Potential of mesenchymal stem cells for bioengineered blood vessels in comparison with other eligible cell sources
Application of stem cells in tissue engineering has proved to be effective in many cases due to great proliferation and differentiation potentials as well as possible paracrine effects of these cells. Human mesenchymal stem cells (MSCs) are recognized as a valuable source for vascular tissue enginee...
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Veröffentlicht in: | Cell and tissue research 2020-04, Vol.380 (1), p.1-13 |
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description | Application of stem cells in tissue engineering has proved to be effective in many cases due to great proliferation and differentiation potentials as well as possible paracrine effects of these cells. Human mesenchymal stem cells (MSCs) are recognized as a valuable source for vascular tissue engineering, which requires endothelial and perivascular cells. The goal of this review is to survey the potential of MSCs for engineering functional blood vessels in comparison with other cell types including bone marrow mononuclear cells, endothelial precursor cells, differentiated adult autologous smooth muscle cells, autologous endothelial cells, embryonic stem cells, and induced pluripotent stem cells. In conclusion, MSCs represent a preference in making autologous tissue-engineered vascular grafts (TEVGs) as well as off-the-shelf TEVGs for emergency vascular surgery cases. |
doi_str_mv | 10.1007/s00441-019-03161-0 |
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Human mesenchymal stem cells (MSCs) are recognized as a valuable source for vascular tissue engineering, which requires endothelial and perivascular cells. The goal of this review is to survey the potential of MSCs for engineering functional blood vessels in comparison with other cell types including bone marrow mononuclear cells, endothelial precursor cells, differentiated adult autologous smooth muscle cells, autologous endothelial cells, embryonic stem cells, and induced pluripotent stem cells. 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All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c473t-9480e7c667c33b91f8b81bf6c380923d44a3a77dcd32de2adb745ec4336aee9b3</citedby><cites>FETCH-LOGICAL-c473t-9480e7c667c33b91f8b81bf6c380923d44a3a77dcd32de2adb745ec4336aee9b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00441-019-03161-0$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00441-019-03161-0$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27923,27924,41487,42556,51318</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31897835$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Afra, Simindokht</creatorcontrib><creatorcontrib>Matin, Maryam M.</creatorcontrib><title>Potential of mesenchymal stem cells for bioengineered blood vessels in comparison with other eligible cell sources</title><title>Cell and tissue research</title><addtitle>Cell Tissue Res</addtitle><addtitle>Cell Tissue Res</addtitle><description>Application of stem cells in tissue engineering has proved to be effective in many cases due to great proliferation and differentiation potentials as well as possible paracrine effects of these cells. Human mesenchymal stem cells (MSCs) are recognized as a valuable source for vascular tissue engineering, which requires endothelial and perivascular cells. The goal of this review is to survey the potential of MSCs for engineering functional blood vessels in comparison with other cell types including bone marrow mononuclear cells, endothelial precursor cells, differentiated adult autologous smooth muscle cells, autologous endothelial cells, embryonic stem cells, and induced pluripotent stem cells. In conclusion, MSCs represent a preference in making autologous tissue-engineered vascular grafts (TEVGs) as well as off-the-shelf TEVGs for emergency vascular surgery cases.</description><subject>Analysis</subject><subject>Autografts</subject><subject>B cells</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Blood vessels</subject><subject>Bone marrow</subject><subject>Cell differentiation</subject><subject>Embryo cells</subject><subject>Embryonic stem cells</subject><subject>Endothelial cells</subject><subject>Endothelium</subject><subject>Human Genetics</subject><subject>Leukocytes (mononuclear)</subject><subject>Mesenchymal stem cells</subject><subject>Molecular Medicine</subject><subject>Paracrine signalling</subject><subject>Pluripotency</subject><subject>Proteomics</subject><subject>Review</subject><subject>Smooth muscle</subject><subject>Stem cells</subject><subject>Surgery</subject><subject>Surveys</subject><subject>Tissue engineering</subject><issn>0302-766X</issn><issn>1432-0878</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kl1rFTEQhoMo9nj0D3ghAUG82ZpsssnuZSl-QUEvFLwL2ezs2ZRscszsVvrvzemp1opIQr7mmZeZ8BLynLNTzph-g4xJySvGu4oJrsrpAdlwKeqKtbp9SDZMsLrSSn07IU8QLxnjUqnuMTkRvO10K5oNyZ_TAnHxNtA00hkQopuu53LFBWbqIASkY8q09wnizkeADAPtQ0oDvQJEKHEfqUvz3maPKdIffploWibIFILf-T7AjQ7FtGYH-JQ8Gm1AeHa7b8nXd2-_nH-oLj69_3h-dlE5qcVSdbJloJ1S2gnRd3xs-5b3o3KiZV0tBimtsFoPbhD1ALUdei0bcFIIZQG6XmzJ66PuPqfvK-BiZo-HQmyEtKKpRUFZo7ko6Mu_0MtSayzVFUqr8lkNV3fUzgYwPo5pydYdRM2Z4lqWqZpCnf6DKmOA2bsUYfTl_V7Cqz8SJrBhmTCFdfEp4n2wPoIuJ8QMo9lnP9t8bTgzB0eYoyNMcYS5cURZt-TFbWtrP8PwO-WXBQogjgCWUNxBvuv9P7I_Ae_UwCM</recordid><startdate>20200401</startdate><enddate>20200401</enddate><creator>Afra, Simindokht</creator><creator>Matin, Maryam M.</creator><general>Springer Berlin Heidelberg</general><general>Springer</general><general>Springer Nature B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QP</scope><scope>7QR</scope><scope>7RV</scope><scope>7SS</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20200401</creationdate><title>Potential of mesenchymal stem cells for bioengineered blood vessels in comparison with other eligible cell sources</title><author>Afra, Simindokht ; 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subjects | Analysis Autografts B cells Biomedical and Life Sciences Biomedicine Blood vessels Bone marrow Cell differentiation Embryo cells Embryonic stem cells Endothelial cells Endothelium Human Genetics Leukocytes (mononuclear) Mesenchymal stem cells Molecular Medicine Paracrine signalling Pluripotency Proteomics Review Smooth muscle Stem cells Surgery Surveys Tissue engineering |
title | Potential of mesenchymal stem cells for bioengineered blood vessels in comparison with other eligible cell sources |
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