Cargando…

Establishment of a translational endothelial cell model using directed differentiation of induced pluripotent stem cells from Cynomolgus monkey

Due to their broad differentiation potential, pluripotent stem cells (PSCs) offer a promising approach for generating relevant cellular models for various applications. While human PSC-based cellular models are already advanced, similar systems for non-human primates (NHPs) are still lacking. Howeve...

Descripción completa

Detalles Bibliográficos
Autores principales: Thoma, Eva C., Heckel, Tobias, Keller, David, Giroud, Nicolas, Leonard, Brian, Christensen, Klaus, Roth, Adrian, Bertinetti-Lapatki, Cristina, Graf, Martin, Patsch, Christoph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5078800/
https://www.ncbi.nlm.nih.gov/pubmed/27779219
http://dx.doi.org/10.1038/srep35830
_version_ 1782462452696350720
author Thoma, Eva C.
Heckel, Tobias
Keller, David
Giroud, Nicolas
Leonard, Brian
Christensen, Klaus
Roth, Adrian
Bertinetti-Lapatki, Cristina
Graf, Martin
Patsch, Christoph
author_facet Thoma, Eva C.
Heckel, Tobias
Keller, David
Giroud, Nicolas
Leonard, Brian
Christensen, Klaus
Roth, Adrian
Bertinetti-Lapatki, Cristina
Graf, Martin
Patsch, Christoph
author_sort Thoma, Eva C.
collection PubMed
description Due to their broad differentiation potential, pluripotent stem cells (PSCs) offer a promising approach for generating relevant cellular models for various applications. While human PSC-based cellular models are already advanced, similar systems for non-human primates (NHPs) are still lacking. However, as NHPs are the most appropriate animals for evaluating the safety of many novel pharmaceuticals, the availability of in vitro systems would be extremely useful to bridge the gap between cellular and animal models. Here, we present a NHP in vitro endothelial cell system using induced pluripotent stem cells (IPSCs) from Cynomolgus monkey (Macaca fascicularis). Based on an adapted protocol for human IPSCs, we directly differentiated macaque IPSCs into endothelial cells under chemically defined conditions. The resulting endothelial cells can be enriched using immuno-magnetic cell sorting and display endothelial marker expression and function. RNA sequencing revealed that the differentiation process closely resembled vasculogenesis. Moreover, we showed that endothelial cells derived from macaque and human IPSCs are highly similar with respect to gene expression patterns and key endothelial functions, such as inflammatory responses. These data demonstrate the power of IPSC differentiation technology to generate defined cell types for use as translational in vitro models to compare cell type-specific responses across species.
format Online
Article
Text
id pubmed-5078800
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-50788002016-10-31 Establishment of a translational endothelial cell model using directed differentiation of induced pluripotent stem cells from Cynomolgus monkey Thoma, Eva C. Heckel, Tobias Keller, David Giroud, Nicolas Leonard, Brian Christensen, Klaus Roth, Adrian Bertinetti-Lapatki, Cristina Graf, Martin Patsch, Christoph Sci Rep Article Due to their broad differentiation potential, pluripotent stem cells (PSCs) offer a promising approach for generating relevant cellular models for various applications. While human PSC-based cellular models are already advanced, similar systems for non-human primates (NHPs) are still lacking. However, as NHPs are the most appropriate animals for evaluating the safety of many novel pharmaceuticals, the availability of in vitro systems would be extremely useful to bridge the gap between cellular and animal models. Here, we present a NHP in vitro endothelial cell system using induced pluripotent stem cells (IPSCs) from Cynomolgus monkey (Macaca fascicularis). Based on an adapted protocol for human IPSCs, we directly differentiated macaque IPSCs into endothelial cells under chemically defined conditions. The resulting endothelial cells can be enriched using immuno-magnetic cell sorting and display endothelial marker expression and function. RNA sequencing revealed that the differentiation process closely resembled vasculogenesis. Moreover, we showed that endothelial cells derived from macaque and human IPSCs are highly similar with respect to gene expression patterns and key endothelial functions, such as inflammatory responses. These data demonstrate the power of IPSC differentiation technology to generate defined cell types for use as translational in vitro models to compare cell type-specific responses across species. Nature Publishing Group 2016-10-25 /pmc/articles/PMC5078800/ /pubmed/27779219 http://dx.doi.org/10.1038/srep35830 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Thoma, Eva C.
Heckel, Tobias
Keller, David
Giroud, Nicolas
Leonard, Brian
Christensen, Klaus
Roth, Adrian
Bertinetti-Lapatki, Cristina
Graf, Martin
Patsch, Christoph
Establishment of a translational endothelial cell model using directed differentiation of induced pluripotent stem cells from Cynomolgus monkey
title Establishment of a translational endothelial cell model using directed differentiation of induced pluripotent stem cells from Cynomolgus monkey
title_full Establishment of a translational endothelial cell model using directed differentiation of induced pluripotent stem cells from Cynomolgus monkey
title_fullStr Establishment of a translational endothelial cell model using directed differentiation of induced pluripotent stem cells from Cynomolgus monkey
title_full_unstemmed Establishment of a translational endothelial cell model using directed differentiation of induced pluripotent stem cells from Cynomolgus monkey
title_short Establishment of a translational endothelial cell model using directed differentiation of induced pluripotent stem cells from Cynomolgus monkey
title_sort establishment of a translational endothelial cell model using directed differentiation of induced pluripotent stem cells from cynomolgus monkey
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5078800/
https://www.ncbi.nlm.nih.gov/pubmed/27779219
http://dx.doi.org/10.1038/srep35830
work_keys_str_mv AT thomaevac establishmentofatranslationalendothelialcellmodelusingdirecteddifferentiationofinducedpluripotentstemcellsfromcynomolgusmonkey
AT heckeltobias establishmentofatranslationalendothelialcellmodelusingdirecteddifferentiationofinducedpluripotentstemcellsfromcynomolgusmonkey
AT kellerdavid establishmentofatranslationalendothelialcellmodelusingdirecteddifferentiationofinducedpluripotentstemcellsfromcynomolgusmonkey
AT giroudnicolas establishmentofatranslationalendothelialcellmodelusingdirecteddifferentiationofinducedpluripotentstemcellsfromcynomolgusmonkey
AT leonardbrian establishmentofatranslationalendothelialcellmodelusingdirecteddifferentiationofinducedpluripotentstemcellsfromcynomolgusmonkey
AT christensenklaus establishmentofatranslationalendothelialcellmodelusingdirecteddifferentiationofinducedpluripotentstemcellsfromcynomolgusmonkey
AT rothadrian establishmentofatranslationalendothelialcellmodelusingdirecteddifferentiationofinducedpluripotentstemcellsfromcynomolgusmonkey
AT bertinettilapatkicristina establishmentofatranslationalendothelialcellmodelusingdirecteddifferentiationofinducedpluripotentstemcellsfromcynomolgusmonkey
AT grafmartin establishmentofatranslationalendothelialcellmodelusingdirecteddifferentiationofinducedpluripotentstemcellsfromcynomolgusmonkey
AT patschchristoph establishmentofatranslationalendothelialcellmodelusingdirecteddifferentiationofinducedpluripotentstemcellsfromcynomolgusmonkey