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dc.contributor.authorSatar B.
dc.contributor.authorHidir Y.
dc.contributor.authorSerdar M.A.
dc.contributor.authorKucuktag Z.
dc.contributor.authorUral A.U.
dc.contributor.authorAvcu F.
dc.contributor.authorSafali M.
dc.date.accessioned2020-06-25T15:17:17Z
dc.date.available2020-06-25T15:17:17Z
dc.date.issued2012
dc.identifier.issn14653249
dc.identifier.urihttps://doi.org/10.3109/14653249.2011.651530
dc.identifier.urihttps://hdl.handle.net/20.500.12587/2274
dc.descriptionPubMed: 22268520en_US
dc.description.abstractBackground aims. The types of proteins released from mesenchymal stromal cells (MSC) are still unclear. Our aim was to compare apoptosis scores and the expression of myelin-associated glycoprotein (MAG), myelin basic protein (MBP), neural cell adhesion molecule (NCAM)-1,matrix metalloproteinase (MMP)-1A, tissue inhibitor of metalloproteinase (TIMP)-1, TIMP-1/MMP-1A ratio, nerve growth factor (NGF), brain-derived neurotrophic factor (BDNF), ciliary neurotrophic factor (CNTF), neurotrophin (NT)-3, NT-4, glial cell-derived neurotropic factor (GDNF), leukemia inhibitory factor (LIF), basic fibroblast growth factor (FGF)-2, insulin-like growth factor (IGF)-1, platelet-derived growth factor (PDGF)-? and transforming growth factor (TGF)-?1 in anastomosed facial nerves that had been treated with or without MSC. Methods. In seven rats, the buccal branch of the right facial nerve was transected, anastomosed and treated with MSC (anastomosed + MSC group). The left buccal branch was anastomosed only (anastomosed-only group). The left mandibular branch served as an intact nerve group. On days 1820, the distal segments of the branches were examined in terms of expression of the mentioned proteins and apoptosis scores using polymerase chain reaction (PCR) and terminal deoxynucleotidyl transferase-mediated digoxigenin-UTP nick end labeling (TUNEL) assays. Results. MSC application significantly increased CNTF, PDGF-?, LIF, TGF-?1, BDNF and NT-3 expression (P < 0.05). MAG expression slightly decreased whereas NCAM-1, MMP-1A and FGF-2 slightly increased(P > 0.05). Changes in other proteins and apoptosis scores were not significant. Conclusions. These results suggest that MSC increases expression of CNTF, PDGF-?, LIF,TGF-?1, BDNF and NT-3. MAG, NCAM-1, MMP-1A and FGF-2 expressions were slightly changed in this stage of nerve regeneration. The comparison of apoptotic activity was not conclusive. Overall, it appears that MSC might have differential effects on the mentioned tissue-related proteins and trophic/growth factors. © 2012 Informa Healthcare.en_US
dc.description.sponsorshipThe authors should thank Meral SARPER, MSc, and Pinar ELCI, MSc, from the Cancer Research Center and Medical Research Center of Gulhane Military Medical Academy for preparing stem cells. The authors are grateful to Tayfun Ide, Veterinary Surgeon, Manager of the Surgical Research Section, for providing maintenance of the animals. Conflict of interest: The authors have no conflict of interest. The authors are grateful to the Research and Development Center/Gulhane Military Medical Academy (Ankara/Turkiye) that funded the research.en_US
dc.language.isoengen_US
dc.publisherElsevier Inc.en_US
dc.relation.isversionof10.3109/14653249.2011.651530en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAxonen_US
dc.subjectGrowth factorsen_US
dc.subjectNerveen_US
dc.subjectNeurotrophic factorsen_US
dc.subjectStem cellen_US
dc.titleProtein profiling of anastomosed facial nerve treated with mesenchymal stromal cellsen_US
dc.typearticleen_US
dc.contributor.departmentKırıkkale Üniversitesien_US
dc.identifier.volume14en_US
dc.identifier.issue5en_US
dc.identifier.startpage522en_US
dc.identifier.endpage528en_US
dc.relation.journalCytotherapyen_US
dc.relation.publicationcategoryMakale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanıen_US


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