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Adenovirus vector-mediated ex vivo gene transfer of brain-derived neurotrophic factor (BDNF) tohuman umbilical cord blood-derived mesenchymal stem cells (UCS-MSCs) promotescrush-injured rat sciatic nerve regeneration

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dc.contributor.authorHei, Wei-Hong-
dc.contributor.authorAlmansoori, Akram A.-
dc.contributor.authorSung, Mi-Ae-
dc.contributor.authorJu, Kyung-Won-
dc.contributor.authorSeo, Nari-
dc.contributor.authorLee, Sung-Ho-
dc.contributor.authorKim, Bong-Ju-
dc.contributor.authorKim, Soung-Min-
dc.contributor.authorJahng, Jeong Won-
dc.contributor.authorHe, Hong-
dc.contributor.authorLee, Jong-Ho-
dc.date.accessioned2024-08-08T01:34:39Z-
dc.date.available2024-08-08T01:34:39Z-
dc.date.created2018-09-17-
dc.date.created2018-09-17-
dc.date.issued2017-03-
dc.identifier.citationNeuroscience Letters, Vol.643, pp.111-120-
dc.identifier.issn0304-3940-
dc.identifier.urihttps://hdl.handle.net/10371/206742-
dc.description.abstractThis study was designed toinvestigate the efficacy of adenovirus vector -mediated brain -derived neurotrophic factor (BDNF) ex vivo gene transfer to human umbilical cord blood -derived mesenchymal stem cells (UCB-MSCs) in a rat sciatic nerve crush injury model. BDNF protein and mRNA expression after infection was checked through an enzyme -linked immunosorbent assay (ELISA) and quantitative real-time polymerase chain reaction (qRT-PCR). Male Sprague-Dawley rats (200-250g, 6 weeks old) were distributed into threegroups (n=20 each): the control group, UCB-MSC group, and BDNF-adenovirus infected UCB-MSC (BDNF-Ad+UCB-MSC) group. UCB-MSCs (1 x 10(6) cells/10 mu l/rat) or BDNF-Ad+UCB-MSCs (1 x 10(6) cells/10 mu l/rat)were transplantedinto the rats at the crush site immediately after sciatic nerve injury. Cell tracking was done with PKH26-labeled UCB-MSCs and BDNF-Ad + UCB-MSCs (1 x 10(6) cells/10 mu l/rat). The rats were monitored for 4 weeks post surgery. Results showed that expression of BDNF at both the protein and mRNA levels was higher inthe BDNF-Ad + UCB-MSC group compared to theUCB-MSC group in vitro.Moreover, BDNF mRNA expression was higher in both UCB-MSC group and BDNF-Ad+ UCB-MSC group compared tothe control group, and BDNF mRNA expression in theBDNF-Ad + UCB-MSC group was higher than inboth other groups 5 days after surgeryin vivo. Labeled neurons in tile dorsal root ganglia (DRG), axon counts, axon density, and sciatic function index were significantly increased in the UCB-MSC and BDNF-Ad+ UCB-MSCgroupscompared to the controlgroup four weeksaftercell transplantation. Importantly,the BDNF-Ad + UCB-MSCgroup exhibited more peripheral nerve regeneration than the other two groups.Our results indicate thatboth UCB-MSCs and BDNF-Ad + UCB-MSCscan improve rat sciatic nerve regeneration, with BDNF-Ad + UCBMSCsshowing a greater effectthan UCB-MSCs. (C) 2017 Elsevier B.V. All rights reserved.-
dc.language영어-
dc.publisherElsevier BV-
dc.titleAdenovirus vector-mediated ex vivo gene transfer of brain-derived neurotrophic factor (BDNF) tohuman umbilical cord blood-derived mesenchymal stem cells (UCS-MSCs) promotescrush-injured rat sciatic nerve regeneration-
dc.typeArticle-
dc.identifier.doi10.1016/j.neulet.2017.02.030-
dc.citation.journaltitleNeuroscience Letters-
dc.identifier.wosid000396966100018-
dc.identifier.scopusid2-s2.0-85013685480-
dc.citation.endpage120-
dc.citation.startpage111-
dc.citation.volume643-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorKim, Soung-Min-
dc.contributor.affiliatedAuthorLee, Jong-Ho-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusPULSED ELECTROMAGNETIC-FIELD-
dc.subject.keywordPlusSTROMAL CELLS-
dc.subject.keywordPlusSPINAL-CORD-
dc.subject.keywordPlusAXONAL REGENERATION-
dc.subject.keywordPlusTRANSPLANTATION-
dc.subject.keywordPlusADULT-
dc.subject.keywordPlusTHERAPY-
dc.subject.keywordAuthorPeripheral nerve regeneration-
dc.subject.keywordAuthorHuman umbilical cord blood-derived mesenchymal stem cells-
dc.subject.keywordAuthorBrain-derived neurotrophic factor (BDNF)-
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