Role of Endothelial Progenitor Cells in Maintaining Stemness and Enhancing Differentiation of Mesenchymal Stem Cells by Indirect Cell–Cell Interaction
A hot issue in current research regarding stem cells for regenerative medicine is the retainment of the stemness and multipotency of stem cell. Endothelial progenitor cells (EPCs) are characterized by an angiogenic switch that induces angiogenesis and further ameliorates the local microenvironment i...
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Veröffentlicht in: | Stem cells and development 2016-01, Vol.25 (2), p.123-138 |
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creator | Wen, Li Wang, Yu Wen, Ning Yuan, Gongjie Wen, Mingling Zhang, Liang Liu, Qian Liang, Yuan Cai, Chuan Chen, Xin Ding, Yin |
description | A hot issue in current research regarding stem cells for regenerative medicine is the retainment of the stemness and multipotency of stem cell. Endothelial progenitor cells (EPCs) are characterized by an angiogenic switch that induces angiogenesis and further ameliorates the local microenvironment in ischemic organs. This study investigated whether EPCs could modulate the multipotent and differential abilities of mesenchymal stem cells (MSCs) in vitro and in vivo. We established an EPC/MSC indirect Transwell coculture system and then examined the effects of EPCs on the regulation of MSC biological properties in vitro and bone formation in vivo. The in vitro studies showed that cocultured MSCs (coMSCs) display no overt changes in cell morphology but an enhanced MSC phenotype compared with monocultured MSCs (monoMSCs). Our studies regarding the cellular, molecular, and protein characteristics of coMSCs and monoMSCs demonstrated that EPCs greatly promote the proliferation and differentiation potentials of coMSCs under indirect coculture condition. The expression of the pluripotency factors OCT4, SOX2, Nanog, and Klf4 was also upregulated in coMSCs. Furthermore, coMSCs combined with fibrin glue showed improved bone regeneration when used to repair rat alveolar bone defects compared with monoMSC grafts in vivo. This study is the first to demonstrate that EPCs have dynamic roles in maintaining MSC stemness and regulating MSC differentiation potential. |
doi_str_mv | 10.1089/scd.2015.0049 |
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Endothelial progenitor cells (EPCs) are characterized by an angiogenic switch that induces angiogenesis and further ameliorates the local microenvironment in ischemic organs. This study investigated whether EPCs could modulate the multipotent and differential abilities of mesenchymal stem cells (MSCs) in vitro and in vivo. We established an EPC/MSC indirect Transwell coculture system and then examined the effects of EPCs on the regulation of MSC biological properties in vitro and bone formation in vivo. The in vitro studies showed that cocultured MSCs (coMSCs) display no overt changes in cell morphology but an enhanced MSC phenotype compared with monocultured MSCs (monoMSCs). Our studies regarding the cellular, molecular, and protein characteristics of coMSCs and monoMSCs demonstrated that EPCs greatly promote the proliferation and differentiation potentials of coMSCs under indirect coculture condition. The expression of the pluripotency factors OCT4, SOX2, Nanog, and Klf4 was also upregulated in coMSCs. Furthermore, coMSCs combined with fibrin glue showed improved bone regeneration when used to repair rat alveolar bone defects compared with monoMSC grafts in vivo. This study is the first to demonstrate that EPCs have dynamic roles in maintaining MSC stemness and regulating MSC differentiation potential.</description><identifier>ISSN: 1547-3287</identifier><identifier>EISSN: 1557-8534</identifier><identifier>DOI: 10.1089/scd.2015.0049</identifier><identifier>PMID: 26528828</identifier><language>eng</language><publisher>United States: Mary Ann Liebert, Inc</publisher><subject>Animals ; Cell Communication - physiology ; Cell Differentiation - physiology ; Cells, Cultured ; Coculture Techniques ; Endothelial Progenitor Cells - cytology ; Mesenchymal Stromal Cells - cytology ; Neovascularization, Physiologic - physiology ; Original Research Reports ; Osteogenesis - physiology ; Rats</subject><ispartof>Stem cells and development, 2016-01, Vol.25 (2), p.123-138</ispartof><rights>2016, Mary Ann Liebert, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c403t-5d539bf6f1e62f17025da317c9e963d5d6bb3ef2f52f48e229954dab1e54da253</citedby><cites>FETCH-LOGICAL-c403t-5d539bf6f1e62f17025da317c9e963d5d6bb3ef2f52f48e229954dab1e54da253</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,27928,27929</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26528828$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wen, Li</creatorcontrib><creatorcontrib>Wang, Yu</creatorcontrib><creatorcontrib>Wen, Ning</creatorcontrib><creatorcontrib>Yuan, Gongjie</creatorcontrib><creatorcontrib>Wen, Mingling</creatorcontrib><creatorcontrib>Zhang, Liang</creatorcontrib><creatorcontrib>Liu, Qian</creatorcontrib><creatorcontrib>Liang, Yuan</creatorcontrib><creatorcontrib>Cai, Chuan</creatorcontrib><creatorcontrib>Chen, Xin</creatorcontrib><creatorcontrib>Ding, Yin</creatorcontrib><title>Role of Endothelial Progenitor Cells in Maintaining Stemness and Enhancing Differentiation of Mesenchymal Stem Cells by Indirect Cell–Cell Interaction</title><title>Stem cells and development</title><addtitle>Stem Cells Dev</addtitle><description>A hot issue in current research regarding stem cells for regenerative medicine is the retainment of the stemness and multipotency of stem cell. Endothelial progenitor cells (EPCs) are characterized by an angiogenic switch that induces angiogenesis and further ameliorates the local microenvironment in ischemic organs. This study investigated whether EPCs could modulate the multipotent and differential abilities of mesenchymal stem cells (MSCs) in vitro and in vivo. We established an EPC/MSC indirect Transwell coculture system and then examined the effects of EPCs on the regulation of MSC biological properties in vitro and bone formation in vivo. The in vitro studies showed that cocultured MSCs (coMSCs) display no overt changes in cell morphology but an enhanced MSC phenotype compared with monocultured MSCs (monoMSCs). Our studies regarding the cellular, molecular, and protein characteristics of coMSCs and monoMSCs demonstrated that EPCs greatly promote the proliferation and differentiation potentials of coMSCs under indirect coculture condition. The expression of the pluripotency factors OCT4, SOX2, Nanog, and Klf4 was also upregulated in coMSCs. Furthermore, coMSCs combined with fibrin glue showed improved bone regeneration when used to repair rat alveolar bone defects compared with monoMSC grafts in vivo. This study is the first to demonstrate that EPCs have dynamic roles in maintaining MSC stemness and regulating MSC differentiation potential.</description><subject>Animals</subject><subject>Cell Communication - physiology</subject><subject>Cell Differentiation - physiology</subject><subject>Cells, Cultured</subject><subject>Coculture Techniques</subject><subject>Endothelial Progenitor Cells - cytology</subject><subject>Mesenchymal Stromal Cells - cytology</subject><subject>Neovascularization, Physiologic - physiology</subject><subject>Original Research Reports</subject><subject>Osteogenesis - physiology</subject><subject>Rats</subject><issn>1547-3287</issn><issn>1557-8534</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkb9uFDEYxC1EREKgpEUuafbiP-tdb4mOAJESESVQr7z255zRrh1sX3Fd3oEmz8eTYHMX2hTWWKPfjCwPQu8oWVEih7OkzYoRKlaEtMMLdEKF6BspePuy3tu-4Uz2x-h1Sj8JYR2T7St0zDrBpGTyBD3ehBlwsPjcm5A3MDs14-sY7sC7HCJewzwn7Dy-Us7ncpy_w7cZFg8pYeVNCW6U19X-5KyFCD47lV3wtfUKEni92S2ltaYOfdMOX3jjIuj8z_nz8LtKMTNEpWv6DTqyak7w9qCn6Mfn8-_rr83lty8X64-XjW4Jz40wgg-T7SyFjlnaEyaM4rTXAwwdN8J008TBMiuYbSUwNgyiNWqiUIUJfoo-7HvvY_i1hZTHxSVdHqM8hG0aad8R2fWDYAVt9qiOIaUIdryPblFxN1Iy1jHGMsZYxxjrGIV_f6jeTguY__TT7xeA74FqK-9nBxPE_EztX0Bimfk</recordid><startdate>20160115</startdate><enddate>20160115</enddate><creator>Wen, Li</creator><creator>Wang, Yu</creator><creator>Wen, Ning</creator><creator>Yuan, Gongjie</creator><creator>Wen, Mingling</creator><creator>Zhang, Liang</creator><creator>Liu, Qian</creator><creator>Liang, Yuan</creator><creator>Cai, Chuan</creator><creator>Chen, Xin</creator><creator>Ding, Yin</creator><general>Mary Ann Liebert, Inc</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>7X8</scope></search><sort><creationdate>20160115</creationdate><title>Role of Endothelial Progenitor Cells in Maintaining Stemness and Enhancing Differentiation of Mesenchymal Stem Cells by Indirect Cell–Cell Interaction</title><author>Wen, Li ; Wang, Yu ; Wen, Ning ; Yuan, Gongjie ; Wen, Mingling ; Zhang, Liang ; Liu, Qian ; Liang, Yuan ; Cai, Chuan ; Chen, Xin ; Ding, Yin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c403t-5d539bf6f1e62f17025da317c9e963d5d6bb3ef2f52f48e229954dab1e54da253</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Animals</topic><topic>Cell Communication - physiology</topic><topic>Cell Differentiation - physiology</topic><topic>Cells, Cultured</topic><topic>Coculture Techniques</topic><topic>Endothelial Progenitor Cells - cytology</topic><topic>Mesenchymal Stromal Cells - cytology</topic><topic>Neovascularization, Physiologic - physiology</topic><topic>Original Research Reports</topic><topic>Osteogenesis - physiology</topic><topic>Rats</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wen, Li</creatorcontrib><creatorcontrib>Wang, Yu</creatorcontrib><creatorcontrib>Wen, Ning</creatorcontrib><creatorcontrib>Yuan, Gongjie</creatorcontrib><creatorcontrib>Wen, Mingling</creatorcontrib><creatorcontrib>Zhang, Liang</creatorcontrib><creatorcontrib>Liu, Qian</creatorcontrib><creatorcontrib>Liang, Yuan</creatorcontrib><creatorcontrib>Cai, Chuan</creatorcontrib><creatorcontrib>Chen, Xin</creatorcontrib><creatorcontrib>Ding, Yin</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>Stem cells and development</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wen, Li</au><au>Wang, Yu</au><au>Wen, Ning</au><au>Yuan, Gongjie</au><au>Wen, Mingling</au><au>Zhang, Liang</au><au>Liu, Qian</au><au>Liang, Yuan</au><au>Cai, Chuan</au><au>Chen, Xin</au><au>Ding, Yin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Role of Endothelial Progenitor Cells in Maintaining Stemness and Enhancing Differentiation of Mesenchymal Stem Cells by Indirect Cell–Cell Interaction</atitle><jtitle>Stem cells and development</jtitle><addtitle>Stem Cells Dev</addtitle><date>2016-01-15</date><risdate>2016</risdate><volume>25</volume><issue>2</issue><spage>123</spage><epage>138</epage><pages>123-138</pages><issn>1547-3287</issn><eissn>1557-8534</eissn><abstract>A hot issue in current research regarding stem cells for regenerative medicine is the retainment of the stemness and multipotency of stem cell. Endothelial progenitor cells (EPCs) are characterized by an angiogenic switch that induces angiogenesis and further ameliorates the local microenvironment in ischemic organs. This study investigated whether EPCs could modulate the multipotent and differential abilities of mesenchymal stem cells (MSCs) in vitro and in vivo. We established an EPC/MSC indirect Transwell coculture system and then examined the effects of EPCs on the regulation of MSC biological properties in vitro and bone formation in vivo. The in vitro studies showed that cocultured MSCs (coMSCs) display no overt changes in cell morphology but an enhanced MSC phenotype compared with monocultured MSCs (monoMSCs). Our studies regarding the cellular, molecular, and protein characteristics of coMSCs and monoMSCs demonstrated that EPCs greatly promote the proliferation and differentiation potentials of coMSCs under indirect coculture condition. The expression of the pluripotency factors OCT4, SOX2, Nanog, and Klf4 was also upregulated in coMSCs. Furthermore, coMSCs combined with fibrin glue showed improved bone regeneration when used to repair rat alveolar bone defects compared with monoMSC grafts in vivo. This study is the first to demonstrate that EPCs have dynamic roles in maintaining MSC stemness and regulating MSC differentiation potential.</abstract><cop>United States</cop><pub>Mary Ann Liebert, Inc</pub><pmid>26528828</pmid><doi>10.1089/scd.2015.0049</doi><tpages>16</tpages></addata></record> |
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subjects | Animals Cell Communication - physiology Cell Differentiation - physiology Cells, Cultured Coculture Techniques Endothelial Progenitor Cells - cytology Mesenchymal Stromal Cells - cytology Neovascularization, Physiologic - physiology Original Research Reports Osteogenesis - physiology Rats |
title | Role of Endothelial Progenitor Cells in Maintaining Stemness and Enhancing Differentiation of Mesenchymal Stem Cells by Indirect Cell–Cell Interaction |
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