Human urine-derived stem cells in combination with polycaprolactone/gelatin nanofibrous membranes enhance wound healing by promoting angiogenesis
Identifieur interne : 002A19 ( Main/Exploration ); précédent : 002A18; suivant : 002A20Human urine-derived stem cells in combination with polycaprolactone/gelatin nanofibrous membranes enhance wound healing by promoting angiogenesis
Auteurs : Yinxin Fu [République populaire de Chine] ; Junjie Guan [République populaire de Chine] ; Shangchun Guo [République populaire de Chine] ; Fei Guo [République populaire de Chine] ; Xin Niu [République populaire de Chine] ; Qiang Liu [République populaire de Chine] ; Changqing Zhang [République populaire de Chine] ; Huarong Nie [République populaire de Chine] ; Yang Wang [République populaire de Chine]Source :
- Journal of Translational Medicine [ 1479-5876 ] ; 2014.
Abstract
Despite advancements in wound healing techniques and devices, new treatments are needed to improve therapeutic outcomes. This study aimed to evaluate the potential use of a new biomaterial engineered from human urine-derived stem cells (USCs) and polycaprolactone/gelatin (PCL/GT) for wound healing.
USCs were isolated from healthy individuals. To fabricate PCL/GT composite meshes, twin-nozzle electrospinning were used to spin the PCL and gelatin solutions in normal organic solvents. The morphologies and hydrophilicity properties of PCL/GT membranes were investigated. After USCs were seeded onto a PCL/GT, cell adhesion, morphology, proliferation, and cytotoxicity were examined. Then, USCs were seeded on a PCL/GT blend nanofibrous membrane and transplanted into rabbit full-thickness skin defects for wound repair. Finally, the effect of USCs condition medium on proliferation, migration, and tube formation of human umbilical vein endothelial cells (HUVECs) were performed in vitro.
USCs were successfully isolated from urine samples and expressed specific mesenchymal stem cells markers and could differentiate into osteoblasts, adipocytes, and chondrocytes. PCL/GT membrane has suitable mechanical properties similar with skin tissue and has good biocompatibility. USCs-PCL/GT significantly enhanced the healing of full-thickness skin wounds in rabbits compared to wounds treated with PCL/GT membrane alone or untreated wounds. USCs-PCL/GT-treated wounds closed much faster, with increased re-epithelialization, collagen formation, and angiogenesis. Moreover, USCs could secrete VEGF and TGF-β1, and USC-conditioned medium enhanced the migration, proliferation, and tube formation of endothelial cells.
USCs in combination with PCL/GT significantly prompted the healing of full-thickness skin wounds in rabbits. USCs based therapy provides a novel strategy for accelerating wound closure and promoting angiogenesis.
Url:
DOI: 10.1186/s12967-014-0274-2
PubMed: 25274078
PubMed Central: 4189744
Affiliations:
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LTD, Nanchang, 330006 China</nlm:aff><country xml:lang="fr">République populaire de Chine</country><wicri:regionArea>Jiangxi Origin Bio-TECH Co. LTD, Nanchang</wicri:regionArea><placeName><settlement type="city">Nanchang</settlement><region type="province">Jiangxi</region></placeName></affiliation></author><author><name sortKey="Niu, Xin" sort="Niu, Xin" uniqKey="Niu X" first="Xin" last="Niu">Xin Niu</name><affiliation wicri:level="1"><nlm:aff id="Aff1">Institute of Microsurgery on Extremities, Shanghai Jiaotong University Affiliated Sixth People’s Hospital, Shanghai, 200233 China</nlm:aff><country xml:lang="fr">République populaire de Chine</country><wicri:regionArea>Institute of Microsurgery on Extremities, Shanghai Jiaotong University Affiliated Sixth People’s Hospital, Shanghai</wicri:regionArea><wicri:noRegion>Shanghai</wicri:noRegion></affiliation></author><author><name sortKey="Liu, Qiang" sort="Liu, Qiang" uniqKey="Liu Q" first="Qiang" last="Liu">Qiang Liu</name><affiliation wicri:level="3"><nlm:aff id="Aff3">Jiangxi Origin Bio-TECH Co. LTD, Nanchang, 330006 China</nlm:aff><country xml:lang="fr">République populaire de Chine</country><wicri:regionArea>Jiangxi Origin Bio-TECH Co. LTD, Nanchang</wicri:regionArea><placeName><settlement type="city">Nanchang</settlement><region type="province">Jiangxi</region></placeName></affiliation></author><author><name sortKey="Zhang, Changqing" sort="Zhang, Changqing" uniqKey="Zhang C" first="Changqing" last="Zhang">Changqing Zhang</name><affiliation wicri:level="1"><nlm:aff id="Aff1">Institute of Microsurgery on Extremities, Shanghai Jiaotong University Affiliated Sixth People’s Hospital, Shanghai, 200233 China</nlm:aff><country xml:lang="fr">République populaire de Chine</country><wicri:regionArea>Institute of Microsurgery on Extremities, Shanghai Jiaotong University Affiliated Sixth People’s Hospital, Shanghai</wicri:regionArea><wicri:noRegion>Shanghai</wicri:noRegion></affiliation></author><author><name sortKey="Nie, Huarong" sort="Nie, Huarong" uniqKey="Nie H" first="Huarong" last="Nie">Huarong Nie</name><affiliation wicri:level="3"><nlm:aff id="Aff3">Jiangxi Origin Bio-TECH Co. LTD, Nanchang, 330006 China</nlm:aff><country xml:lang="fr">République populaire de Chine</country><wicri:regionArea>Jiangxi Origin Bio-TECH Co. LTD, Nanchang</wicri:regionArea><placeName><settlement type="city">Nanchang</settlement><region type="province">Jiangxi</region></placeName></affiliation><affiliation wicri:level="3"><nlm:aff id="Aff4">Jiangxi Chuanqi pharmaceutical Co., LTD, Nanchang, 330039 China</nlm:aff><country xml:lang="fr">République populaire de Chine</country><wicri:regionArea>Jiangxi Chuanqi pharmaceutical Co., LTD, Nanchang</wicri:regionArea><placeName><settlement type="city">Nanchang</settlement><region type="province">Jiangxi</region></placeName></affiliation></author><author><name sortKey="Wang, Yang" sort="Wang, Yang" uniqKey="Wang Y" first="Yang" last="Wang">Yang Wang</name><affiliation wicri:level="1"><nlm:aff id="Aff1">Institute of Microsurgery on Extremities, Shanghai Jiaotong University Affiliated Sixth People’s Hospital, Shanghai, 200233 China</nlm:aff><country xml:lang="fr">République populaire de Chine</country><wicri:regionArea>Institute of Microsurgery on Extremities, Shanghai Jiaotong University Affiliated Sixth People’s Hospital, Shanghai</wicri:regionArea><wicri:noRegion>Shanghai</wicri:noRegion></affiliation></author></analytic><series><title level="j">Journal of Translational Medicine</title><idno type="eISSN">1479-5876</idno><imprint><date when="2014">2014</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><sec><title>Background</title><p>Despite advancements in wound healing techniques and devices, new treatments are needed to improve therapeutic outcomes. This study aimed to evaluate the potential use of a new biomaterial engineered from human urine-derived stem cells (USCs) and polycaprolactone/gelatin (PCL/GT) for wound healing.</p></sec><sec><title>Methods</title><p>USCs were isolated from healthy individuals. To fabricate PCL/GT composite meshes, twin-nozzle electrospinning were used to spin the PCL and gelatin solutions in normal organic solvents. The morphologies and hydrophilicity properties of PCL/GT membranes were investigated. After USCs were seeded onto a PCL/GT, cell adhesion, morphology, proliferation, and cytotoxicity were examined. Then, USCs were seeded on a PCL/GT blend nanofibrous membrane and transplanted into rabbit full-thickness skin defects for wound repair. Finally, the effect of USCs condition medium on proliferation, migration, and tube formation of human umbilical vein endothelial cells (HUVECs) were performed in vitro.</p></sec><sec><title>Results</title><p>USCs were successfully isolated from urine samples and expressed specific mesenchymal stem cells markers and could differentiate into osteoblasts, adipocytes, and chondrocytes. PCL/GT membrane has suitable mechanical properties similar with skin tissue and has good biocompatibility. USCs-PCL/GT significantly enhanced the healing of full-thickness skin wounds in rabbits compared to wounds treated with PCL/GT membrane alone or untreated wounds. USCs-PCL/GT-treated wounds closed much faster, with increased re-epithelialization, collagen formation, and angiogenesis. Moreover, USCs could secrete VEGF and TGF-β1, and USC-conditioned medium enhanced the migration, proliferation, and tube formation of endothelial cells.</p></sec><sec><title>Conclusion</title><p>USCs in combination with PCL/GT significantly prompted the healing of full-thickness skin wounds in rabbits. USCs based therapy provides a novel strategy for accelerating wound closure and promoting angiogenesis.</p></sec></div></front><back><div1 type="bibliography"><listBibl><biblStruct><analytic><author><name sortKey="Moise, A" uniqKey="Moise A">A Moise</name></author><author><name sortKey="Constantinescu, I" uniqKey="Constantinescu I">I Constantinescu</name></author><author><name sortKey="Serbanescu, B" uniqKey="Serbanescu B">B Serbanescu</name></author><author><name sortKey="Gingu, Cv" uniqKey="Gingu C">CV Gingu</name></author><author><name sortKey="Zamfirescu, Dg" uniqKey="Zamfirescu D">DG Zamfirescu</name></author><author><name sortKey="Lascar, I" uniqKey="Lascar I">I Lascar</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Hautz, T" uniqKey="Hautz T">T Hautz</name></author><author><name sortKey="Zelger, B" uniqKey="Zelger B">B Zelger</name></author><author><name sortKey="Grahammer, J" uniqKey="Grahammer J">J Grahammer</name></author><author><name 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first="Qiang" last="Liu">Qiang Liu</name><name sortKey="Nie, Huarong" sort="Nie, Huarong" uniqKey="Nie H" first="Huarong" last="Nie">Huarong Nie</name><name sortKey="Nie, Huarong" sort="Nie, Huarong" uniqKey="Nie H" first="Huarong" last="Nie">Huarong Nie</name><name sortKey="Niu, Xin" sort="Niu, Xin" uniqKey="Niu X" first="Xin" last="Niu">Xin Niu</name><name sortKey="Wang, Yang" sort="Wang, Yang" uniqKey="Wang Y" first="Yang" last="Wang">Yang Wang</name><name sortKey="Zhang, Changqing" sort="Zhang, Changqing" uniqKey="Zhang C" first="Changqing" last="Zhang">Changqing Zhang</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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