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...
Autores principales: | , , , , , , , , , |
---|---|
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 |