Functional small-diameter neovessels created using endothelial progenitor cells expanded ex vivo
Arterial conduits are increasingly preferred for surgical bypass because of inherent functional properties conferred by arterial endothelial cells, especially nitric oxide production in response to physiologic stimuli. Here we tested whether endothelial progenitor cells (EPCs) can replace arterial e...
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creator | Kaushal, Sunjay Amiel, Gilad E. Guleserian, Kristine J. Shapira, Oz M. Perry, Tjorvi Sutherland, Fraser W. Rabkin, Elena Moran, Adrian M. Schoen, Frederick J. Atala, Anthony Soker, Shay Bischoff, Joyce Mayer, John E. |
description | Arterial conduits are increasingly preferred for surgical bypass because of inherent functional properties conferred by arterial endothelial cells, especially nitric oxide production in response to physiologic stimuli. Here we tested whether endothelial progenitor cells (EPCs) can replace arterial endothelial cells and promote patency in tissue-engineered small-diameter blood vessels (4 mm). We isolated EPCs from peripheral blood of sheep, expanded them
ex vivo
and then seeded them on decellularized porcine iliac vessels. EPC-seeded grafts remained patent for 130 days as a carotid interposition graft in sheep, whereas non-seeded grafts occluded within 15 days. The EPC-explanted grafts exhibited contractile activity and nitric-oxide–mediated vascular relaxation that were similar to native carotid arteries. These results indicate that EPCs can function similarly to arterial endothelial cells and thereby confer longer vascular-graft survival. Due to their unique properties, EPCs might have other general applications for tissue-engineered structures and in treating vascular diseases. |
doi_str_mv | 10.1038/nm0901-1035 |
format | Article |
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ex vivo
and then seeded them on decellularized porcine iliac vessels. EPC-seeded grafts remained patent for 130 days as a carotid interposition graft in sheep, whereas non-seeded grafts occluded within 15 days. The EPC-explanted grafts exhibited contractile activity and nitric-oxide–mediated vascular relaxation that were similar to native carotid arteries. These results indicate that EPCs can function similarly to arterial endothelial cells and thereby confer longer vascular-graft survival. Due to their unique properties, EPCs might have other general applications for tissue-engineered structures and in treating vascular diseases.</description><identifier>ISSN: 1078-8956</identifier><identifier>EISSN: 1546-170X</identifier><identifier>DOI: 10.1038/nm0901-1035</identifier><identifier>PMID: 11533707</identifier><language>eng</language><publisher>New York: Nature Publishing Group US</publisher><subject>Animals ; Biomedical and Life Sciences ; Biomedicine ; Blood Vessel Prosthesis ; Blood Vessel Prosthesis Implantation ; Cancer Research ; Cells, Cultured ; Endothelium, Vascular - cytology ; Guinea Pigs ; Infectious Diseases ; Mechanical properties ; Medicine ; Metabolic Diseases ; Molecular Medicine ; Morphology ; Neurosciences ; Nitric oxide ; Publishing ; Sheep ; Stem Cells - cytology ; Thrombosis ; Vascular diseases</subject><ispartof>Nature medicine, 2001-09, Vol.7 (9), p.1035-1040</ispartof><rights>Springer Nature America, Inc. 2001</rights><rights>COPYRIGHT 2001 Nature Publishing Group</rights><rights>Copyright Nature Publishing Group Sep 2001</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c659t-1d749506968870e0808571f43d47ce296654a38e44be5cb5e2e75aa5fbf3dc3d3</citedby><cites>FETCH-LOGICAL-c659t-1d749506968870e0808571f43d47ce296654a38e44be5cb5e2e75aa5fbf3dc3d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/nm0901-1035$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/nm0901-1035$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11533707$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kaushal, Sunjay</creatorcontrib><creatorcontrib>Amiel, Gilad E.</creatorcontrib><creatorcontrib>Guleserian, Kristine J.</creatorcontrib><creatorcontrib>Shapira, Oz M.</creatorcontrib><creatorcontrib>Perry, Tjorvi</creatorcontrib><creatorcontrib>Sutherland, Fraser W.</creatorcontrib><creatorcontrib>Rabkin, Elena</creatorcontrib><creatorcontrib>Moran, Adrian M.</creatorcontrib><creatorcontrib>Schoen, Frederick J.</creatorcontrib><creatorcontrib>Atala, Anthony</creatorcontrib><creatorcontrib>Soker, Shay</creatorcontrib><creatorcontrib>Bischoff, Joyce</creatorcontrib><creatorcontrib>Mayer, John E.</creatorcontrib><title>Functional small-diameter neovessels created using endothelial progenitor cells expanded ex vivo</title><title>Nature medicine</title><addtitle>Nat Med</addtitle><addtitle>Nat Med</addtitle><description>Arterial conduits are increasingly preferred for surgical bypass because of inherent functional properties conferred by arterial endothelial cells, especially nitric oxide production in response to physiologic stimuli. Here we tested whether endothelial progenitor cells (EPCs) can replace arterial endothelial cells and promote patency in tissue-engineered small-diameter blood vessels (4 mm). We isolated EPCs from peripheral blood of sheep, expanded them
ex vivo
and then seeded them on decellularized porcine iliac vessels. EPC-seeded grafts remained patent for 130 days as a carotid interposition graft in sheep, whereas non-seeded grafts occluded within 15 days. The EPC-explanted grafts exhibited contractile activity and nitric-oxide–mediated vascular relaxation that were similar to native carotid arteries. These results indicate that EPCs can function similarly to arterial endothelial cells and thereby confer longer vascular-graft survival. Due to their unique properties, EPCs might have other general applications for tissue-engineered structures and in treating vascular diseases.</description><subject>Animals</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Blood Vessel Prosthesis</subject><subject>Blood Vessel Prosthesis Implantation</subject><subject>Cancer Research</subject><subject>Cells, Cultured</subject><subject>Endothelium, Vascular - cytology</subject><subject>Guinea Pigs</subject><subject>Infectious Diseases</subject><subject>Mechanical properties</subject><subject>Medicine</subject><subject>Metabolic Diseases</subject><subject>Molecular Medicine</subject><subject>Morphology</subject><subject>Neurosciences</subject><subject>Nitric oxide</subject><subject>Publishing</subject><subject>Sheep</subject><subject>Stem Cells - cytology</subject><subject>Thrombosis</subject><subject>Vascular diseases</subject><issn>1078-8956</issn><issn>1546-170X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqN0s1rFDEUAPBBFFurJ-8yeCiITk0mySRzLMXWQqHgF97GbPJmNiWTbJPMsv73zTILdWVBySGP5PceyeMVxWuMzjAi4qMbUYtwlWP2pDjGjDYV5ujn0xwjLirRsuaoeBHjHUKIINY-L44wZoRwxI-LX5eTU8l4J20ZR2ltpY0cIUEoHfg1xAg2liqATKDLKRo3lOC0T0uwJuesgh_AmeRDqcBmCpuVdDpb2JRrs_Yvi2e9tBFe7faT4vvlp28Xn6ub26vri_ObSjWsTRXWnLYMNW0jBEeABBKM454STbmCum0aRiURQOkCmFowqIEzKVm_6IlWRJOT4nSum190P0FM3Wji9kky_2OKHceYU4Kaf0IsCBUNrTN8-xe881PIjYpdXROcHeYZVTMapIXOuN6nIFVuCQRpvYPe5ONz3BJBkaBt9mcHfF4aRqMOJrzbS8gmwSYNcoqxu_765f_t7Y99e_qHXYK0aRm9nbazEPfh-xmq4GMM0HerYEYZfncYddsB7OYB3MYs6ze7pk2LEfSj3U1cBh9mEPOVGyA8dvVQvQf90uEi</recordid><startdate>20010901</startdate><enddate>20010901</enddate><creator>Kaushal, Sunjay</creator><creator>Amiel, Gilad E.</creator><creator>Guleserian, Kristine J.</creator><creator>Shapira, Oz M.</creator><creator>Perry, Tjorvi</creator><creator>Sutherland, Fraser W.</creator><creator>Rabkin, Elena</creator><creator>Moran, Adrian M.</creator><creator>Schoen, Frederick J.</creator><creator>Atala, Anthony</creator><creator>Soker, Shay</creator><creator>Bischoff, Joyce</creator><creator>Mayer, John E.</creator><general>Nature Publishing Group US</general><general>Nature Publishing Group</general><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>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U7</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M2P</scope><scope>M7N</scope><scope>M7P</scope><scope>MBDVC</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>RC3</scope><scope>7QO</scope><scope>7X8</scope></search><sort><creationdate>20010901</creationdate><title>Functional small-diameter neovessels created using endothelial progenitor cells expanded ex vivo</title><author>Kaushal, Sunjay ; Amiel, Gilad E. ; Guleserian, Kristine J. ; Shapira, Oz M. ; Perry, Tjorvi ; Sutherland, Fraser W. ; Rabkin, Elena ; Moran, Adrian M. ; Schoen, Frederick J. ; Atala, Anthony ; Soker, Shay ; Bischoff, Joyce ; Mayer, John E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c659t-1d749506968870e0808571f43d47ce296654a38e44be5cb5e2e75aa5fbf3dc3d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Animals</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Blood Vessel Prosthesis</topic><topic>Blood Vessel Prosthesis Implantation</topic><topic>Cancer Research</topic><topic>Cells, Cultured</topic><topic>Endothelium, Vascular - 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Academic</collection><jtitle>Nature medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kaushal, Sunjay</au><au>Amiel, Gilad E.</au><au>Guleserian, Kristine J.</au><au>Shapira, Oz M.</au><au>Perry, Tjorvi</au><au>Sutherland, Fraser W.</au><au>Rabkin, Elena</au><au>Moran, Adrian M.</au><au>Schoen, Frederick J.</au><au>Atala, Anthony</au><au>Soker, Shay</au><au>Bischoff, Joyce</au><au>Mayer, John E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Functional small-diameter neovessels created using endothelial progenitor cells expanded ex vivo</atitle><jtitle>Nature medicine</jtitle><stitle>Nat Med</stitle><addtitle>Nat Med</addtitle><date>2001-09-01</date><risdate>2001</risdate><volume>7</volume><issue>9</issue><spage>1035</spage><epage>1040</epage><pages>1035-1040</pages><issn>1078-8956</issn><eissn>1546-170X</eissn><abstract>Arterial conduits are increasingly preferred for surgical bypass because of inherent functional properties conferred by arterial endothelial cells, especially nitric oxide production in response to physiologic stimuli. Here we tested whether endothelial progenitor cells (EPCs) can replace arterial endothelial cells and promote patency in tissue-engineered small-diameter blood vessels (4 mm). We isolated EPCs from peripheral blood of sheep, expanded them
ex vivo
and then seeded them on decellularized porcine iliac vessels. EPC-seeded grafts remained patent for 130 days as a carotid interposition graft in sheep, whereas non-seeded grafts occluded within 15 days. The EPC-explanted grafts exhibited contractile activity and nitric-oxide–mediated vascular relaxation that were similar to native carotid arteries. These results indicate that EPCs can function similarly to arterial endothelial cells and thereby confer longer vascular-graft survival. Due to their unique properties, EPCs might have other general applications for tissue-engineered structures and in treating vascular diseases.</abstract><cop>New York</cop><pub>Nature Publishing Group US</pub><pmid>11533707</pmid><doi>10.1038/nm0901-1035</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Biomedical and Life Sciences Biomedicine Blood Vessel Prosthesis Blood Vessel Prosthesis Implantation Cancer Research Cells, Cultured Endothelium, Vascular - cytology Guinea Pigs Infectious Diseases Mechanical properties Medicine Metabolic Diseases Molecular Medicine Morphology Neurosciences Nitric oxide Publishing Sheep Stem Cells - cytology Thrombosis Vascular diseases |
title | Functional small-diameter neovessels created using endothelial progenitor cells expanded ex vivo |
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