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Vascular Progenitor Cells Isolated From Human Embryonic Stem Cells Give Rise to Endothelial and Smooth Muscle–Like Cells and Form Vascular Networks In Vivo
We report that human embryonic stem cells contain a population of vascular progenitor cells that have the ability to differentiate into endothelial-like and smooth muscle (SM)-like cells. Vascular progenitor cells were isolated from EBs grown in suspension for 10 days and were characterized by expre...
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Published in: | Circulation research 2007-08, Vol.101 (3), p.286-294 |
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creator | Ferreira, Lino S Gerecht, Sharon Shieh, Hester F Watson, Nicki Rupnick, Maria A Dallabrida, Susan M Vunjak-Novakovic, Gordana Langer, Robert |
description | We report that human embryonic stem cells contain a population of vascular progenitor cells that have the ability to differentiate into endothelial-like and smooth muscle (SM)-like cells. Vascular progenitor cells were isolated from EBs grown in suspension for 10 days and were characterized by expression of the endothelial/hematopoietic marker CD34 (CD34 cells). When these cells are subsequently cultured in EGM-2 (endothelial growth medium) supplemented with vascular endothelial growth factor-165 (50 ng/mL), they give rise to endothelial-like cells characterized by a cobblestone cell morphology, expression of endothelial markers (platelet endothelial cell-adhesion molecule-1, CD34, KDR/Flk-1, vascular endothelial cadherin, von Willebrand factor), incorporation of acetylated low-density lipoprotein, and formation of capillary-like structures when placed in Matrigel. In contrast, when CD34 cells are cultured in EGM-2 supplemented with platelet-derived growth factor-BB (50 ng/mL), they give rise to SM-like cells characterized by spindle-shape morphology, expression of SM cell markers (α-SM actin, SM myosin heavy chain, calponin, caldesmon, SM α-22), and the ability to contract and relax in response to common pharmacological agents such as carbachol and atropine but rarely form capillary-like structures when placed in Matrigel. Implantation studies in nude mice show that both cell types contribute to the formation of human microvasculature. Some microvessels contained mouse blood cells, which indicates functional integration with host vasculature. Therefore, the vascular progenitors isolated from human embryonic stem cells using methods established in the present study could provide a means to examine the mechanisms of endothelial and SM cell development, and they could also provide a potential source of cells for vascular tissue engineering. |
doi_str_mv | 10.1161/CIRCRESAHA.107.150201 |
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Vascular progenitor cells were isolated from EBs grown in suspension for 10 days and were characterized by expression of the endothelial/hematopoietic marker CD34 (CD34 cells). When these cells are subsequently cultured in EGM-2 (endothelial growth medium) supplemented with vascular endothelial growth factor-165 (50 ng/mL), they give rise to endothelial-like cells characterized by a cobblestone cell morphology, expression of endothelial markers (platelet endothelial cell-adhesion molecule-1, CD34, KDR/Flk-1, vascular endothelial cadherin, von Willebrand factor), incorporation of acetylated low-density lipoprotein, and formation of capillary-like structures when placed in Matrigel. In contrast, when CD34 cells are cultured in EGM-2 supplemented with platelet-derived growth factor-BB (50 ng/mL), they give rise to SM-like cells characterized by spindle-shape morphology, expression of SM cell markers (α-SM actin, SM myosin heavy chain, calponin, caldesmon, SM α-22), and the ability to contract and relax in response to common pharmacological agents such as carbachol and atropine but rarely form capillary-like structures when placed in Matrigel. Implantation studies in nude mice show that both cell types contribute to the formation of human microvasculature. Some microvessels contained mouse blood cells, which indicates functional integration with host vasculature. Therefore, the vascular progenitors isolated from human embryonic stem cells using methods established in the present study could provide a means to examine the mechanisms of endothelial and SM cell development, and they could also provide a potential source of cells for vascular tissue engineering.</description><identifier>ISSN: 0009-7330</identifier><identifier>EISSN: 1524-4571</identifier><identifier>DOI: 10.1161/CIRCRESAHA.107.150201</identifier><identifier>PMID: 17569886</identifier><identifier>CODEN: CIRUAL</identifier><language>eng</language><publisher>Hagerstown, MD: American Heart Association, Inc</publisher><subject>Animals ; Antigens, CD34 - biosynthesis ; Biological and medical sciences ; Biomarkers ; Blood Vessels - cytology ; Blood Vessels - ultrastructure ; Cattle ; Cell Differentiation - drug effects ; Cell Lineage ; Cells, Cultured - cytology ; Cells, Cultured - drug effects ; Cells, Cultured - metabolism ; Cells, Cultured - transplantation ; Collagen ; Culture Media - pharmacology ; Drug Combinations ; Embryonic Stem Cells - cytology ; Embryonic Stem Cells - drug effects ; Embryonic Stem Cells - metabolism ; Embryonic Stem Cells - transplantation ; Endothelial Cells - cytology ; Fetal Blood ; Fundamental and applied biological sciences. Psychology ; Gene Expression Profiling ; Gene Expression Regulation, Developmental ; Humans ; Injections, Subcutaneous ; Laminin ; Mice ; Mice, Nude ; Morphogenesis ; Muscle Proteins - biosynthesis ; Myocytes, Smooth Muscle - cytology ; Neovascularization, Physiologic ; Organ Specificity ; Platelet-Derived Growth Factor - pharmacology ; Proteoglycans ; Proto-Oncogene Proteins c-sis ; Tissue Engineering ; Vascular Endothelial Growth Factor A - pharmacology ; Vertebrates: cardiovascular system</subject><ispartof>Circulation research, 2007-08, Vol.101 (3), p.286-294</ispartof><rights>2007 American Heart Association, Inc.</rights><rights>2007 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c6153-819a3cd49b9a5c591c18fe8ea813d6675af71e975c91950794a640ee59fde8a03</citedby><cites>FETCH-LOGICAL-c6153-819a3cd49b9a5c591c18fe8ea813d6675af71e975c91950794a640ee59fde8a03</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=18980392$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17569886$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ferreira, Lino S</creatorcontrib><creatorcontrib>Gerecht, Sharon</creatorcontrib><creatorcontrib>Shieh, Hester F</creatorcontrib><creatorcontrib>Watson, Nicki</creatorcontrib><creatorcontrib>Rupnick, Maria A</creatorcontrib><creatorcontrib>Dallabrida, Susan M</creatorcontrib><creatorcontrib>Vunjak-Novakovic, Gordana</creatorcontrib><creatorcontrib>Langer, Robert</creatorcontrib><title>Vascular Progenitor Cells Isolated From Human Embryonic Stem Cells Give Rise to Endothelial and Smooth Muscle–Like Cells and Form Vascular Networks In Vivo</title><title>Circulation research</title><addtitle>Circ Res</addtitle><description>We report that human embryonic stem cells contain a population of vascular progenitor cells that have the ability to differentiate into endothelial-like and smooth muscle (SM)-like cells. Vascular progenitor cells were isolated from EBs grown in suspension for 10 days and were characterized by expression of the endothelial/hematopoietic marker CD34 (CD34 cells). When these cells are subsequently cultured in EGM-2 (endothelial growth medium) supplemented with vascular endothelial growth factor-165 (50 ng/mL), they give rise to endothelial-like cells characterized by a cobblestone cell morphology, expression of endothelial markers (platelet endothelial cell-adhesion molecule-1, CD34, KDR/Flk-1, vascular endothelial cadherin, von Willebrand factor), incorporation of acetylated low-density lipoprotein, and formation of capillary-like structures when placed in Matrigel. In contrast, when CD34 cells are cultured in EGM-2 supplemented with platelet-derived growth factor-BB (50 ng/mL), they give rise to SM-like cells characterized by spindle-shape morphology, expression of SM cell markers (α-SM actin, SM myosin heavy chain, calponin, caldesmon, SM α-22), and the ability to contract and relax in response to common pharmacological agents such as carbachol and atropine but rarely form capillary-like structures when placed in Matrigel. Implantation studies in nude mice show that both cell types contribute to the formation of human microvasculature. Some microvessels contained mouse blood cells, which indicates functional integration with host vasculature. Therefore, the vascular progenitors isolated from human embryonic stem cells using methods established in the present study could provide a means to examine the mechanisms of endothelial and SM cell development, and they could also provide a potential source of cells for vascular tissue engineering.</description><subject>Animals</subject><subject>Antigens, CD34 - biosynthesis</subject><subject>Biological and medical sciences</subject><subject>Biomarkers</subject><subject>Blood Vessels - cytology</subject><subject>Blood Vessels - ultrastructure</subject><subject>Cattle</subject><subject>Cell Differentiation - drug effects</subject><subject>Cell Lineage</subject><subject>Cells, Cultured - cytology</subject><subject>Cells, Cultured - drug effects</subject><subject>Cells, Cultured - metabolism</subject><subject>Cells, Cultured - transplantation</subject><subject>Collagen</subject><subject>Culture Media - pharmacology</subject><subject>Drug Combinations</subject><subject>Embryonic Stem Cells - cytology</subject><subject>Embryonic Stem Cells - drug effects</subject><subject>Embryonic Stem Cells - metabolism</subject><subject>Embryonic Stem Cells - transplantation</subject><subject>Endothelial Cells - cytology</subject><subject>Fetal Blood</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene Expression Profiling</subject><subject>Gene Expression Regulation, Developmental</subject><subject>Humans</subject><subject>Injections, Subcutaneous</subject><subject>Laminin</subject><subject>Mice</subject><subject>Mice, Nude</subject><subject>Morphogenesis</subject><subject>Muscle Proteins - biosynthesis</subject><subject>Myocytes, Smooth Muscle - cytology</subject><subject>Neovascularization, Physiologic</subject><subject>Organ Specificity</subject><subject>Platelet-Derived Growth Factor - pharmacology</subject><subject>Proteoglycans</subject><subject>Proto-Oncogene Proteins c-sis</subject><subject>Tissue Engineering</subject><subject>Vascular Endothelial Growth Factor A - pharmacology</subject><subject>Vertebrates: cardiovascular system</subject><issn>0009-7330</issn><issn>1524-4571</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNqFks-O0zAQxiMEYsvCI4B8gVuKJ45j-1hV7bZS-aMW9hq5zoSGOvFiJ1vtjXfgzMvxJHjViB45WTP-ff5G_iZJXgOdAhTwfr7ezreL3Ww1mwIVU-A0o_AkmQDP8jTnAp4mE0qpSgVj9Cp5EcJ3SiFnmXqeXIHghZKymCS_b3Uwg9WefPbuG3ZN7zyZo7WBrIOzuseKLL1ryWpodUcW7d4_uK4xZNdjO4I3zT2SbROQ9I4susr1B7SNtkR3Fdm1LtbkwxCMxT8_f22aI466x-ul8y35N8NH7E_OH6N3R26be_cyeVZrG_DVeF4nX5eLL_NVuvl0s57PNqkpgLNUgtLMVLnaK80NV2BA1ihRS2BVUQiuawGoBDcKFKdC5brIKSJXdYVSU3advDu_e-fdjwFDX7ZNMHFI3aEbQllIAJlHq_-BoISELBMR5GfQeBeCx7q8802r_UMJtHwMsLwEGFuiPAcYdW9Gg2HfYnVRjYlF4O0IxE_Ttva6M024cFJJylQWufzMnZzt0YejHU7oywNq2x_KuBmUUcjSjFJBo4KmsQOM_QURb7XG</recordid><startdate>20070803</startdate><enddate>20070803</enddate><creator>Ferreira, Lino S</creator><creator>Gerecht, Sharon</creator><creator>Shieh, Hester F</creator><creator>Watson, Nicki</creator><creator>Rupnick, Maria A</creator><creator>Dallabrida, Susan M</creator><creator>Vunjak-Novakovic, Gordana</creator><creator>Langer, Robert</creator><general>American Heart Association, Inc</general><general>Lippincott</general><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>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20070803</creationdate><title>Vascular Progenitor Cells Isolated From Human Embryonic Stem Cells Give Rise to Endothelial and Smooth Muscle–Like Cells and Form Vascular Networks In Vivo</title><author>Ferreira, Lino S ; Gerecht, Sharon ; Shieh, Hester F ; Watson, Nicki ; Rupnick, Maria A ; Dallabrida, Susan M ; Vunjak-Novakovic, Gordana ; Langer, Robert</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c6153-819a3cd49b9a5c591c18fe8ea813d6675af71e975c91950794a640ee59fde8a03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Animals</topic><topic>Antigens, CD34 - biosynthesis</topic><topic>Biological and medical sciences</topic><topic>Biomarkers</topic><topic>Blood Vessels - cytology</topic><topic>Blood Vessels - ultrastructure</topic><topic>Cattle</topic><topic>Cell Differentiation - drug effects</topic><topic>Cell Lineage</topic><topic>Cells, Cultured - cytology</topic><topic>Cells, Cultured - drug effects</topic><topic>Cells, Cultured - metabolism</topic><topic>Cells, Cultured - transplantation</topic><topic>Collagen</topic><topic>Culture Media - pharmacology</topic><topic>Drug Combinations</topic><topic>Embryonic Stem Cells - cytology</topic><topic>Embryonic Stem Cells - drug effects</topic><topic>Embryonic Stem Cells - metabolism</topic><topic>Embryonic Stem Cells - transplantation</topic><topic>Endothelial Cells - cytology</topic><topic>Fetal Blood</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gene Expression Profiling</topic><topic>Gene Expression Regulation, Developmental</topic><topic>Humans</topic><topic>Injections, Subcutaneous</topic><topic>Laminin</topic><topic>Mice</topic><topic>Mice, Nude</topic><topic>Morphogenesis</topic><topic>Muscle Proteins - biosynthesis</topic><topic>Myocytes, Smooth Muscle - cytology</topic><topic>Neovascularization, Physiologic</topic><topic>Organ Specificity</topic><topic>Platelet-Derived Growth Factor - pharmacology</topic><topic>Proteoglycans</topic><topic>Proto-Oncogene Proteins c-sis</topic><topic>Tissue Engineering</topic><topic>Vascular Endothelial Growth Factor A - pharmacology</topic><topic>Vertebrates: cardiovascular system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ferreira, Lino S</creatorcontrib><creatorcontrib>Gerecht, Sharon</creatorcontrib><creatorcontrib>Shieh, Hester F</creatorcontrib><creatorcontrib>Watson, Nicki</creatorcontrib><creatorcontrib>Rupnick, Maria A</creatorcontrib><creatorcontrib>Dallabrida, Susan M</creatorcontrib><creatorcontrib>Vunjak-Novakovic, Gordana</creatorcontrib><creatorcontrib>Langer, Robert</creatorcontrib><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>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Circulation research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ferreira, Lino S</au><au>Gerecht, Sharon</au><au>Shieh, Hester F</au><au>Watson, Nicki</au><au>Rupnick, Maria A</au><au>Dallabrida, Susan M</au><au>Vunjak-Novakovic, Gordana</au><au>Langer, Robert</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Vascular Progenitor Cells Isolated From Human Embryonic Stem Cells Give Rise to Endothelial and Smooth Muscle–Like Cells and Form Vascular Networks In Vivo</atitle><jtitle>Circulation research</jtitle><addtitle>Circ Res</addtitle><date>2007-08-03</date><risdate>2007</risdate><volume>101</volume><issue>3</issue><spage>286</spage><epage>294</epage><pages>286-294</pages><issn>0009-7330</issn><eissn>1524-4571</eissn><coden>CIRUAL</coden><abstract>We report that human embryonic stem cells contain a population of vascular progenitor cells that have the ability to differentiate into endothelial-like and smooth muscle (SM)-like cells. Vascular progenitor cells were isolated from EBs grown in suspension for 10 days and were characterized by expression of the endothelial/hematopoietic marker CD34 (CD34 cells). When these cells are subsequently cultured in EGM-2 (endothelial growth medium) supplemented with vascular endothelial growth factor-165 (50 ng/mL), they give rise to endothelial-like cells characterized by a cobblestone cell morphology, expression of endothelial markers (platelet endothelial cell-adhesion molecule-1, CD34, KDR/Flk-1, vascular endothelial cadherin, von Willebrand factor), incorporation of acetylated low-density lipoprotein, and formation of capillary-like structures when placed in Matrigel. In contrast, when CD34 cells are cultured in EGM-2 supplemented with platelet-derived growth factor-BB (50 ng/mL), they give rise to SM-like cells characterized by spindle-shape morphology, expression of SM cell markers (α-SM actin, SM myosin heavy chain, calponin, caldesmon, SM α-22), and the ability to contract and relax in response to common pharmacological agents such as carbachol and atropine but rarely form capillary-like structures when placed in Matrigel. Implantation studies in nude mice show that both cell types contribute to the formation of human microvasculature. Some microvessels contained mouse blood cells, which indicates functional integration with host vasculature. Therefore, the vascular progenitors isolated from human embryonic stem cells using methods established in the present study could provide a means to examine the mechanisms of endothelial and SM cell development, and they could also provide a potential source of cells for vascular tissue engineering.</abstract><cop>Hagerstown, MD</cop><pub>American Heart Association, Inc</pub><pmid>17569886</pmid><doi>10.1161/CIRCRESAHA.107.150201</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Antigens, CD34 - biosynthesis Biological and medical sciences Biomarkers Blood Vessels - cytology Blood Vessels - ultrastructure Cattle Cell Differentiation - drug effects Cell Lineage Cells, Cultured - cytology Cells, Cultured - drug effects Cells, Cultured - metabolism Cells, Cultured - transplantation Collagen Culture Media - pharmacology Drug Combinations Embryonic Stem Cells - cytology Embryonic Stem Cells - drug effects Embryonic Stem Cells - metabolism Embryonic Stem Cells - transplantation Endothelial Cells - cytology Fetal Blood Fundamental and applied biological sciences. Psychology Gene Expression Profiling Gene Expression Regulation, Developmental Humans Injections, Subcutaneous Laminin Mice Mice, Nude Morphogenesis Muscle Proteins - biosynthesis Myocytes, Smooth Muscle - cytology Neovascularization, Physiologic Organ Specificity Platelet-Derived Growth Factor - pharmacology Proteoglycans Proto-Oncogene Proteins c-sis Tissue Engineering Vascular Endothelial Growth Factor A - pharmacology Vertebrates: cardiovascular system |
title | Vascular Progenitor Cells Isolated From Human Embryonic Stem Cells Give Rise to Endothelial and Smooth Muscle–Like Cells and Form Vascular Networks In Vivo |
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