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Immunophenotypic, immunocytochemistry, ultrastructural, and cytogenetic characterization of mesenchymal stem cells from equine bone marrow

dc.contributor.authorMaia, Leandro [UNESP]
dc.contributor.authorLandim-Alvarenga, Fernanda C. [UNESP]
dc.contributor.authorMota, Ligia S. L. Silveira da [UNESP]
dc.contributor.authorGolim, Marjorie de Assis [UNESP]
dc.contributor.authorLaufer-Amorim, Reneé [UNESP]
dc.contributor.authorVita, Bruna de [UNESP]
dc.contributor.authorBarberini, Danielle Jaqueta [UNESP]
dc.contributor.authorListoni, Amanda Jeronimo [UNESP]
dc.contributor.authorMoraes, Carolina Nogueira de [UNESP]
dc.contributor.authorHeckler, Marta Cristina Thomas [UNESP]
dc.contributor.authorAmorim, Rogerio Martins [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-27T11:29:33Z
dc.date.available2014-05-27T11:29:33Z
dc.date.issued2013-06-01
dc.description.abstractThe aim of this study was to isolate, culture, and characterize mesenchymal stem cells (MSCs) from horse bone marrow (BM) using the techniques of flow cytometry, immunocytochemistry, cytogenetics, and electron microscopy. Immunophenotypic analysis revealed the presence of MSCs with high expression of the CD90 marker, lower expression of the CD44 marker, and absent expression of the CD34 marker. In assays of differentiation, the positive response to osteogenic (OST), chondrogenic (CDG), and adipogenic (ADP) differentiation signals was observed and characterized by deposition of calcium-rich extracellular matrix (OST), proteoglycans and collagen II (CDG) and intracellular deposition of fat drops (ADP). In immunocytochemical characterization, MSCs were immunopositive for CD44, vimentin, and PCNA, and they were negative for CD13. In the ultrastructural analysis of MSCs, the most outstanding characteristic was the presence of rough endoplasmic reticulum with very dilated cisterns filled with a low electrodensity material. Additionally, MSCs had normal karyotypes (2n=64) as evidenced by cytogenetic analysis, and aneuploidy in metaphase was not observed. The protocols for isolating, culturing, and characterizing equine MSCs used in this study were shown to be appropriate for the production of a cell population with a good potential for differentiation and without aneuploidy that can be used to study future cellular therapies. © 2013 Wiley Periodicals, Inc.en
dc.description.affiliationDepartment of Veterinary Clinics College of Veterinary Medicine and Animal Science São Paulo State University, Botucatu, São Paulo
dc.description.affiliationDepartment of Animal Reproduction and Veterinary Radiology College of Veterinary Medicine and Animal Science São Paulo State University, Botucatu, São Paulo
dc.description.affiliationDepartment of Genetics Bioscience Institute São Paulo State University, Botucatu, São Paulo
dc.description.affiliationHemocenter Division of Botucatu Medical School São Paulo State University, Botucatu, São Paulo
dc.description.affiliationUnespDepartment of Veterinary Clinics College of Veterinary Medicine and Animal Science São Paulo State University, Botucatu, São Paulo
dc.description.affiliationUnespDepartment of Animal Reproduction and Veterinary Radiology College of Veterinary Medicine and Animal Science São Paulo State University, Botucatu, São Paulo
dc.description.affiliationUnespDepartment of Genetics Bioscience Institute São Paulo State University, Botucatu, São Paulo
dc.description.affiliationUnespHemocenter Division of Botucatu Medical School São Paulo State University, Botucatu, São Paulo
dc.format.extent618-624
dc.identifierhttp://dx.doi.org/10.1002/jemt.22208
dc.identifier.citationMicroscopy Research and Technique, v. 76, n. 6, p. 618-624, 2013.
dc.identifier.doi10.1002/jemt.22208
dc.identifier.issn1059-910X
dc.identifier.issn1097-0029
dc.identifier.lattes8456490300814833
dc.identifier.orcid0000-0002-2420-2550
dc.identifier.scopus2-s2.0-84878189553
dc.identifier.urihttp://hdl.handle.net/11449/75471
dc.identifier.wosWOS:000319298200008
dc.language.isoeng
dc.relation.ispartofMicroscopy Research and Technique
dc.relation.ispartofjcr1.087
dc.rights.accessRightsAcesso restrito
dc.sourceScopus
dc.subjectDifferentiation
dc.subjectHorse
dc.subjectIsolation
dc.subjectMesenchymal stem cells
dc.subjectSurface marker
dc.subjectEquidae
dc.titleImmunophenotypic, immunocytochemistry, ultrastructural, and cytogenetic characterization of mesenchymal stem cells from equine bone marrowen
dc.typeArtigo
dcterms.licensehttp://olabout.wiley.com/WileyCDA/Section/id-406071.html
dspace.entity.typePublication
unesp.author.lattes8456490300814833[2]
unesp.author.orcid0000-0002-8653-7938[11]
unesp.author.orcid0000-0003-4513-753X[3]
unesp.author.orcid0000-0002-2420-2550[2]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Biociências, Botucatupt
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Medicina Veterinária e Zootecnia, Botucatupt
unesp.departmentClínica Veterinária - FMVZpt
unesp.departmentReprodução Animal e Radiologia Veterinária - FMVZpt
unesp.departmentGenética - IBBpt

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