Isolation and Functional Characterization of Equine Adipos Tissue Derived Mesenchymal Stem Cells

Páll, Emöke; Toma, Sergiu; Crecan, Cristian; Cenariu, Mihai; Groza, I.

doi:10.1016/j.aaspro.2016.09.083

Cited by 2 publications

(1 citation statement)

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“…Over the last few years, stem cells have come to the researchers' attention [1][2][3]. Mesenchymal stem cells are regarded as one of the most favorable cell types for regenerative medicine because of their properties and therapeutic prospects, such as differentiation potential into the various mesenchymal lineage, anti-inflammatory, modulation of immune responses, angiogenic characteristics and low immunogenicity, which makes them ideal for allogenic cell-based therapies [4][5][6][7][8][9]. Currently, MSCs are utilized to address musculoskeletal disorders in veterinary medicine [10][11][12][13][14][15].…”

Section: Introductionmentioning

confidence: 99%

How to maintain and transport equine adipose tissue for isolating mesenchymal stem cells?

et al. 2022

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Background Adipose tissue (AT) is one of the most important mesenchymal stem cell (MSC) sources because of its high quantities, availability and ease of collection. After being collected samples, they should be transported to a laboratory for stem cell (SC) isolation, culture and expansion for future clinical application. Usually, laboratories are distant from animal husbandry centers; therefore, it is necessary to provide suitable conditions for adipose tissue transportation, such that adipose-derived MSCs are minimally affected. In the current study, the impact of tissue maintenance under different conditions on MSCs derived from these tissues was evaluated. We aimed at finding suitable and practical transportation methods in which ASCs go through the slightest changes. Results In the current study, after being collected, equine AT was randomized into eight groups: four samples were maintained in stem cell culture media at 25 οC and 4 οC for 6 and 12 hrs. as transportation via SC media groups. Three samples were frozen at three different temperatures (− 20, − 75 and − 196 οC) as cryopreserved groups; these samples were defrosted 1 week after cryopreservation. Fresh and unfrozen AT was evaluated as a control group. The tissue samples were then initiated into enzymatic digestion, isolation and the culturing of SCs. Cells at passage three were used to evaluate the ability to form colonies, proliferation rate, plotting of the cell growth curve, and viability rate. All experiments were performed in triplicate. Stem cell isolation was successful in all groups, although purification of SCs from the first series of cryopreservation at − 196 οC and two series of − 20 οC was unsuccessful. There was no significant difference between the surface area of colonies in all groups except for − 20 οC. The growth rate of transportation via stem cell media at 25 οC for 6 hrs. was similar to that of the control group. MTT analysis revealed a significant difference between 25 οC 12 hrs. Group and other experimental groups except for control, 4 οC 12 hrs. and − 196 οC group. Conclusion Data have shown freezing at − 75 οC, transportation via stem cell media at 4 οC for 12 hrs. and 25 οC for 6 hrs. are acceptable tissue preservation and transportation methods due to minor effects on MSCs features.

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