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The Low Toxicity of Graphene Quantum Dots is Reflected by Marginal Gene Expression Changes of Primary Human Hematopoietic Stem Cells

Graphene quantum dots (GQDs) are a promising next generation nanomaterial with manifold biomedical applications. For real world applications, comprehensive studies on their influence on the functionality of primary human cells are mandatory. Here, we report the effects of GQDs on the transcriptome o...

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Autores principales: Fasbender, Stefan, Zimmermann, Lisa, Cadeddu, Ron-Patrick, Luysberg, Martina, Moll, Bastian, Janiak, Christoph, Heinzel, Thomas, Haas, Rainer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6700176/
https://www.ncbi.nlm.nih.gov/pubmed/31427693
http://dx.doi.org/10.1038/s41598-019-48567-6
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author Fasbender, Stefan
Zimmermann, Lisa
Cadeddu, Ron-Patrick
Luysberg, Martina
Moll, Bastian
Janiak, Christoph
Heinzel, Thomas
Haas, Rainer
author_facet Fasbender, Stefan
Zimmermann, Lisa
Cadeddu, Ron-Patrick
Luysberg, Martina
Moll, Bastian
Janiak, Christoph
Heinzel, Thomas
Haas, Rainer
author_sort Fasbender, Stefan
collection PubMed
description Graphene quantum dots (GQDs) are a promising next generation nanomaterial with manifold biomedical applications. For real world applications, comprehensive studies on their influence on the functionality of primary human cells are mandatory. Here, we report the effects of GQDs on the transcriptome of CD34(+) hematopoietic stem cells after an incubation time of 36 hours. Of the 20 800 recorded gene expressions, only one, namely the selenoprotein W, 1, is changed by the GQDs in direct comparison to CD34(+) hematopoietic stem cells cultivated without GQDs. Only a meta analysis reveals that the expression of 1171 genes is weakly affected, taking into account the more prominent changes just by the cell culture. Eight corresponding, weakly affected signaling pathways are identified, which include, but are not limited to, the triggering of apoptosis. These results suggest that GQDs with sizes in the range of a few nanometers hardly influence the CD34(+) cells on the transcriptome level after 36 h of incubation, thereby demonstrating their high usability for in vivo studies, such as fluorescence labeling or delivery protocols, without strong effects on the functional status of the cells.
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spelling pubmed-67001762019-08-21 The Low Toxicity of Graphene Quantum Dots is Reflected by Marginal Gene Expression Changes of Primary Human Hematopoietic Stem Cells Fasbender, Stefan Zimmermann, Lisa Cadeddu, Ron-Patrick Luysberg, Martina Moll, Bastian Janiak, Christoph Heinzel, Thomas Haas, Rainer Sci Rep Article Graphene quantum dots (GQDs) are a promising next generation nanomaterial with manifold biomedical applications. For real world applications, comprehensive studies on their influence on the functionality of primary human cells are mandatory. Here, we report the effects of GQDs on the transcriptome of CD34(+) hematopoietic stem cells after an incubation time of 36 hours. Of the 20 800 recorded gene expressions, only one, namely the selenoprotein W, 1, is changed by the GQDs in direct comparison to CD34(+) hematopoietic stem cells cultivated without GQDs. Only a meta analysis reveals that the expression of 1171 genes is weakly affected, taking into account the more prominent changes just by the cell culture. Eight corresponding, weakly affected signaling pathways are identified, which include, but are not limited to, the triggering of apoptosis. These results suggest that GQDs with sizes in the range of a few nanometers hardly influence the CD34(+) cells on the transcriptome level after 36 h of incubation, thereby demonstrating their high usability for in vivo studies, such as fluorescence labeling or delivery protocols, without strong effects on the functional status of the cells. Nature Publishing Group UK 2019-08-19 /pmc/articles/PMC6700176/ /pubmed/31427693 http://dx.doi.org/10.1038/s41598-019-48567-6 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Fasbender, Stefan
Zimmermann, Lisa
Cadeddu, Ron-Patrick
Luysberg, Martina
Moll, Bastian
Janiak, Christoph
Heinzel, Thomas
Haas, Rainer
The Low Toxicity of Graphene Quantum Dots is Reflected by Marginal Gene Expression Changes of Primary Human Hematopoietic Stem Cells
title The Low Toxicity of Graphene Quantum Dots is Reflected by Marginal Gene Expression Changes of Primary Human Hematopoietic Stem Cells
title_full The Low Toxicity of Graphene Quantum Dots is Reflected by Marginal Gene Expression Changes of Primary Human Hematopoietic Stem Cells
title_fullStr The Low Toxicity of Graphene Quantum Dots is Reflected by Marginal Gene Expression Changes of Primary Human Hematopoietic Stem Cells
title_full_unstemmed The Low Toxicity of Graphene Quantum Dots is Reflected by Marginal Gene Expression Changes of Primary Human Hematopoietic Stem Cells
title_short The Low Toxicity of Graphene Quantum Dots is Reflected by Marginal Gene Expression Changes of Primary Human Hematopoietic Stem Cells
title_sort low toxicity of graphene quantum dots is reflected by marginal gene expression changes of primary human hematopoietic stem cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6700176/
https://www.ncbi.nlm.nih.gov/pubmed/31427693
http://dx.doi.org/10.1038/s41598-019-48567-6
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