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Isolation of mesenchymal stem cells from equine umbilical cord blood

BACKGROUND: There are no published studies on stem cells from equine cord blood although commercial storage of equine cord blood for future autologous stem cell transplantations is available. Mesenchymal stem cells (MSC) have been isolated from fresh umbilical cord blood of humans collected non-inva...

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Autores principales: Koch, Thomas G, Heerkens, Tammy, Thomsen, Preben D, Betts, Dean H
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1904213/
https://www.ncbi.nlm.nih.gov/pubmed/17537254
http://dx.doi.org/10.1186/1472-6750-7-26
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author Koch, Thomas G
Heerkens, Tammy
Thomsen, Preben D
Betts, Dean H
author_facet Koch, Thomas G
Heerkens, Tammy
Thomsen, Preben D
Betts, Dean H
author_sort Koch, Thomas G
collection PubMed
description BACKGROUND: There are no published studies on stem cells from equine cord blood although commercial storage of equine cord blood for future autologous stem cell transplantations is available. Mesenchymal stem cells (MSC) have been isolated from fresh umbilical cord blood of humans collected non-invasively at the time of birth and from sheep cord blood collected invasively by a surgical intrauterine approach. Mesenchymal stem cells isolation percentage from frozen-thawed human cord blood is low and the future isolation percentage of MSCs from cryopreserved equine cord blood is therefore expectedly low. The hypothesis of this study was that equine MSCs could be isolated from fresh whole equine cord blood. RESULTS: Cord blood was collected from 7 foals immediately after foaling. The mononuclear cell fraction was isolated by Ficoll density centrifugation and cultured in a DMEM low glucose based media at 38.5°C in humidified atmosphere containing 5% CO(2). In 4 out of 7 samples colonies with MSC morphology were observed. Cellular morphology varied between monolayers of elongated spindle-shaped cells to layered cell clusters of cuboidal cells with shorter cytoplasmic extensions. Positive Alizarin Red and von Kossa staining as well as significant calcium deposition and alkaline phosphatase activity confirmed osteogenesis. Histology and positive Safranin O staining of matrix glycosaminoglycans illustrated chondrogenesis. Oil Red O staining of lipid droplets confirmed adipogenesis. CONCLUSION: We here report, for the first time, the isolation of mesenchymal-like stem cells from fresh equine cord blood and their differentiation into osteocytes, chondrocytes and adipocytes. This novel isolation of equine cord blood MSCs and their preliminary in vitro differentiation positions the horse as the ideal pre-clinical animal model for proof-of-principle studies of cord blood derived MSCs.
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spelling pubmed-19042132007-06-29 Isolation of mesenchymal stem cells from equine umbilical cord blood Koch, Thomas G Heerkens, Tammy Thomsen, Preben D Betts, Dean H BMC Biotechnol Research Article BACKGROUND: There are no published studies on stem cells from equine cord blood although commercial storage of equine cord blood for future autologous stem cell transplantations is available. Mesenchymal stem cells (MSC) have been isolated from fresh umbilical cord blood of humans collected non-invasively at the time of birth and from sheep cord blood collected invasively by a surgical intrauterine approach. Mesenchymal stem cells isolation percentage from frozen-thawed human cord blood is low and the future isolation percentage of MSCs from cryopreserved equine cord blood is therefore expectedly low. The hypothesis of this study was that equine MSCs could be isolated from fresh whole equine cord blood. RESULTS: Cord blood was collected from 7 foals immediately after foaling. The mononuclear cell fraction was isolated by Ficoll density centrifugation and cultured in a DMEM low glucose based media at 38.5°C in humidified atmosphere containing 5% CO(2). In 4 out of 7 samples colonies with MSC morphology were observed. Cellular morphology varied between monolayers of elongated spindle-shaped cells to layered cell clusters of cuboidal cells with shorter cytoplasmic extensions. Positive Alizarin Red and von Kossa staining as well as significant calcium deposition and alkaline phosphatase activity confirmed osteogenesis. Histology and positive Safranin O staining of matrix glycosaminoglycans illustrated chondrogenesis. Oil Red O staining of lipid droplets confirmed adipogenesis. CONCLUSION: We here report, for the first time, the isolation of mesenchymal-like stem cells from fresh equine cord blood and their differentiation into osteocytes, chondrocytes and adipocytes. This novel isolation of equine cord blood MSCs and their preliminary in vitro differentiation positions the horse as the ideal pre-clinical animal model for proof-of-principle studies of cord blood derived MSCs. BioMed Central 2007-05-30 /pmc/articles/PMC1904213/ /pubmed/17537254 http://dx.doi.org/10.1186/1472-6750-7-26 Text en Copyright © 2007 Koch et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Koch, Thomas G
Heerkens, Tammy
Thomsen, Preben D
Betts, Dean H
Isolation of mesenchymal stem cells from equine umbilical cord blood
title Isolation of mesenchymal stem cells from equine umbilical cord blood
title_full Isolation of mesenchymal stem cells from equine umbilical cord blood
title_fullStr Isolation of mesenchymal stem cells from equine umbilical cord blood
title_full_unstemmed Isolation of mesenchymal stem cells from equine umbilical cord blood
title_short Isolation of mesenchymal stem cells from equine umbilical cord blood
title_sort isolation of mesenchymal stem cells from equine umbilical cord blood
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1904213/
https://www.ncbi.nlm.nih.gov/pubmed/17537254
http://dx.doi.org/10.1186/1472-6750-7-26
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