Mesenchymal Stem Cells Ameliorate the Histopathological Changes in a Murine Model of Chronic Asthma
| dc.contributor.author | Fırıncı, Fatih | |
| dc.contributor.author | Karaman, Meral | |
| dc.contributor.author | Baran, Yusuf | |
| dc.contributor.author | Bağrıyanık, Alper | |
| dc.contributor.author | Arıkan Ayyıldız, Zeynep | |
| dc.contributor.author | Kiray, Müge | |
| dc.contributor.author | Kozanoglu, İlknur | |
| dc.contributor.author | Yılmaz, Osman | |
| dc.contributor.author | Uzuner, Nevin | |
| dc.contributor.author | Karaman, Özkan | |
| dc.coverage.doi | 10.1016/j.intimp.2011.03.009 | |
| dc.date.accessioned | 2017-03-08T07:33:08Z | |
| dc.date.available | 2017-03-08T07:33:08Z | |
| dc.date.issued | 2011 | |
| dc.description.abstract | Asthma therapies are effective in reducing inflammation but airway remodeling is poorly responsive to these agents. New therapeutic options that have fewer side effects and reverse chronic changes in the lungs are essential.Mesenchymal stemcells (MSCs) are promising for the development of novel therapies in regenerative medicine. This study aimed to examine the efficacy of MSCs on lung histopathology in amurinemodel of chronic asthma. BALB/cmicewere divided into four groups: Group 1 (control group, n=6), Group 2 (ovalbumin induced asthma only, n=10), Group 3 (ovalbumin induced asthma + MSCs, n=10), and Group 4 (MSCs only, n=10). Histological findings (basement membrane, epithelium, subepithelial smooth muscle thickness, numbers of goblet and mast cells) of the airways and MSC migration were evaluated by light, electron, and confocal microscopes. In Group 3, all early histopathological changes except epithelial thickness and all of the chronic changes were significantly ameliorated when compared with Group 2. Evaluation with confocal microscopy showed that no noteworthyamount ofMSCswere present in the lung tissues ofGroup 4while significantamount of MSCswas detected in Group 3. SerumNO levels in Group 3, were significantly lower than Group 2. The results of this study revealed that MSCs migrated to lung tissue and ameliorated bronchial asthma in murine model. Further studies are needed to evaluate the efficacy of MSCs for the treatment of asthma. | en_US |
| dc.identifier.citation | Fırıncı, F., Karaman, M., Baran, Y., Bağrıyanık, A., Arıkan Ayyıldız, Z., Kiray, M., Kozanoğlu, İ., Yılmaz, O., Uzuner, N., and Karaman, O. (2011). Mesenchymal stem cells ameliorate the histopathological changes in a murine model of chronic asthma. International Immunopharmacology, 11(8), 1120-1126. doi:10.1016/j.intimp.2011.03.009 | en_US |
| dc.identifier.doi | 10.1016/j.intimp.2011.03.009 | en_US |
| dc.identifier.doi | 10.1016/j.intimp.2011.03.009 | |
| dc.identifier.issn | 1567-5769 | |
| dc.identifier.issn | 1567-5769 | |
| dc.identifier.scopus | 2-s2.0-84860412104 | |
| dc.identifier.uri | http://doi.org/10.1016/j.intimp.2011.03.009 | |
| dc.identifier.uri | https://hdl.handle.net/11147/5003 | |
| dc.language.iso | en | en_US |
| dc.publisher | Elsevier Ltd. | en_US |
| dc.relation.ispartof | International Immunopharmacology | en_US |
| dc.rights | info:eu-repo/semantics/openAccess | en_US |
| dc.subject | Antiinflammatory | en_US |
| dc.subject | Chronic asthma | en_US |
| dc.subject | Mesenchymal stem cells | en_US |
| dc.subject | Mice | en_US |
| dc.title | Mesenchymal Stem Cells Ameliorate the Histopathological Changes in a Murine Model of Chronic Asthma | en_US |
| dc.type | Article | en_US |
| dspace.entity.type | Publication | |
| gdc.author.institutional | Baran, Yusuf | |
| gdc.author.yokid | 119193 | |
| gdc.bip.impulseclass | C4 | |
| gdc.bip.influenceclass | C4 | |
| gdc.bip.popularityclass | C4 | |
| gdc.coar.access | open access | |
| gdc.coar.type | text::journal::journal article | |
| gdc.collaboration.industrial | false | |
| gdc.description.department | İzmir Institute of Technology. Molecular Biology and Genetics | en_US |
| gdc.description.endpage | 1126 | en_US |
| gdc.description.issue | 8 | en_US |
| gdc.description.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
| gdc.description.scopusquality | Q2 | |
| gdc.description.startpage | 1120 | en_US |
| gdc.description.volume | 11 | en_US |
| gdc.description.wosquality | Q1 | |
| gdc.identifier.openalex | W2031889217 | |
| gdc.identifier.pmid | 21439399 | |
| gdc.identifier.wos | WOS:000293723400032 | |
| gdc.index.type | WoS | |
| gdc.index.type | Scopus | |
| gdc.index.type | PubMed | |
| gdc.oaire.accesstype | BRONZE | |
| gdc.oaire.diamondjournal | false | |
| gdc.oaire.impulse | 24.0 | |
| gdc.oaire.influence | 5.146774E-9 | |
| gdc.oaire.isgreen | true | |
| gdc.oaire.keywords | Inflammation | |
| gdc.oaire.keywords | Mice, Inbred BALB C | |
| gdc.oaire.keywords | Ovalbumin | |
| gdc.oaire.keywords | Mesenchymal Stem Cells | |
| gdc.oaire.keywords | Muscle, Smooth | |
| gdc.oaire.keywords | Respiratory Mucosa | |
| gdc.oaire.keywords | Mesenchymal Stem Cell Transplantation | |
| gdc.oaire.keywords | Nitric Oxide | |
| gdc.oaire.keywords | Asthma | |
| gdc.oaire.keywords | Basement Membrane | |
| gdc.oaire.keywords | Mice | |
| gdc.oaire.keywords | Cell Movement | |
| gdc.oaire.keywords | Antiinflammatory | |
| gdc.oaire.keywords | Chronic asthma | |
| gdc.oaire.keywords | Mesenchymal stem cells | |
| gdc.oaire.keywords | Airway Remodeling | |
| gdc.oaire.keywords | Animals | |
| gdc.oaire.keywords | Female | |
| gdc.oaire.keywords | Goblet Cells | |
| gdc.oaire.keywords | Mast Cells | |
| gdc.oaire.popularity | 7.957002E-9 | |
| gdc.oaire.publicfunded | false | |
| gdc.oaire.sciencefields | 0301 basic medicine | |
| gdc.oaire.sciencefields | 0303 health sciences | |
| gdc.oaire.sciencefields | 03 medical and health sciences | |
| gdc.openalex.collaboration | National | |
| gdc.openalex.fwci | 4.14649184 | |
| gdc.openalex.normalizedpercentile | 0.93 | |
| gdc.openalex.toppercent | TOP 10% | |
| gdc.opencitations.count | 69 | |
| gdc.plumx.crossrefcites | 45 | |
| gdc.plumx.mendeley | 61 | |
| gdc.plumx.pubmedcites | 35 | |
| gdc.plumx.scopuscites | 75 | |
| gdc.scopus.citedcount | 75 | |
| gdc.wos.citedcount | 65 | |
| relation.isAuthorOfPublication.latestForDiscovery | 7bb863bb-9384-4a07-9fbb-b9c1ab7634a3 | |
| relation.isOrgUnitOfPublication.latestForDiscovery | 9af2b05f-28ac-4013-8abe-a4dfe192da5e |
