Phenotypical and functional characteristics of mesenchymal stem cells derived from equine umbilical cord blood
Autor: | Sandeep Kumar, P. S. Yadav, Sandeep Gera, Niharika Mohanty, Pawan Kumar, Rajender Kumar, Baldev R. Gulati |
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Rok vydání: | 2014 |
Předmět: |
0301 basic medicine
medicine.diagnostic_test biology Clinical Biochemistry Mesenchymal stem cell CD44 Biomedical Engineering CD34 Bioengineering Cell Biology Umbilical cord Flow cytometry Andrology 03 medical and health sciences Haematopoiesis 030104 developmental biology Immunophenotyping medicine.anatomical_structure Immunology medicine biology.protein CD90 Original Research Biotechnology |
Zdroj: | Cytotechnology. 68:795-807 |
ISSN: | 1573-0778 0920-9069 |
DOI: | 10.1007/s10616-014-9831-z |
Popis: | Mesenchymal stem cells (MSCs) offer promise as therapeutic aid in the repair of tendon and ligament injuries in race horses. Fetal adnexa is considered as an ideal source of MSCs due to many advantages, including non-invasive nature of isolation procedures and availability of large tissue mass for harvesting the cells. However, MSCs isolated from equine fetal adnexa have not been fully characterized due to lack of species-specific markers. Therefore, this study was carried out to isolate MSCs from equine umbilical cord blood (UCB) and characterize them using cross-reactive markers. The plastic-adherent cells could be isolated from 13 out of 20 (65 %) UCB samples. The UCB derived cells proliferated till passage 20 with average cell doubling time of 46.40 ± 2.86 h. These cells expressed mesenchymal surface markers but did not express haematopoietic/leucocytic markers by RT-PCR and immunocytochemistry. The phenotypic expression of CD29, CD44, CD73 and CD90 was shown by 96.36 ± 1.28, 93.40 ± 0.70, 73.23 ± 1.29 and 46.75 ± 3.95 % cells, respectively in flow cytometry, whereas, reactivity against the haematopoietic antigens CD34 and CD45 was observed only in 2.4 ± 0.20 and 0.1 ± 0.0 % of cells, respectively. Osteogenic and chondrogenic differentiation could be achieved using established methods, whereas the optimum adipogenic differentiation was achieved after supplementing media with 15 % rabbit serum and 20 ng/ml of recombinant human insulin. In this study, we optimized methodology for isolation, cultural characterization, differentiation and immunophenotyping of MSCs from equine UCB. Protocols and markers used in this study can be employed for unequivocal characterization of equine MSCs. |
Databáze: | OpenAIRE |
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