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- Title
Adipose derived mesenchymal stem cell treatment in experimental asherman syndrome induced rats.
- Authors
Çil, Nazlı; Yaka, Mutlu; Ünal, Murat Serkant; Dodurga, Yavuz; Tan, Semih; Seçme, Mücahit; Karagür, Ege Rıza; Mete, Gülçin Abban
- Abstract
Asherman syndrome (AS) occurs due to fibrosis or uterine adhesions as a result of damage to the basal layer of the endometrium. The aim of this study is investigating the effects of adipose tissue-derived mesenchymal stem cell (ADMSC) application on the expression of vascular endothelial growth factor (VEGF), insulin-like growth factor (IGF-1), miRNA-98, miRNA199a in endometrial tissue in rats with AS. Study groups were designed as, control (C), Asherman syndrome (AS), AS + oral estrogen (ASO), AS + ADMSC (ASSC), AS + oral estrogen + ADMSC (ASSCO) with 7 samples in each group. Characterization and differentiation experiments were performed in ADMSC obtained. Two weeks after the development of the AS, ADMSC therapy was applied. BrdU (5-bromo-2′-deoxyuridine) labeling was performed to show the presence of ADMSC in the tissues. Rats were sacrificed after 8 weeks and bilateral uterine horn resection was performed. Tissues were fixed in formaldehyde. After routine tissue follow-up, sections were taken and evaluated with hematoxylin eosin staining. VEGF1 and IGF1 expressions were evaluated by immunohistochemical staining and western blot analysis. Expression changes of miR-98 and miR-199a were detected by RT-PCR. Our results showed that stem cells and estrogen giving together reduced inflammation and fibrosis in the endometrium. Immunohistochemistry and western blot results suggested that this effect was achieved especially through IGF-1. In our study, decreased miR-98 and miR-199a expressions were determined in Asherman syndrome. Furthermore, no changes of miRNA expressions were observed in treatment groups.
- Subjects
STEM cell treatment; MESENCHYMAL stem cells; HISTOCHEMISTRY; SOMATOMEDIN; INVESTIGATIONAL therapies; VASCULAR endothelial growth factors; WESTERN immunoblotting
- Publication
Molecular Biology Reports, 2020, Vol 47, Issue 6, p4541
- ISSN
0301-4851
- Publication type
Article
- DOI
10.1007/s11033-020-05505-4