Please use this identifier to cite or link to this item: https://hdl.handle.net/11147/6275
Title: Intraperitoneal mesenchymal stem cell administration ameliorates allergic rhinitis in the murine model
Authors: Işık, Sakine
Karaman, Meral
Adan, Aysun
Kıray, Müge
Bağrıyanık, Hüsnü Alper
Çağlayan Sözmen, Şule
Kozanoğlu, İlknur
Karaman, Özkan
Baran, Yusuf
Uzuner, Nevin
Adan, Aysun
Baran, Yusuf
Izmir Institute of Technology. Molecular Biology and Genetics
Keywords: Allergic rhinitis
Asthma
Intraperitoneal route
Mesenchymal stem cells
Murine model
Issue Date: Jan-2017
Publisher: Springer Verlag
Source: Işık, S., Karaman, M., Adan, A., Kıray, M., Bağrıyanık, H. A., Çağlayan Sözmen, Ş., Kozanoğlu, İ., Karaman, Ö., Baran, Y., and Uzuner, N. (2017). Intraperitoneal mesenchymal stem cell administration ameliorates allergic rhinitis in the murine model. European Archives of Oto-Rhino-Laryngology, 274(1), 197-207. doi:10.1007/s00405-016-4166-3
Abstract: Previous studies showed that bone marrow-derived mesenchymal stem cells (BMSCs) could ameliorate a variety of immune-mediated and inflammatory diseases due to their immunomodulatory and anti-inflammatory effects. In this study, we developed a mouse model of ovalbumin (OVA) induced allergic inflammation in the upper airways and evaluated the effects of the intraperitoneal administration of BMSCs on allergic inflammation. Twenty-five BALB/c mice were divided into five groups; group I (control group), group II (sensitized and challenged with OVA and treated with saline-placebo group), group III (sensitized and challenged with OVA and treated with 1 × 106 BMSCs), group IV (sensitized and challenged with OVA and treated with 2 × 106 BMSCs), and group V (sensitized and challenged with phosphate buffered saline (PBS) and treated with 1 × 106 BMSCs). Histopathological features (number of goblet cells, eosinophils and mast cells, basement membrane, epithelium thickness, and subepithelial smooth muscle thickness) of the upper and lower airways and BMSCs migration to nasal and lung tissue were evaluated using light and confocal microscopes. Levels of cytokines in the nasal lavage fluid and lung tissue supernatants were measured using enzyme-linked immunosorbent assay (ELISA). Confocal microscopic analysis showed that there was no significant amount of BMSCs in the nasal and lung tissues of group V. However, significant amount of BMSCs were observed in group III and IV. In OVA-induced AR groups (group II, III, and IV), histopathological findings of chronic asthma, such as elevated subepithelial smooth muscle thickness, epithelium thickness, and number of goblet and mast cells, were determined. Furthermore, the number of nasal goblet and eosinophil cells, histopathological findings of chronic asthma, and IL-4, IL-5, IL-13, and NO levels was significantly lower in both BMSCs-treated groups compared to the placebo group. Our findings indicated that histopathological findings of chronic asthma were also observed in mice upon AR induction. BMSCs migrated to the nasal and lung tissues following intraperitoneal delivery and ameliorated to the airway remodeling and airway inflammation both in the upper and lower airways via the inhibition of T helper (Th) 2 immune response in the murine model of AR.
URI: http://doi.org/10.1007/s00405-016-4166-3
http://hdl.handle.net/11147/6275
ISSN: 0937-4477
Appears in Collections:Molecular Biology and Genetics / Moleküler Biyoloji ve Genetik
PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

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