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Graphene Oxide promotes embryonic stem cell differentiation to haematopoietic lineage
Pluripotent stem cells represent a promising source of differentiated tissue-specific stem and multipotent progenitor cells for regenerative medicine and drug testing. The realisation of this potential relies on the establishment of robust and reproducible protocols of differentiation. Several repor...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4873758/ https://www.ncbi.nlm.nih.gov/pubmed/27197878 http://dx.doi.org/10.1038/srep25917 |
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author | Garcia-Alegria, Eva Iluit, Maria Stefanska, Monika Silva, Claudio Heeg, Sebastian Kimber, Susan J. Kouskoff, Valerie Lacaud, Georges Vijayaraghavan, Aravind Batta, Kiran |
author_facet | Garcia-Alegria, Eva Iluit, Maria Stefanska, Monika Silva, Claudio Heeg, Sebastian Kimber, Susan J. Kouskoff, Valerie Lacaud, Georges Vijayaraghavan, Aravind Batta, Kiran |
author_sort | Garcia-Alegria, Eva |
collection | PubMed |
description | Pluripotent stem cells represent a promising source of differentiated tissue-specific stem and multipotent progenitor cells for regenerative medicine and drug testing. The realisation of this potential relies on the establishment of robust and reproducible protocols of differentiation. Several reports have highlighted the importance of biomaterials in assisting directed differentiation. Graphene oxide (GO) is a novel material that has attracted increasing interest in the field of biomedicine. In this study, we demonstrate that GO coated substrates significantly enhance the differentiation of mouse embryonic stem (ES) cells to both primitive and definitive haematopoietic cells. GO does not affect cell proliferation or survival of differentiated cells but rather enhances the transition of haemangioblasts to haemogenic endothelial cells, a key step during haematopoietic specification. Importantly, GO also improves, in addition to murine, human ES cell differentiation to blood cells. Taken together, our study reveals a positive role for GO in haematopoietic differentiation and suggests that further functionalization of GO could represent a valid strategy for the generation of large numbers of functional blood cells. Producing these cells would accelerate haematopoietic drug toxicity testing and treatment of patients with blood disorders or malignancies. |
format | Online Article Text |
id | pubmed-4873758 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48737582016-06-02 Graphene Oxide promotes embryonic stem cell differentiation to haematopoietic lineage Garcia-Alegria, Eva Iluit, Maria Stefanska, Monika Silva, Claudio Heeg, Sebastian Kimber, Susan J. Kouskoff, Valerie Lacaud, Georges Vijayaraghavan, Aravind Batta, Kiran Sci Rep Article Pluripotent stem cells represent a promising source of differentiated tissue-specific stem and multipotent progenitor cells for regenerative medicine and drug testing. The realisation of this potential relies on the establishment of robust and reproducible protocols of differentiation. Several reports have highlighted the importance of biomaterials in assisting directed differentiation. Graphene oxide (GO) is a novel material that has attracted increasing interest in the field of biomedicine. In this study, we demonstrate that GO coated substrates significantly enhance the differentiation of mouse embryonic stem (ES) cells to both primitive and definitive haematopoietic cells. GO does not affect cell proliferation or survival of differentiated cells but rather enhances the transition of haemangioblasts to haemogenic endothelial cells, a key step during haematopoietic specification. Importantly, GO also improves, in addition to murine, human ES cell differentiation to blood cells. Taken together, our study reveals a positive role for GO in haematopoietic differentiation and suggests that further functionalization of GO could represent a valid strategy for the generation of large numbers of functional blood cells. Producing these cells would accelerate haematopoietic drug toxicity testing and treatment of patients with blood disorders or malignancies. Nature Publishing Group 2016-05-20 /pmc/articles/PMC4873758/ /pubmed/27197878 http://dx.doi.org/10.1038/srep25917 Text en Copyright © 2016, Macmillan Publishers Limited 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 Garcia-Alegria, Eva Iluit, Maria Stefanska, Monika Silva, Claudio Heeg, Sebastian Kimber, Susan J. Kouskoff, Valerie Lacaud, Georges Vijayaraghavan, Aravind Batta, Kiran Graphene Oxide promotes embryonic stem cell differentiation to haematopoietic lineage |
title | Graphene Oxide promotes embryonic stem cell differentiation to haematopoietic lineage |
title_full | Graphene Oxide promotes embryonic stem cell differentiation to haematopoietic lineage |
title_fullStr | Graphene Oxide promotes embryonic stem cell differentiation to haematopoietic lineage |
title_full_unstemmed | Graphene Oxide promotes embryonic stem cell differentiation to haematopoietic lineage |
title_short | Graphene Oxide promotes embryonic stem cell differentiation to haematopoietic lineage |
title_sort | graphene oxide promotes embryonic stem cell differentiation to haematopoietic lineage |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4873758/ https://www.ncbi.nlm.nih.gov/pubmed/27197878 http://dx.doi.org/10.1038/srep25917 |
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