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Comparison of the viability and growth in stem cell culture obtained from adipose tissue (ADAS) pre and post freeze

Comparación de la viabilidad y crecimiento en cultivo de células madre adultas obtenidas de tejido adiposo pre y post congelamiento




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Artículo Original Producto de Investigación

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Ávila Portillo, L. M., Franco Ruiz, D. J., Avila García, J. P., Riveros Arocha, A. G., & Sabogal, M. (2015). Comparison of the viability and growth in stem cell culture obtained from adipose tissue (ADAS) pre and post freeze. NOVA, 13(24), 27-38. https://doi.org/10.22490/24629448.1714

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NOVA by http://www.unicolmayor.edu.co/publicaciones/index.php/nova is distributed under a license creative commons non comertial-atribution-withoutderive 4.0 international.

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Luz Mabel Ávila Portillo
    Derly Johanna Franco Ruiz
      Jenniffer Priscila Avila García
        Angela Giselle Riveros Arocha
          Mauricio Sabogal

            Objective. Comparing viability, growth in culture, phenotype and osteogenic lineage differentiation of Adipose-Derived Adult Stem Cells (ADAS) pre and post freezing. Method. Samples were obtained from adipose tissue of healthy individuals who underwent liposuction, with later enzymatic digestion with collagenase I. The stromal vascular fraction (SVF) obtained was divided equally into two fractions one of which was cryopreserved and stored at -196 °C and the other one cultivated to passage 1 (P1) before being cryopreserved. Both fractions were cryopreserved in an automated freezing chamber using two freezing solutions: (A) DMSO/Dextran40/HSA and (B) DMSO/HESSICO/HSA kept, both were kept 3 months at -196°C and thawed in PBS/HSA/HESSICO. After thawing, both were subjected to cultivation, recount, cell viability, phenotyping and osteogenic potential. Results. Cells that were frozen with cryoprotectant solution DMSO/ Dextran40/HSA and a pre-freezing culture exhibited higher viability percentages and reached 80% culture confluence in less time. Expanded samples showed no differences in the phenotype by flow cytometry and showed differentiation to osteogenic lineage.

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            1. Gimble, J.M., Guilak, F. Adipose-derived adult stem cells: Isolation, characterization, and differentiation potential. Cytotherapy. 2003; 5 (5): 362-369.
            2. Jezierska-Wozniak K, Nosarzewska D, Tutas A, Mikolajczyk A, Oklinski MK.: Use of adipose tissue as a source of mesenchymal stem cells. Postepy Hig Med Dosw (online). 2010; 27(64):326.
            3. Patricia A. Zuk et al. Human Adipose Tissue Is a Source of Multipotent Stem Cells. Molecular Biology of the Cell. 2002; 13(12):4279–4295.
            4. Pineda Molina C, Londoño Peláez C. Obtención de células madre del tejido adiposo y su potencial de diferenciación osteogénico. Rev Ing Bioméd. 2009; 3(5): 58-65.
            5. Strem BM et al. Multipotential differentiation of adipose tissue-derived stem cells. Keio J Med. 2005; 54(3):132-41.
            6. Planas Ribó, J., Coronel Gagliardi, R. Obtención y criopreservación de células madre del tejido graso mediante liposucción. Cir.plást. iberolatinoam. 2011; 37(4):319- 324.
            7. Ávila-Portillo, L. M., Madero, J. I., López, C., León, M. F., Acosta, L., Gómez, C., Delgado, L. G., Gómez, C. J., Lozano, M., Reguero, M. T. Fundamentos de Criopreservación. Revista Colombiana de Obstetricia y Ginecología.2006; 57 (4): 291-300. 8. Sreedhar Thirumala, Jeffrey M. Gimble, Ram V. Evaluation of Methylcellulose and Dimethyl Sulfoxide as the Cryoprotectants in a Serum Free Freezing Media for Cryopreservation of Adipose-Derived Adult Stem Cells. Devireddy Stem Cells Dev. 2010l; 19(4): 513–522.
            8. Rodríguez G. L. Reconstitución de productos hematopoyéticos criopreservados: control de calidad, estabilidad osmótica y lavado de DMSO. Universidad Autónoma de Barcelona. Trabajo de Tesis.
            9. Complexo Hospitalario Universitario de Santiago. Servicio de Farmacología Clínica. Expansores plasmáticos. Boletín de información terapéutica. 2002; 1:13.
            10. Lee L.Q. Pu. Cryopreservation of adipose tissue. Organogenesis. 2009; 5(3): 138-142.
            11. Dominici M, Le Blanc K, Mueller I, et al. Minimal criteria for defining multipotent mesenchymal stromal cells. The International Society for Cellular Therapy position statement. Cytotherapy. 2006; 8(4):315-317.
            12. Peng, L., Jia, Z., Yin, X., Zhang, X., Liu, Y., Chen, P., & Zhou, C. Comparative analysis of mesenchymal stem cells from bone marrow, cartilage, and adipose tissue. Stem cells and development. 2008; 17(4): 761-774.
            13. Muñoz C.M. Comparación del número viable y fenotipo de células madre mesenquimales de tejido adiposo por método de liposucción convencional y método de liposucción por ultrasonido (Vaser®). [Trabajo de grado]. Colombia (BOG): Pontificia Universidad Javeriana; 2009.
            14. García T. y Abdelnour A. Crioconservación de Ápices y semillas de cedro (Cedrela odorata L.) mediante las técnicas de vitrificación y deshidratación. Agron. Costarricense [online]. 2013;37: 113-126.
            15. Takagi H. Recent developments in cryopreservation of shoot apices of tropical species, Cryopreservation of Tropical Germplasm Current Research Progress and Application. IPGRI. Rome, Italy. 2000: 178-191, citado por García T. y Abdelnour A. Crioconservación de Ápices y semillas de cedro (Cedrela odorata L.) mediante las técnicas de vitrificación y deshidratación. Agron. Costarricense [online]. 2013;37(1):113-126.
            16. Arévalo J. y Paéz D. Cultivo de células madre mesenquimales a partir de sangre de cordón umbilical y médula ósea [Trabajo de grado]. Colombia (BOG): Pontificia Universidad Javeriana; 2007:88p.
            17. Fuentes Lacouture MF. Optimización del sistema de cultivo y caracterización de células madre mesenquimales obtenidas a partir de médula ósea humana [Trabajo de grado]. Colombia (BOG): Pontificia Universidad Javeriana; 2008. 83 p.
            18. Peter Mark, Mandy Kleinsorge, Ralf Gaebel, et al., “Human Mesenchymal Stem Cells Display Reduced Expression of CD105 after Culture in Serum-Free Medium,” Stem Cells International, 2013, Article ID 698076, 8 pages, 2013. doi:10.1155/2013/698076
            19. Linero I. M., Doncel A., Chaparro O. Proliferación y diferenciación osteogénica de células madre mesenquimales en hidrogeles de plasma sanguíneo humano. Biomédica. 2014; 34:67-78.
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            21. DOI: http://dx.doi.org/10.22490/24629448.1714
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