Derivation and characterization of monkey embryonic stem cells

<p>Abstract</p> <p>Embryonic stem (ES) cell based therapy carries great potential in the treatment of neurodegenerative diseases. However, before clinical application is realized, the safety, efficacy and feasibility of this therapeutic approach must be established in animal models...

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Main Authors: Wolf Don P, Pau K-Y Francis
Format: Article
Language:English
Published: BMC 2004-06-01
Series:Reproductive Biology and Endocrinology
Online Access:http://www.rbej.com/content/2/1/41
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spelling doaj-4402d852dd5c450eb9c3788823608b2b2020-11-24T23:58:56ZengBMCReproductive Biology and Endocrinology1477-78272004-06-01214110.1186/1477-7827-2-41Derivation and characterization of monkey embryonic stem cellsWolf Don PPau K-Y Francis<p>Abstract</p> <p>Embryonic stem (ES) cell based therapy carries great potential in the treatment of neurodegenerative diseases. However, before clinical application is realized, the safety, efficacy and feasibility of this therapeutic approach must be established in animal models. The rhesus macaque is physiologically and phylogenetically similar to the human, and therefore, is a clinically relevant animal model for biomedical research, especially that focused on neurodegenerative conditions. Undifferentiated monkey ES cells can be maintained in a pluripotent state for many passages, as characterized by a collective repertoire of markers representing embryonic cell surface molecules, enzymes and transcriptional factors. They can also be differentiated into lineage-specific phenotypes of all three embryonic germ layers by epigenetic protocols. For cell-based therapy, however, the quality of ES cells and their progeny must be ensured during the process of ES cell propagation and differentiation. While only a limited number of primate ES cell lines have been studied, it is likely that substantial inter-line variability exists. This implies that diverse ES cell lines may differ in developmental stages, lineage commitment, karyotypic normalcy, gene expression, or differentiation potential. These variables, inherited genetically and/or induced epigenetically, carry obvious complications to therapeutic applications. Our laboratory has characterized and isolated rhesus monkey ES cell lines from <it>in vitro </it>produced blastocysts. All tested cell lines carry the potential to form pluripotent embryoid bodies and nestin-positive progenitor cells. These ES cell progeny can be differentiated into phenotypes representing the endodermal, mesodermal and ectodermal lineages. This review article describes the derivation of monkey ES cell lines, characterization of the undifferentiated phenotype, and their differentiation into lineage-specific, particularly neural, phenotypes. The promises and limitations of primate ES cell-based therapy are also discussed.</p> http://www.rbej.com/content/2/1/41
collection DOAJ
language English
format Article
sources DOAJ
author Wolf Don P
Pau K-Y Francis
spellingShingle Wolf Don P
Pau K-Y Francis
Derivation and characterization of monkey embryonic stem cells
Reproductive Biology and Endocrinology
author_facet Wolf Don P
Pau K-Y Francis
author_sort Wolf Don P
title Derivation and characterization of monkey embryonic stem cells
title_short Derivation and characterization of monkey embryonic stem cells
title_full Derivation and characterization of monkey embryonic stem cells
title_fullStr Derivation and characterization of monkey embryonic stem cells
title_full_unstemmed Derivation and characterization of monkey embryonic stem cells
title_sort derivation and characterization of monkey embryonic stem cells
publisher BMC
series Reproductive Biology and Endocrinology
issn 1477-7827
publishDate 2004-06-01
description <p>Abstract</p> <p>Embryonic stem (ES) cell based therapy carries great potential in the treatment of neurodegenerative diseases. However, before clinical application is realized, the safety, efficacy and feasibility of this therapeutic approach must be established in animal models. The rhesus macaque is physiologically and phylogenetically similar to the human, and therefore, is a clinically relevant animal model for biomedical research, especially that focused on neurodegenerative conditions. Undifferentiated monkey ES cells can be maintained in a pluripotent state for many passages, as characterized by a collective repertoire of markers representing embryonic cell surface molecules, enzymes and transcriptional factors. They can also be differentiated into lineage-specific phenotypes of all three embryonic germ layers by epigenetic protocols. For cell-based therapy, however, the quality of ES cells and their progeny must be ensured during the process of ES cell propagation and differentiation. While only a limited number of primate ES cell lines have been studied, it is likely that substantial inter-line variability exists. This implies that diverse ES cell lines may differ in developmental stages, lineage commitment, karyotypic normalcy, gene expression, or differentiation potential. These variables, inherited genetically and/or induced epigenetically, carry obvious complications to therapeutic applications. Our laboratory has characterized and isolated rhesus monkey ES cell lines from <it>in vitro </it>produced blastocysts. All tested cell lines carry the potential to form pluripotent embryoid bodies and nestin-positive progenitor cells. These ES cell progeny can be differentiated into phenotypes representing the endodermal, mesodermal and ectodermal lineages. This review article describes the derivation of monkey ES cell lines, characterization of the undifferentiated phenotype, and their differentiation into lineage-specific, particularly neural, phenotypes. The promises and limitations of primate ES cell-based therapy are also discussed.</p>
url http://www.rbej.com/content/2/1/41
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