Balance between epithelial and stromal marker expression and distribution in primary culture model of porcine endometrium during real-time cell proliferation
Language English Country Italy Media print
Document type Journal Article
PubMed
30334400
PII: 3
Knihovny.cz E-resources
- MeSH
- Biomarkers metabolism MeSH
- Models, Biological MeSH
- Cell Differentiation MeSH
- Stromal Cells cytology metabolism MeSH
- Time Factors MeSH
- Endometrium cytology MeSH
- Epithelial Cells cytology metabolism MeSH
- Cells, Cultured MeSH
- Humans MeSH
- Models, Animal MeSH
- Swine MeSH
- Cell Proliferation * MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Biomarkers MeSH
The similarity between humans and pigs, when it comes to tissue morphology, makes Sus scrofa not only a good research model, but also a potential source of cells for tissue engineering. Cell samples obtained from the pig donor, could be influenced in vitro, in order to become a source of tissue material for xenotransplantation, reconstructive and regenerative medicine. Significant amounts of data point to especially major similarities in pig and human reproductive systems. Because of that, particular scientific focus is centered on research concerning porcine COCs, theca and granulosa cells in primary cultures. One of the aspects of the reproductive process, that is still largely undiscovered, is the interaction between preimplantation blastocyst and maternal uterine tissues. In this study, we used molecular analysis techniques, such as RT-qPCR and immunocytochemistry, to analyze the expression and distribution of cytokeratin 18 and panCytokeratins 8, 18 and 19 and vimentin in porcine luminal endometrial epithelial cells, coupled with analysis of their behavior in RTCA. The results have confirmed the presence of epithelial, as well as stromal cell markers in the cells, varying in levels at different stages of culture. They have also given insight into the modes of proliferation and differentiation of studied cells in in vitro culture, as well as providing additional proof for the possible mesenchymal transdifferentiation of epithelial cells.
Department of Anatomy Poznan University of Medical Sciences Poznan Poland
Department of Histology and Embryology Poznan University of Medical Sciences Poznan Poland
Department of Histology and Embryology Wroclaw Medical University Wroclaw
Department of Pathophysiology Poznan University of Medical Sciences Poznan Poland
Division of Anatomy and Histology University of Zielona Góra Zielona Góra Poland
Faculty of Biology and Biotechnology University of Warmia and Mazury in Olsztyn Olsztyn Poland
Veterinary Center Nicolaus Copernicus University in Torun Torun Poland