Academic Journal
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
العنوان: | 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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المؤلفون: | Hei, Wei-Hong, Almansoori, Akram A., Sung, Mi-Ae, Ju, Kyung-Won, Seo, Nari, Lee, Sung-Ho, Kim, Bong-Ju, Kim, Soung-Min, Jahng, Jeong Won, He, Hong, Lee, Jong-Ho |
المساهمون: | Kim, Soung-Min, Lee, Jong-Ho |
بيانات النشر: | Elsevier BV |
سنة النشر: | 2018 |
المجموعة: | Seoul National University: S-Space |
مصطلحات موضوعية: | PULSED ELECTROMAGNETIC-FIELD, STROMAL CELLS, SPINAL-CORD, AXONAL REGENERATION, TRANSPLANTATION, ADULT, THERAPY, Peripheral nerve regeneration, Human umbilical cord blood-derived mesenchymal stem cells, Brain-derived neurotrophic factor (BDNF) |
الوصف: | This 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. ; N ; 1 |
نوع الوثيقة: | article in journal/newspaper |
اللغة: | unknown |
تدمد: | 0304-3940 |
Relation: | Neuroscience Letters, Vol.643, pp.111-120; https://hdl.handle.net/10371/206742; 000396966100018; 2-s2.0-85013685480; 54291 |
DOI: | 10.1016/j.neulet.2017.02.030 |
الاتاحة: | https://hdl.handle.net/10371/206742 https://doi.org/10.1016/j.neulet.2017.02.030 |
رقم الانضمام: | edsbas.655B172A |
قاعدة البيانات: | BASE |
تدمد: | 03043940 |
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DOI: | 10.1016/j.neulet.2017.02.030 |