Effects of Intraperitoneal Injection of Allogeneic Bone Marrow-Derived Mesenchymal Stem Cells on Bronchiolitis Obliterans in Mice Model

dc.contributor.author Işık, Sakine
dc.contributor.author Uzuner, Nevin
dc.contributor.author Karaman, Meral
dc.contributor.author Karaman, Özkan
dc.contributor.author Kıray, Müge
dc.contributor.author Kozanoğlu, İlknur
dc.contributor.author Bağrıyanık, Hüsnü Alper
dc.contributor.author Arıkan Ayyıldız, Zeynep
dc.contributor.author Kartal Yandım, Melis
dc.contributor.author Baran, Yusuf
dc.date.accessioned 2017-10-30T12:47:24Z
dc.date.available 2017-10-30T12:47:24Z
dc.date.issued 2017
dc.description.abstract Bone marrow-derived mesenchymal stem cells (BMSCs) can ameliorate a variety of lung diseases such as asthma, lung fibrosis, and acute lung injury by its anti-inflammatory and immunmodulatory effects. In this study, we developed a mouse model of bronchiolitis obliterans (BO) and evaluated the effects of the intraperitoneal administration of BMSCs on lung histopathology and cytokine levels. 25 BALB/c mice were divided into four groups; control group (Group I), BO developed and 1x106 BMSCs-injected group (Group II), non-BO, 1x106 BMSCs-injected group (Group III), and BO developed and saline-injected group (Group IV). Histological and immunohistochemical findings of the lung tissue and the migration of BMSCs to the lung were evaluated using light and confocal microscopy techniques. Confocal microscopy evaluations showed that there was no noteworthy amount of BMSCs in the lung tissue of group III while significant amount of BMSCs was detected in group II. Wall thicknesses of terminal bronchiole and periterminal bronchiolar collagen deposition were significantly lower in group II compared to the group IV (p<0.05). Furthermore, according to the immunohistochemical staining results, CD3, CD4, CD8, CD20, CD68 and neutrophil elastase positive immune cells of group II were stained more positive than group IV cells (p<0.05). IFN-ã IL-2 and TNF-á levels in bronchoalveolar lavage fluid (BALF) were significantly lower in group II compared to group IV (p<0.05). The findings of this study indicate that intraperitoneally administered BMSCs have potent effects on histopatological changes of the lung tissue and cytokine levels in the murine model of BO. en_US
dc.description.sponsorship Scientific and Technological Council of Turkey (112S148) en_US
dc.identifier.citation Işık, S., Uzuner, N., Karaman, M., Karaman, Ö., Kıray, M., Kozanoğlu, İ., Bağrıyanık, H. A., Arıkan Ayyıldız, Z., Kartal Yandım, M., and Baran, Y. (2017). Effects of intraperitoneal injection of allogeneic bone marrow-derived mesenchymal stem cells on bronchiolitis obliterans in mice model. Iranian Journal of Allergy, Asthma and Immunology, 16(3), 205-218. en_US
dc.identifier.issn 1735-1502
dc.identifier.issn 1735-5249
dc.identifier.scopus 2-s2.0-85021061245
dc.identifier.uri https://hdl.handle.net/11147/6424
dc.language.iso en en_US
dc.publisher Tehran University of Medical Sciences en_US
dc.relation.ispartof Iranian Journal of Allergy, Asthma and Immunology en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject Bronchiolitis obliterans en_US
dc.subject Intraperitoneal administration en_US
dc.subject Mesenchymal stem cells en_US
dc.subject Murine model en_US
dc.title Effects of Intraperitoneal Injection of Allogeneic Bone Marrow-Derived Mesenchymal Stem Cells on Bronchiolitis Obliterans in Mice Model en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.institutional Kartal Yandım, Melis
gdc.author.institutional Baran, Yusuf
gdc.author.yokid 119193
gdc.bip.impulseclass C5
gdc.bip.influenceclass C5
gdc.bip.popularityclass C5
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 218 en_US
gdc.description.issue 3 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q3
gdc.description.startpage 205 en_US
gdc.description.volume 16 en_US
gdc.description.wosquality Q3
gdc.identifier.openalex W2623216608
gdc.identifier.pmid 28732434
gdc.identifier.wos WOS:000406133200005
gdc.index.type WoS
gdc.index.type Scopus
gdc.index.type PubMed
gdc.oaire.accesstype GOLD
gdc.oaire.diamondjournal false
gdc.oaire.downloads 0
gdc.oaire.impulse 1.0
gdc.oaire.influence 2.6494138E-9
gdc.oaire.isgreen true
gdc.oaire.keywords Male
gdc.oaire.keywords Gene Expression
gdc.oaire.keywords Cell Count
gdc.oaire.keywords Mesenchymal Stem Cell Transplantation
gdc.oaire.keywords Bronchiolitis obliterans
gdc.oaire.keywords Mice
gdc.oaire.keywords Genes, Reporter
gdc.oaire.keywords Intraperitoneal administration
gdc.oaire.keywords Animals
gdc.oaire.keywords Transplantation, Homologous
gdc.oaire.keywords Bronchiolitis Obliterans
gdc.oaire.keywords R
gdc.oaire.keywords Mesenchymal Stem Cells
gdc.oaire.keywords Immunohistochemistry
gdc.oaire.keywords Disease Models, Animal
gdc.oaire.keywords Treatment Outcome
gdc.oaire.keywords Mesenchymal stem cells
gdc.oaire.keywords Medicine
gdc.oaire.keywords Cytokines
gdc.oaire.keywords Murine model
gdc.oaire.keywords Biomarkers
gdc.oaire.keywords Injections, Intraperitoneal
gdc.oaire.popularity 1.1685635E-9
gdc.oaire.publicfunded false
gdc.oaire.sciencefields 0301 basic medicine
gdc.oaire.sciencefields 03 medical and health sciences
gdc.oaire.sciencefields 0303 health sciences
gdc.oaire.views 4
gdc.openalex.collaboration National
gdc.openalex.fwci 0.37680002
gdc.openalex.normalizedpercentile 0.6
gdc.opencitations.count 1
gdc.plumx.mendeley 15
gdc.plumx.pubmedcites 1
gdc.plumx.scopuscites 5
gdc.scopus.citedcount 5
gdc.wos.citedcount 5
relation.isAuthorOfPublication.latestForDiscovery 7bb863bb-9384-4a07-9fbb-b9c1ab7634a3
relation.isOrgUnitOfPublication.latestForDiscovery 9af2b05f-28ac-4013-8abe-a4dfe192da5e

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