4.6 Article

Canine dental pulp and umbilical cord-derived mesenchymal stem cells as alternative sources for cell therapy in dogs

期刊

RESEARCH IN VETERINARY SCIENCE
卷 140, 期 -, 页码 117-124

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ELSEVIER SCI LTD
DOI: 10.1016/j.rvsc.2021.08.006

关键词

Canine stem cells; Isolation; Differentiation; Dog; Canine dental pulp; Canine umbilical cord

资金

  1. Fundacao Araucaria
  2. Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES)-Brazil [001]

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The study isolated, characterized, and evaluated canine dental pulp and umbilical cord tissue-derived mesenchymal stem cells, showing both sources possess MSC characteristics and can be safely used as alternative sources in cell therapy.
The use of regenerative medicine for pets has been growing in recent years, and an increasing number of studies have contributed to the widespread use of cell therapies in clinical veterinary medicine. Mesenchymal stem cells (MSCs) can be isolated from different sources such as dental pulp and umbilical cord. Aiming safety and reproducibility of cell therapy in clinical practice by using sources easily obtained that are usually discarded, this study isolated, characterized, and evaluated the proliferation and colony formation potential of canine dental pulp-derived mesenchymal stem cells (cDPSCs) and canine umbilical cord tissue (cUCSCs). Three samples from each source were collected, isolated, and cultured. MSCs were differentiated into three lineages and quantified by spectrophotometry. For immunophenotypic characterization, antibodies were used to analyze the expression of cell surface markers, and 7-AAD and Annexin-V were used to analyze cell viability and apoptosis, respectively. For the clonogenic assay, cells were cultured, the colonies were stained, and counted. For the proliferation assay, the cells were plated in flasks for three days and added EdU nucleoside. cDPSCs and cUCSCs showed plastic adherence and fibroblastic morphology after cultivation. Both sources showed differentiation potential and showed CD29 and CD44 positivity and CD14, CD45, CD34 and HLA-DR negativity, and low mortality and apoptosis rates. There was no difference in proliferation rates between sources. Overall, although cUCSCs had a higher number of colony-forming units than cDPSCs, both sources presented MSCs characteristics and can be used safely as alternative sources in cell therapy.

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