Cryopreservation does not affect the stem characteristics of multipotent cells isolated from equine peripheral blood.
Abstract: Mammalian adult stem cells show, in vitro, extensive differentiative ability and may represent a versatile tool for tissue regenerative purposes, even after long-term storage. Multipotent stem cells isolated from horse blood have been shown to possess the capacity to differentiate into diverse mesenchymal lineages although their full characterization is still at an early stage. The aim of this study was to examine the effects of cryopreservation on stemness characteristics of adult equine mesenchymal stem cells isolated from peripheral blood (ePB-MSC). Each sample of ePB-MSC was analyzed immediately and then after being frozen in liquid nitrogen for 10-12 months. After cryopreservation, cells conserved their morphology, alkaline phosphatase positivity, telomerase activity, karyotype profile, proliferation rate, and CD expression pattern. We characterized ePB-MSC as cells expressing CD44, CD90, CD117, and CD13, but not CD34 and CD45. Finally, freezing and storing ePB-MSC did not change their adipogenic, osteogenic, and myogenic differentiative potential, as analyzed by histochemistry, immunofluorescence, and polymerase chain reaction expression analyses. Overall, our results demonstrate that cryopreservation of ePB-MSC provides a convenient tool for in vitro applications, because cryopreserved cells possess the same stem characteristics as freshly isolated cells. Moreover, the feasibility of maintaining stem cell features of ePB-MSC after long-term storage has important implications for autologous cellular-based therapy in veterinary medicine.
Publication Date: 2009-10-21 PubMed ID: 19839741DOI: 10.1089/ten.TEC.2009.0512Google Scholar: Lookup
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- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
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The research article presents a study on the impact of cryopreservation on the stem characteristics of multipotent cells isolated from equine peripheral blood. It suggests that cryopreservation does not alter the cellular properties, thus indicating its potential usefulness in both in vitro applications and cellular-based therapy.
Objective of the Study
- The primary objective of this study was to analyze the effects of cryopreservation on stemness characteristics of adult equine mesenchymal stem cells isolated from peripheral blood (ePB-MSC).
Methodology
- The study examined each sample of ePB-MSC both immediately after isolation and after being frozen in liquid nitrogen for a period between 10 and 12 months.
- Several parameters, including morphology, alkaline phosphatase positivity, telomerase activity, karyotype profile, proliferation rate, and CD expression pattern, were analyzed to understand the impact of cryopreservation.
- The cells were also characterized by their expression of CD44, CD90, CD117, and CD13, but the absence of CD34 and CD45.
Findings
- The results indicated that the cells retained all characteristics after the cryopreservation process, including their adipogenic, osteogenic, and myogenic differentiative potential as confirmed through histochemistry, immunofluorescence, and polymerase chain reaction expression analyses.
Implications
- The findings have significant implications for veterinary medicine as they suggest that ePB-MSC can be preserved effectively for long periods without compromising their stem features. This opens up possibilities for autologous cellular-based therapy using these cells.
- The study’s results also imply that cryopreserved equine cells could serve as a valuable resource for in vitro applications, due to their preservation of essential stem characteristics.
Cite This Article
APA
Martinello T, Bronzini I, Maccatrozzo L, Iacopetti I, Sampaolesi M, Mascarello F, Patruno M.
(2009).
Cryopreservation does not affect the stem characteristics of multipotent cells isolated from equine peripheral blood.
Tissue Eng Part C Methods, 16(4), 771-781.
https://doi.org/10.1089/ten.TEC.2009.0512 Publication
Researcher Affiliations
- Department of Experimental Veterinary Sciences, University of Padova, Legnaro, Italy.
MeSH Terms
- Animals
- Biomarkers / metabolism
- Blood Cells / cytology
- Cell Adhesion
- Cell Differentiation
- Cell Membrane / metabolism
- Cell Proliferation
- Cell Separation / methods
- Cell Shape
- Cryopreservation / methods
- Gene Expression Profiling
- Horses / blood
- Immunophenotyping
- Kinetics
- Multipotent Stem Cells / cytology
- Multipotent Stem Cells / metabolism
- Telomerase / metabolism
Citations
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