Characterisation and In Vivo Safety of Canine Adipose-Derived Stem Cells

The study characterises canine adipose-derived stem cells (cASCs) in comparison to human ASCs (hASCs) and tests their safety in a canine model after intravenous administration. cASCs from two dogs were cultured under hypoxic conditions in a medium supplemented with autologous serum. They were plasti...

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Bibliographic Details
Main Authors: Bērziņš Uldis, Matise-VanHoutana Ilze, Pētersone Ilze, Dūrītis Ilmārs, Ņikuļšins Sergejs, Bogdanova-Jātniece Ance, Kālis Mārtiņš, Svirskis Šimons, Skrastiņa Dace, Ezerta Agnese, Kozlovska Tatjana
Format: Article
Language:English
Published: Sciendo 2018-06-01
Series:Proceedings of the Latvian Academy of Sciences. Section B, Natural Sciences
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Online Access:https://doi.org/10.2478/prolas-2018-0004
Description
Summary:The study characterises canine adipose-derived stem cells (cASCs) in comparison to human ASCs (hASCs) and tests their safety in a canine model after intravenous administration. cASCs from two dogs were cultured under hypoxic conditions in a medium supplemented with autologous serum. They were plastic adherent, spindle-shaped cells that expressed CD73, CD90, and CD44 but lacked CD45, CD14, HLA-DR, and CD34. cASCs differentiated toward adipogenic, osteogenic, and chondrogenic lineages, although adipogenic differentiation capacity was low. Blast transformation reaction demonstrated that these cells significantly suppress T-cell proliferation, and this ability is dose-dependent. Intravenous administration of a cell freezing medium, therapeutic dose of cASCs (2 × 106 live cells/kg), and five times higher dose of cASCs showed no significant side effects in two dogs. Microscopic tissue lesions were limited to only mild, non-specific changes. There were no signs of malignancy. The results of the study indicate that cASCs are similar to hASCs and are safe for therapeutic applications in a canine model. The proposed methodology for ASC preparation on a non-routine basis, which includes individually optimised cell culture conditions and offers risk-adapted treatment, could be used for future personalised off-the-shelf therapies, for example, in myocardial infarction or stroke.
ISSN:1407-009X