Isolation and characterization of equine peripheral blood-derived multipotent mesenchymal stromal cells

The objective of the study was to isolate, cultivate and characterize equine peripheral blood-derived multipotent mesenchymal stromal cells (PbMSCs). Peripheral blood was collected, followed by the isolation of mononuclear cells using density gradient reagents, and the cultivation of adherent cells....

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Detalles Bibliográficos
Autores: Carvalho, Armando De M. [UNESP], Yamada, Ana Lucia M. [UNESP], Martins, Juliana R.b. [UNESP], Maia, Leandro [UNESP], Golim, Marjorie A. [UNESP], Deffune, Elenice [UNESP], Hussni, Carlos Alberto [UNESP], Alves, Ana Liz Garcia [UNESP]
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2013
País:Brasil
Institución:Universidade Estadual Paulista (UNESP)
Repositorio:Repositório Institucional da UNESP
Idioma:inglés
OAI Identifier:oai:repositorio.unesp.br:11449/109869
Acceso en línea:http://dx.doi.org/10.1590/S0100-736X2013000900017
http://hdl.handle.net/11449/109869
Access Level:acceso abierto
Palabra clave:Caracterização imunofenotípica
diferenciação
células tronco mesenquimais
sangue periférico
equino
Immunophenotypic characterization
differentiation
mesenchymal stem cells
peripheral blood
equine
Descripción
Sumario:The objective of the study was to isolate, cultivate and characterize equine peripheral blood-derived multipotent mesenchymal stromal cells (PbMSCs). Peripheral blood was collected, followed by the isolation of mononuclear cells using density gradient reagents, and the cultivation of adherent cells. Monoclonal mouse anti-horse CD13, mouse anti-horse CD44, and mouse anti-rat CD90 antibodies were used for the immunophenotypic characterization of the surface of the PbMSCs. These cells were also cultured in specific media for adipogenic and chondrogenic differentiation. There was no expression of the CD13 marker, but CD44 and CD90 were expressed in all of the passages tested. After 14 days of cell differentiation into adipocytes, lipid droplets were observed upon Oil Red O (ORO) staining. Twenty-one days after chondrogenic differentiation, the cells were stained with Alcian Blue. Although the technique for the isolation of these cells requires improvement, the present study demonstrates the partial characterization of PbMSCs, classifying them as a promising type of progenitor cells for use in equine cell therapy.