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

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