Chondrogenic potential of stem cells derived from amniotic fluid, adipose tissue, or bone marrow encapsulated in fibrin gels containing TGF-β3

Abstract In this study, several types of hMSCs, derived from bone marrow, adipose tissue, or amniotic fluid, were encapsulated in a fibrin hydrogel mixed with TGF-β3 and then evaluated for their capacity for differentiation in vitro and in vivo . For determination of stem cell differentiation, RT-PC...

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Veröffentlicht in:Biomaterials 2011-11, Vol.32 (32), p.8139-8149
Hauptverfasser: Park, Ji Sun, Shim, Myung-Sun, Shim, Sung Han, Yang, Han Na, Jeon, Su Yeon, Woo, Dae Gyun, Lee, Dong Ryul, Yoon, Tae Ki, Park, Keun-Hong
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container_end_page 8149
container_issue 32
container_start_page 8139
container_title Biomaterials
container_volume 32
creator Park, Ji Sun
Shim, Myung-Sun
Shim, Sung Han
Yang, Han Na
Jeon, Su Yeon
Woo, Dae Gyun
Lee, Dong Ryul
Yoon, Tae Ki
Park, Keun-Hong
description Abstract In this study, several types of hMSCs, derived from bone marrow, adipose tissue, or amniotic fluid, were encapsulated in a fibrin hydrogel mixed with TGF-β3 and then evaluated for their capacity for differentiation in vitro and in vivo . For determination of stem cell differentiation, RT-PCR, real time quantitative PCR (qPCR), histology, and immunohistochemical assays were used for analysis of chondrogenesis. Using these analysis methods, several of the cultured hMSCS were found to highly express genes and proteins specific to cartilage forming tissues. Additionally, similar trends in expression were found in tissue recovered from nude mice transplanted with several types of hMSCs encapsulated in a fibrin hydrogel containing TGF-β3. The results of both in vitro and in vivo analyses showed that cultured or transplanted hMSCs mixed with TGF-β3 in a fibrin hydrogel differentiated into chondrocytes, suggesting that these cells would be suitable for reconstruction of hyaline articular cartilage.
doi_str_mv 10.1016/j.biomaterials.2011.07.043
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For determination of stem cell differentiation, RT-PCR, real time quantitative PCR (qPCR), histology, and immunohistochemical assays were used for analysis of chondrogenesis. Using these analysis methods, several of the cultured hMSCS were found to highly express genes and proteins specific to cartilage forming tissues. Additionally, similar trends in expression were found in tissue recovered from nude mice transplanted with several types of hMSCs encapsulated in a fibrin hydrogel containing TGF-β3. The results of both in vitro and in vivo analyses showed that cultured or transplanted hMSCs mixed with TGF-β3 in a fibrin hydrogel differentiated into chondrocytes, suggesting that these cells would be suitable for reconstruction of hyaline articular cartilage.</description><identifier>ISSN: 0142-9612</identifier><identifier>EISSN: 1878-5905</identifier><identifier>DOI: 10.1016/j.biomaterials.2011.07.043</identifier><identifier>PMID: 21840589</identifier><language>eng</language><publisher>Netherlands: Elsevier Ltd</publisher><subject>Adipose Tissue - cytology ; Advanced Basic Science ; Amniotic Fluid - cytology ; Animals ; Bone Marrow Cells - cytology ; Bone Marrow Cells - drug effects ; Cartilage ; Cartilage - drug effects ; Cartilage - metabolism ; Cells, Cultured ; Cells, Immobilized - cytology ; Chondrogenesis ; Chondrogenesis - drug effects ; Collagen Type I - metabolism ; Collagen Type II - metabolism ; Dentistry ; Fibrin ; Fibrin - pharmacology ; Gels ; Glycosaminoglycans - metabolism ; hMSC ; Humans ; Immunohistochemistry ; Immunophenotyping ; Mesenchymal Stem Cell Transplantation ; Mesenchymal Stromal Cells - cytology ; Mice ; Mice, Nude ; Organ Specificity - drug effects ; Reverse Transcriptase Polymerase Chain Reaction ; TGF-β3 ; Transforming Growth Factor beta3 - pharmacology</subject><ispartof>Biomaterials, 2011-11, Vol.32 (32), p.8139-8149</ispartof><rights>Elsevier Ltd</rights><rights>2011 Elsevier Ltd</rights><rights>Copyright © 2011 Elsevier Ltd. 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For determination of stem cell differentiation, RT-PCR, real time quantitative PCR (qPCR), histology, and immunohistochemical assays were used for analysis of chondrogenesis. Using these analysis methods, several of the cultured hMSCS were found to highly express genes and proteins specific to cartilage forming tissues. Additionally, similar trends in expression were found in tissue recovered from nude mice transplanted with several types of hMSCs encapsulated in a fibrin hydrogel containing TGF-β3. 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Shim, Myung-Sun ; Shim, Sung Han ; Yang, Han Na ; Jeon, Su Yeon ; Woo, Dae Gyun ; Lee, Dong Ryul ; Yoon, Tae Ki ; Park, Keun-Hong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c415t-d4819aedd3420962df580e0a8a2fafd5ca61f5a6cc4ad50c9c7b8e0d875d4ce53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Adipose Tissue - cytology</topic><topic>Advanced Basic Science</topic><topic>Amniotic Fluid - cytology</topic><topic>Animals</topic><topic>Bone Marrow Cells - cytology</topic><topic>Bone Marrow Cells - drug effects</topic><topic>Cartilage</topic><topic>Cartilage - drug effects</topic><topic>Cartilage - metabolism</topic><topic>Cells, Cultured</topic><topic>Cells, Immobilized - cytology</topic><topic>Chondrogenesis</topic><topic>Chondrogenesis - drug effects</topic><topic>Collagen Type I - metabolism</topic><topic>Collagen Type II - metabolism</topic><topic>Dentistry</topic><topic>Fibrin</topic><topic>Fibrin - pharmacology</topic><topic>Gels</topic><topic>Glycosaminoglycans - metabolism</topic><topic>hMSC</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Immunophenotyping</topic><topic>Mesenchymal Stem Cell Transplantation</topic><topic>Mesenchymal Stromal Cells - cytology</topic><topic>Mice</topic><topic>Mice, Nude</topic><topic>Organ Specificity - drug effects</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>TGF-β3</topic><topic>Transforming Growth Factor beta3 - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Park, Ji Sun</creatorcontrib><creatorcontrib>Shim, Myung-Sun</creatorcontrib><creatorcontrib>Shim, Sung Han</creatorcontrib><creatorcontrib>Yang, Han Na</creatorcontrib><creatorcontrib>Jeon, Su Yeon</creatorcontrib><creatorcontrib>Woo, Dae Gyun</creatorcontrib><creatorcontrib>Lee, Dong Ryul</creatorcontrib><creatorcontrib>Yoon, Tae Ki</creatorcontrib><creatorcontrib>Park, Keun-Hong</creatorcontrib><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>Biomaterials</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Park, Ji Sun</au><au>Shim, Myung-Sun</au><au>Shim, Sung Han</au><au>Yang, Han Na</au><au>Jeon, Su Yeon</au><au>Woo, Dae Gyun</au><au>Lee, Dong Ryul</au><au>Yoon, Tae Ki</au><au>Park, Keun-Hong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Chondrogenic potential of stem cells derived from amniotic fluid, adipose tissue, or bone marrow encapsulated in fibrin gels containing TGF-β3</atitle><jtitle>Biomaterials</jtitle><addtitle>Biomaterials</addtitle><date>2011-11</date><risdate>2011</risdate><volume>32</volume><issue>32</issue><spage>8139</spage><epage>8149</epage><pages>8139-8149</pages><issn>0142-9612</issn><eissn>1878-5905</eissn><abstract>Abstract In this study, several types of hMSCs, derived from bone marrow, adipose tissue, or amniotic fluid, were encapsulated in a fibrin hydrogel mixed with TGF-β3 and then evaluated for their capacity for differentiation in vitro and in vivo . For determination of stem cell differentiation, RT-PCR, real time quantitative PCR (qPCR), histology, and immunohistochemical assays were used for analysis of chondrogenesis. Using these analysis methods, several of the cultured hMSCS were found to highly express genes and proteins specific to cartilage forming tissues. Additionally, similar trends in expression were found in tissue recovered from nude mice transplanted with several types of hMSCs encapsulated in a fibrin hydrogel containing TGF-β3. The results of both in vitro and in vivo analyses showed that cultured or transplanted hMSCs mixed with TGF-β3 in a fibrin hydrogel differentiated into chondrocytes, suggesting that these cells would be suitable for reconstruction of hyaline articular cartilage.</abstract><cop>Netherlands</cop><pub>Elsevier Ltd</pub><pmid>21840589</pmid><doi>10.1016/j.biomaterials.2011.07.043</doi><tpages>11</tpages></addata></record>
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subjects Adipose Tissue - cytology
Advanced Basic Science
Amniotic Fluid - cytology
Animals
Bone Marrow Cells - cytology
Bone Marrow Cells - drug effects
Cartilage
Cartilage - drug effects
Cartilage - metabolism
Cells, Cultured
Cells, Immobilized - cytology
Chondrogenesis
Chondrogenesis - drug effects
Collagen Type I - metabolism
Collagen Type II - metabolism
Dentistry
Fibrin
Fibrin - pharmacology
Gels
Glycosaminoglycans - metabolism
hMSC
Humans
Immunohistochemistry
Immunophenotyping
Mesenchymal Stem Cell Transplantation
Mesenchymal Stromal Cells - cytology
Mice
Mice, Nude
Organ Specificity - drug effects
Reverse Transcriptase Polymerase Chain Reaction
TGF-β3
Transforming Growth Factor beta3 - pharmacology
title Chondrogenic potential of stem cells derived from amniotic fluid, adipose tissue, or bone marrow encapsulated in fibrin gels containing TGF-β3
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