it is essential to develop tissue-engineered cartilage for patients suffering from joint disease. Chondroitin sulfate (CS) and hyaluronan (HA) are the components of the cartilage extracellular matrix (ECM) and are known to influence the proliferation and differentiation of chondrocytes. Scaffolds composed of type-II collagen, CS, and HA may create an environment that can preserve the normal phenotype of cells to promote regeneration of cartilage-like constructs. In this investigation, we prepared and characterized 3-dimensional type-II collagen scaffolds both with and without HA and CS. Porous composite scaffolds fabricated by freeze-drying showed interconnected pores with mean diameters of 140
±
30 µm and porosities of 92–95% after cross-linking with genipin. After a 14-day
in vitro culture, morphologically round chondrocytes were found to be uniformly distributed throughout the sponges. Expression of genes of aggrecan, type-II collagen and cartilage oligomeric matrix protein (COMP) was statistically and significantly increased on scaffolds with CS and HA than those without CS and HA. Furthermore, there was a markedly greater accumulation of proteoglycans (PGs) on the scaffolds with CS and HA. |
doi_str_mv | 10.1016/j.jbiosc.2008.09.020 |
format | article |
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±
30 µm and porosities of 92–95% after cross-linking with genipin. After a 14-day
in vitro culture, morphologically round chondrocytes were found to be uniformly distributed throughout the sponges. Expression of genes of aggrecan, type-II collagen and cartilage oligomeric matrix protein (COMP) was statistically and significantly increased on scaffolds with CS and HA than those without CS and HA. Furthermore, there was a markedly greater accumulation of proteoglycans (PGs) on the scaffolds with CS and HA.</description><identifier>ISSN: 1389-1723</identifier><identifier>EISSN: 1347-4421</identifier><identifier>DOI: 10.1016/j.jbiosc.2008.09.020</identifier><identifier>PMID: 19217557</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>ACIDE HYALURONIQUE ; ACIDO HIALURONICO ; ANIMAL TISSUES ; ARN MENSAJERO ; ARN MESSAGER ; Biological and medical sciences ; Biotechnology ; Cartilage, Articular - cytology ; Chondroitin sulfate ; COLAGENO ; COLLAGEN ; Collagen Type II - chemistry ; COLLAGENE ; ENVIRONMENT ; ENVIRONNEMENT ; EXPRESION GENICA ; EXPRESSION DES GENES ; FREEZE DRYING ; Fundamental and applied biological sciences. Psychology ; GENE EXPRESSION ; Genipin ; Humans ; Hyaline cartilage ; Hyaluronan ; HYALURONIC ACID ; Hyaluronic Acid - chemistry ; Iridoid Glycosides ; Iridoids - chemistry ; LIOFILIZACION ; LYOPHILISATION ; MEDIO AMBIENTE ; MESSENGER RNA ; Microscopy, Electron, Scanning ; REGENERACION ; REGENERATION ; TEJIDOS ANIMALES ; TISSU ANIMAL ; Tissue Engineering ; Type II collagen</subject><ispartof>Journal of bioscience and bioengineering, 2009-02, Vol.107 (2), p.177-182</ispartof><rights>2008 The Society for Biotechnology, Japan</rights><rights>2009 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c467t-23f03b5bc09ebdbf5b16a5c34220d4b827ba4dabc243a1666f19966b23a780043</citedby><cites>FETCH-LOGICAL-c467t-23f03b5bc09ebdbf5b16a5c34220d4b827ba4dabc243a1666f19966b23a780043</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21283844$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19217557$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ko, Chih-Sheng</creatorcontrib><creatorcontrib>Huang, Jui-Pin</creatorcontrib><creatorcontrib>Huang, Chia-Wen</creatorcontrib><creatorcontrib>Chu, I-Ming</creatorcontrib><title>Type II collagen-chondroitin sulfate-hyaluronan scaffold cross-linked by genipin for cartilage tissue engineering</title><title>Journal of bioscience and bioengineering</title><addtitle>J Biosci Bioeng</addtitle><description>Owing to of the limited repair capacity of articular cartilage, it is essential to develop tissue-engineered cartilage for patients suffering from joint disease. Chondroitin sulfate (CS) and hyaluronan (HA) are the components of the cartilage extracellular matrix (ECM) and are known to influence the proliferation and differentiation of chondrocytes. Scaffolds composed of type-II collagen, CS, and HA may create an environment that can preserve the normal phenotype of cells to promote regeneration of cartilage-like constructs. In this investigation, we prepared and characterized 3-dimensional type-II collagen scaffolds both with and without HA and CS. Porous composite scaffolds fabricated by freeze-drying showed interconnected pores with mean diameters of 140
±
30 µm and porosities of 92–95% after cross-linking with genipin. After a 14-day
in vitro culture, morphologically round chondrocytes were found to be uniformly distributed throughout the sponges. Expression of genes of aggrecan, type-II collagen and cartilage oligomeric matrix protein (COMP) was statistically and significantly increased on scaffolds with CS and HA than those without CS and HA. Furthermore, there was a markedly greater accumulation of proteoglycans (PGs) on the scaffolds with CS and HA.</description><subject>ACIDE HYALURONIQUE</subject><subject>ACIDO HIALURONICO</subject><subject>ANIMAL TISSUES</subject><subject>ARN MENSAJERO</subject><subject>ARN MESSAGER</subject><subject>Biological and medical sciences</subject><subject>Biotechnology</subject><subject>Cartilage, Articular - cytology</subject><subject>Chondroitin sulfate</subject><subject>COLAGENO</subject><subject>COLLAGEN</subject><subject>Collagen Type II - chemistry</subject><subject>COLLAGENE</subject><subject>ENVIRONMENT</subject><subject>ENVIRONNEMENT</subject><subject>EXPRESION GENICA</subject><subject>EXPRESSION DES GENES</subject><subject>FREEZE DRYING</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>GENE EXPRESSION</subject><subject>Genipin</subject><subject>Humans</subject><subject>Hyaline cartilage</subject><subject>Hyaluronan</subject><subject>HYALURONIC ACID</subject><subject>Hyaluronic Acid - chemistry</subject><subject>Iridoid Glycosides</subject><subject>Iridoids - chemistry</subject><subject>LIOFILIZACION</subject><subject>LYOPHILISATION</subject><subject>MEDIO AMBIENTE</subject><subject>MESSENGER RNA</subject><subject>Microscopy, Electron, Scanning</subject><subject>REGENERACION</subject><subject>REGENERATION</subject><subject>TEJIDOS ANIMALES</subject><subject>TISSU ANIMAL</subject><subject>Tissue Engineering</subject><subject>Type II collagen</subject><issn>1389-1723</issn><issn>1347-4421</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNqFkU1v1DAQhiMEoqXwDwDlArcs44_YyQWpqvhYVAkO5WzZznjrJWtv7QRp_z0OWcENTrbs552Zd96qeklgQ4CId_vN3viY7YYCdBvoN0DhUXVJGJcN55Q8Xu5d3xBJ2UX1LOc9AJEgydPqgvSUyLaVl9XD3emI9XZb2ziOeoehsfcxDCn6yYc6z6PTEzb3Jz3OKQZdnqx2Lo5DbVPMuRl9-IFDbU510fpj0biYaqvT5Jdy9eRznrHGsPMBMfmwe149cXrM-OJ8XlXfP364u_nc3H79tL25vm0sF3JqKHPATGss9GgG41pDhG4t45TCwE1HpdF80MZSzjQRQjjS90IYyrTsADi7qt6udY8pPsyYJ3Xw2WJxGTDOWQnRU9FC91-QApOiZbSAfAV_W0_o1DH5g04nRUAtmai9WjNRSyYKelUyKbLX5_qzOeDwV3QOoQBvzoAu2x1d0sH6_IejhHas44ujVyvndFR6lwrz5Vvp1JdgCV8avV__saz1p8eksvUYLA4-oZ3UEP2_J_0FN8G2UA</recordid><startdate>20090201</startdate><enddate>20090201</enddate><creator>Ko, Chih-Sheng</creator><creator>Huang, Jui-Pin</creator><creator>Huang, Chia-Wen</creator><creator>Chu, I-Ming</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>FBQ</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>7QO</scope><scope>7QP</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20090201</creationdate><title>Type II collagen-chondroitin sulfate-hyaluronan scaffold cross-linked by genipin for cartilage tissue engineering</title><author>Ko, Chih-Sheng ; Huang, Jui-Pin ; Huang, Chia-Wen ; Chu, I-Ming</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c467t-23f03b5bc09ebdbf5b16a5c34220d4b827ba4dabc243a1666f19966b23a780043</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>ACIDE HYALURONIQUE</topic><topic>ACIDO HIALURONICO</topic><topic>ANIMAL TISSUES</topic><topic>ARN MENSAJERO</topic><topic>ARN MESSAGER</topic><topic>Biological and medical sciences</topic><topic>Biotechnology</topic><topic>Cartilage, Articular - cytology</topic><topic>Chondroitin sulfate</topic><topic>COLAGENO</topic><topic>COLLAGEN</topic><topic>Collagen Type II - chemistry</topic><topic>COLLAGENE</topic><topic>ENVIRONMENT</topic><topic>ENVIRONNEMENT</topic><topic>EXPRESION GENICA</topic><topic>EXPRESSION DES GENES</topic><topic>FREEZE DRYING</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>GENE EXPRESSION</topic><topic>Genipin</topic><topic>Humans</topic><topic>Hyaline cartilage</topic><topic>Hyaluronan</topic><topic>HYALURONIC ACID</topic><topic>Hyaluronic Acid - chemistry</topic><topic>Iridoid Glycosides</topic><topic>Iridoids - chemistry</topic><topic>LIOFILIZACION</topic><topic>LYOPHILISATION</topic><topic>MEDIO AMBIENTE</topic><topic>MESSENGER RNA</topic><topic>Microscopy, Electron, Scanning</topic><topic>REGENERACION</topic><topic>REGENERATION</topic><topic>TEJIDOS ANIMALES</topic><topic>TISSU ANIMAL</topic><topic>Tissue Engineering</topic><topic>Type II collagen</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ko, Chih-Sheng</creatorcontrib><creatorcontrib>Huang, Jui-Pin</creatorcontrib><creatorcontrib>Huang, Chia-Wen</creatorcontrib><creatorcontrib>Chu, I-Ming</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of bioscience and bioengineering</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ko, Chih-Sheng</au><au>Huang, Jui-Pin</au><au>Huang, Chia-Wen</au><au>Chu, I-Ming</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Type II collagen-chondroitin sulfate-hyaluronan scaffold cross-linked by genipin for cartilage tissue engineering</atitle><jtitle>Journal of bioscience and bioengineering</jtitle><addtitle>J Biosci Bioeng</addtitle><date>2009-02-01</date><risdate>2009</risdate><volume>107</volume><issue>2</issue><spage>177</spage><epage>182</epage><pages>177-182</pages><issn>1389-1723</issn><eissn>1347-4421</eissn><abstract>Owing to of the limited repair capacity of articular cartilage, it is essential to develop tissue-engineered cartilage for patients suffering from joint disease. Chondroitin sulfate (CS) and hyaluronan (HA) are the components of the cartilage extracellular matrix (ECM) and are known to influence the proliferation and differentiation of chondrocytes. Scaffolds composed of type-II collagen, CS, and HA may create an environment that can preserve the normal phenotype of cells to promote regeneration of cartilage-like constructs. In this investigation, we prepared and characterized 3-dimensional type-II collagen scaffolds both with and without HA and CS. Porous composite scaffolds fabricated by freeze-drying showed interconnected pores with mean diameters of 140
±
30 µm and porosities of 92–95% after cross-linking with genipin. After a 14-day
in vitro culture, morphologically round chondrocytes were found to be uniformly distributed throughout the sponges. Expression of genes of aggrecan, type-II collagen and cartilage oligomeric matrix protein (COMP) was statistically and significantly increased on scaffolds with CS and HA than those without CS and HA. Furthermore, there was a markedly greater accumulation of proteoglycans (PGs) on the scaffolds with CS and HA.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>19217557</pmid><doi>10.1016/j.jbiosc.2008.09.020</doi><tpages>6</tpages></addata></record> |
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subjects | ACIDE HYALURONIQUE ACIDO HIALURONICO ANIMAL TISSUES ARN MENSAJERO ARN MESSAGER Biological and medical sciences Biotechnology Cartilage, Articular - cytology Chondroitin sulfate COLAGENO COLLAGEN Collagen Type II - chemistry COLLAGENE ENVIRONMENT ENVIRONNEMENT EXPRESION GENICA EXPRESSION DES GENES FREEZE DRYING Fundamental and applied biological sciences. Psychology GENE EXPRESSION Genipin Humans Hyaline cartilage Hyaluronan HYALURONIC ACID Hyaluronic Acid - chemistry Iridoid Glycosides Iridoids - chemistry LIOFILIZACION LYOPHILISATION MEDIO AMBIENTE MESSENGER RNA Microscopy, Electron, Scanning REGENERACION REGENERATION TEJIDOS ANIMALES TISSU ANIMAL Tissue Engineering Type II collagen |
title | Type II collagen-chondroitin sulfate-hyaluronan scaffold cross-linked by genipin for cartilage tissue engineering |
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