The collagen I mimetic peptide DGEA enhances an osteogenic phenotype in mesenchymal stem cells when presented from cell-encapsulating hydrogels
Interactions between cells and the extracellular matrix (ECM) are known to play critical roles in regulating cell phenotype. The identity of ECM ligands presented to mesenchymal stem cells (MSCs) has previously been shown to direct the cell fate commitment of these cells. To enhance osteogenic diffe...
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Veröffentlicht in: | Journal of biomedical materials research. Part A 2015-11, Vol.103 (11), p.3516-3525 |
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description | Interactions between cells and the extracellular matrix (ECM) are known to play critical roles in regulating cell phenotype. The identity of ECM ligands presented to mesenchymal stem cells (MSCs) has previously been shown to direct the cell fate commitment of these cells. To enhance osteogenic differentiation of MSCs, alginate hydrogels were prepared that present the DGEA ligand derived from collagen I. When presented from hydrogel surfaces in 2D, the DGEA ligand did not facilitate cell adhesion, while hydrogels presenting the RGD ligand derived from fibronectin did encourage cell adhesion and spreading. However, the osteogenic differentiation of MSCs encapsulated within alginate hydrogels presenting the DGEA ligand was enhanced when compared with unmodified alginate hydrogels and hydrogels presenting the RGD ligand. MSCs cultured in DGEA‐presenting gels exhibited increased levels of osteocalcin production and mineral deposition. These data suggest that the presentation of the collagen I‐derived DGEA ligand is a feasible approach for selectively inducing an osteogenic phenotype in encapsulated MSCs. © 2015 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 103A: 3516–3525, 2015. |
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The identity of ECM ligands presented to mesenchymal stem cells (MSCs) has previously been shown to direct the cell fate commitment of these cells. To enhance osteogenic differentiation of MSCs, alginate hydrogels were prepared that present the DGEA ligand derived from collagen I. When presented from hydrogel surfaces in 2D, the DGEA ligand did not facilitate cell adhesion, while hydrogels presenting the RGD ligand derived from fibronectin did encourage cell adhesion and spreading. However, the osteogenic differentiation of MSCs encapsulated within alginate hydrogels presenting the DGEA ligand was enhanced when compared with unmodified alginate hydrogels and hydrogels presenting the RGD ligand. MSCs cultured in DGEA‐presenting gels exhibited increased levels of osteocalcin production and mineral deposition. These data suggest that the presentation of the collagen I‐derived DGEA ligand is a feasible approach for selectively inducing an osteogenic phenotype in encapsulated MSCs. © 2015 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 103A: 3516–3525, 2015.</description><identifier>ISSN: 1549-3296</identifier><identifier>EISSN: 1552-4965</identifier><identifier>DOI: 10.1002/jbm.a.35497</identifier><identifier>PMID: 25953514</identifier><language>eng</language><publisher>United States: Blackwell Publishing Ltd</publisher><subject>alginate hydrogels ; Alginates ; Alkaline Phosphatase - metabolism ; Animals ; Biocompatibility ; Biomedical materials ; Cell adhesion ; Cell Adhesion - drug effects ; Cell Differentiation - drug effects ; Cells, Cultured ; Collagen Type I - pharmacology ; Collagens ; DGEA peptide ; Differentiation ; ECM-mimicking ligands ; Humans ; Hydrogels ; Hydrogels - pharmacology ; Ligands ; mesenchymal stem cells ; Mesenchymal Stromal Cells - cytology ; Mesenchymal Stromal Cells - drug effects ; Mice ; Oligopeptides - pharmacology ; osteogenesis ; Osteogenesis - drug effects ; Peptides - pharmacology ; Phenotype ; Rats</subject><ispartof>Journal of biomedical materials research. 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Part A</title><addtitle>J. Biomed. Mater. Res</addtitle><description>Interactions between cells and the extracellular matrix (ECM) are known to play critical roles in regulating cell phenotype. The identity of ECM ligands presented to mesenchymal stem cells (MSCs) has previously been shown to direct the cell fate commitment of these cells. To enhance osteogenic differentiation of MSCs, alginate hydrogels were prepared that present the DGEA ligand derived from collagen I. When presented from hydrogel surfaces in 2D, the DGEA ligand did not facilitate cell adhesion, while hydrogels presenting the RGD ligand derived from fibronectin did encourage cell adhesion and spreading. However, the osteogenic differentiation of MSCs encapsulated within alginate hydrogels presenting the DGEA ligand was enhanced when compared with unmodified alginate hydrogels and hydrogels presenting the RGD ligand. MSCs cultured in DGEA‐presenting gels exhibited increased levels of osteocalcin production and mineral deposition. These data suggest that the presentation of the collagen I‐derived DGEA ligand is a feasible approach for selectively inducing an osteogenic phenotype in encapsulated MSCs. © 2015 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 103A: 3516–3525, 2015.</description><subject>alginate hydrogels</subject><subject>Alginates</subject><subject>Alkaline Phosphatase - metabolism</subject><subject>Animals</subject><subject>Biocompatibility</subject><subject>Biomedical materials</subject><subject>Cell adhesion</subject><subject>Cell Adhesion - drug effects</subject><subject>Cell Differentiation - drug effects</subject><subject>Cells, Cultured</subject><subject>Collagen Type I - pharmacology</subject><subject>Collagens</subject><subject>DGEA peptide</subject><subject>Differentiation</subject><subject>ECM-mimicking ligands</subject><subject>Humans</subject><subject>Hydrogels</subject><subject>Hydrogels - pharmacology</subject><subject>Ligands</subject><subject>mesenchymal stem cells</subject><subject>Mesenchymal Stromal Cells - cytology</subject><subject>Mesenchymal Stromal Cells - drug effects</subject><subject>Mice</subject><subject>Oligopeptides - pharmacology</subject><subject>osteogenesis</subject><subject>Osteogenesis - drug effects</subject><subject>Peptides - pharmacology</subject><subject>Phenotype</subject><subject>Rats</subject><issn>1549-3296</issn><issn>1552-4965</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqN0k1v1DAQBuAIgWgpnLgjS1yQUBZ_xHZ8QVpKu7QqIEFRuVleZ7JxSeJgZyn7K_jLON12BRxQT440j19nRpNlTwmeEYzpq8tlNzMzxgsl72X7hHOaF0rw-9N3oXJGldjLHsV4mbDAnD7M9ihXnHFS7Ge_zhtA1retWUGPTlDnOhidRQMMo6sAvV0czRH0jektRGR65OMIPtnJNND7cTMAcj3qIEJvm01nWpRIhyy0bURXyaAhTMURKlQHv63kCZshrlszun6Fmk0VUmobH2cPatNGeHJzHmRfjo_OD9_lZx8XJ4fzs9xyxWQuAURNhBKmMFXFiCpYKXAlKistVDXHUBrMajBEWCxMWdESyoIRs6wnqNhB9nqbO6yXHVQ2_V4wrR6C60zYaG-c_rvSu0av_A9d8DI9JlPAi5uA4L-vIY66c3HqzPTg11ETmSbMBVfkDpRSIguuxB0oKbEsGZ86eP4PvfTr0KehTUpSTPm1erlVNvgYA9S7FgnW0_rotD7a6Ov1SfrZn1PZ2dt9SYBuwZVrYfO_LH365v38NjXfXnJpMX7uLpnwTQvJJNcXHxZafL44Jqf8q_7EfgMhHOIV</recordid><startdate>201511</startdate><enddate>201511</enddate><creator>Mehta, Manav</creator><creator>Madl, Christopher M.</creator><creator>Lee, Shimwoo</creator><creator>Duda, Georg N.</creator><creator>Mooney, David J.</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</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>7QF</scope><scope>7QO</scope><scope>7QQ</scope><scope>7SC</scope><scope>7SE</scope><scope>7SP</scope><scope>7SR</scope><scope>7TA</scope><scope>7TB</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>F28</scope><scope>FR3</scope><scope>H8D</scope><scope>H8G</scope><scope>JG9</scope><scope>JQ2</scope><scope>K9.</scope><scope>KR7</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>201511</creationdate><title>The collagen I mimetic peptide DGEA enhances an osteogenic phenotype in mesenchymal stem cells when presented from cell-encapsulating hydrogels</title><author>Mehta, Manav ; Madl, Christopher M. ; Lee, Shimwoo ; Duda, Georg N. ; Mooney, David J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5937-7ee6f1696a4add31943860d6dc7cedf50e8a03fea16c06a8d28e8431abf386093</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>alginate hydrogels</topic><topic>Alginates</topic><topic>Alkaline Phosphatase - metabolism</topic><topic>Animals</topic><topic>Biocompatibility</topic><topic>Biomedical materials</topic><topic>Cell adhesion</topic><topic>Cell Adhesion - drug effects</topic><topic>Cell Differentiation - drug effects</topic><topic>Cells, Cultured</topic><topic>Collagen Type I - pharmacology</topic><topic>Collagens</topic><topic>DGEA peptide</topic><topic>Differentiation</topic><topic>ECM-mimicking ligands</topic><topic>Humans</topic><topic>Hydrogels</topic><topic>Hydrogels - pharmacology</topic><topic>Ligands</topic><topic>mesenchymal stem cells</topic><topic>Mesenchymal Stromal Cells - cytology</topic><topic>Mesenchymal Stromal Cells - drug effects</topic><topic>Mice</topic><topic>Oligopeptides - pharmacology</topic><topic>osteogenesis</topic><topic>Osteogenesis - drug effects</topic><topic>Peptides - pharmacology</topic><topic>Phenotype</topic><topic>Rats</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mehta, Manav</creatorcontrib><creatorcontrib>Madl, Christopher M.</creatorcontrib><creatorcontrib>Lee, Shimwoo</creatorcontrib><creatorcontrib>Duda, Georg N.</creatorcontrib><creatorcontrib>Mooney, David J.</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>Aluminium Industry Abstracts</collection><collection>Biotechnology Research Abstracts</collection><collection>Ceramic Abstracts</collection><collection>Computer and Information Systems Abstracts</collection><collection>Corrosion Abstracts</collection><collection>Electronics & Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Materials Business File</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><collection>Aerospace Database</collection><collection>Copper Technical Reference Library</collection><collection>Materials Research Database</collection><collection>ProQuest Computer Science Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Civil Engineering Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Computer and Information Systems Abstracts Academic</collection><collection>Computer and Information Systems Abstracts Professional</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of biomedical materials research. Part A</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mehta, Manav</au><au>Madl, Christopher M.</au><au>Lee, Shimwoo</au><au>Duda, Georg N.</au><au>Mooney, David J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The collagen I mimetic peptide DGEA enhances an osteogenic phenotype in mesenchymal stem cells when presented from cell-encapsulating hydrogels</atitle><jtitle>Journal of biomedical materials research. Part A</jtitle><addtitle>J. Biomed. Mater. Res</addtitle><date>2015-11</date><risdate>2015</risdate><volume>103</volume><issue>11</issue><spage>3516</spage><epage>3525</epage><pages>3516-3525</pages><issn>1549-3296</issn><eissn>1552-4965</eissn><abstract>Interactions between cells and the extracellular matrix (ECM) are known to play critical roles in regulating cell phenotype. The identity of ECM ligands presented to mesenchymal stem cells (MSCs) has previously been shown to direct the cell fate commitment of these cells. To enhance osteogenic differentiation of MSCs, alginate hydrogels were prepared that present the DGEA ligand derived from collagen I. When presented from hydrogel surfaces in 2D, the DGEA ligand did not facilitate cell adhesion, while hydrogels presenting the RGD ligand derived from fibronectin did encourage cell adhesion and spreading. However, the osteogenic differentiation of MSCs encapsulated within alginate hydrogels presenting the DGEA ligand was enhanced when compared with unmodified alginate hydrogels and hydrogels presenting the RGD ligand. MSCs cultured in DGEA‐presenting gels exhibited increased levels of osteocalcin production and mineral deposition. These data suggest that the presentation of the collagen I‐derived DGEA ligand is a feasible approach for selectively inducing an osteogenic phenotype in encapsulated MSCs. © 2015 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 103A: 3516–3525, 2015.</abstract><cop>United States</cop><pub>Blackwell Publishing Ltd</pub><pmid>25953514</pmid><doi>10.1002/jbm.a.35497</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | alginate hydrogels Alginates Alkaline Phosphatase - metabolism Animals Biocompatibility Biomedical materials Cell adhesion Cell Adhesion - drug effects Cell Differentiation - drug effects Cells, Cultured Collagen Type I - pharmacology Collagens DGEA peptide Differentiation ECM-mimicking ligands Humans Hydrogels Hydrogels - pharmacology Ligands mesenchymal stem cells Mesenchymal Stromal Cells - cytology Mesenchymal Stromal Cells - drug effects Mice Oligopeptides - pharmacology osteogenesis Osteogenesis - drug effects Peptides - pharmacology Phenotype Rats |
title | The collagen I mimetic peptide DGEA enhances an osteogenic phenotype in mesenchymal stem cells when presented from cell-encapsulating hydrogels |
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