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Enhanced self-renewal of human pluripotent stem cells by simulated microgravity
A systematic study on the biological effects of simulated microgravity (sµg) on human pluripotent stem cells (hPSC) is still lacking. Here, we used a fast-rotating 2-D clinostat to investigate the sµg effect on proliferation, self-renewal, and cell cycle regulation of hPSCs. We observed significant...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9253108/ https://www.ncbi.nlm.nih.gov/pubmed/35787634 http://dx.doi.org/10.1038/s41526-022-00209-4 |
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author | Timilsina, S. Kirsch-Mangu, T. Werth, S. Shepard, B. Ma, T. Villa-Diaz, L. G. |
author_facet | Timilsina, S. Kirsch-Mangu, T. Werth, S. Shepard, B. Ma, T. Villa-Diaz, L. G. |
author_sort | Timilsina, S. |
collection | PubMed |
description | A systematic study on the biological effects of simulated microgravity (sµg) on human pluripotent stem cells (hPSC) is still lacking. Here, we used a fast-rotating 2-D clinostat to investigate the sµg effect on proliferation, self-renewal, and cell cycle regulation of hPSCs. We observed significant upregulation of protein translation of pluripotent transcription factors in hPSC cultured in sµg compared to cells cultured in 1g conditions. In addition to a significant increase in expression of telomere elongation genes. Differentiation experiments showed that hPSC cultured in sµg condition were less susceptible to differentiation compared to cells in 1g conditions. These results suggest that sµg enhances hPSC self-renewal. Our study revealed that sµg enhanced the cell proliferation of hPSCs by regulating the expression of cell cycle-associated kinases. RNA-seq analysis indicated that in sµg condition the expression of differentiation and development pathways are downregulated, while multiple components of the ubiquitin proteasome system are upregulated, contributing to an enhanced self-renewal of hPSCs. These effects of sµg were not replicated in human fibroblasts. Taken together, our results highlight pathways and mechanisms in hPSCs vulnerable to microgravity that imposes significant impacts on human health and performance, physiology, and cellular and molecular processes. |
format | Online Article Text |
id | pubmed-9253108 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-92531082022-07-06 Enhanced self-renewal of human pluripotent stem cells by simulated microgravity Timilsina, S. Kirsch-Mangu, T. Werth, S. Shepard, B. Ma, T. Villa-Diaz, L. G. NPJ Microgravity Article A systematic study on the biological effects of simulated microgravity (sµg) on human pluripotent stem cells (hPSC) is still lacking. Here, we used a fast-rotating 2-D clinostat to investigate the sµg effect on proliferation, self-renewal, and cell cycle regulation of hPSCs. We observed significant upregulation of protein translation of pluripotent transcription factors in hPSC cultured in sµg compared to cells cultured in 1g conditions. In addition to a significant increase in expression of telomere elongation genes. Differentiation experiments showed that hPSC cultured in sµg condition were less susceptible to differentiation compared to cells in 1g conditions. These results suggest that sµg enhances hPSC self-renewal. Our study revealed that sµg enhanced the cell proliferation of hPSCs by regulating the expression of cell cycle-associated kinases. RNA-seq analysis indicated that in sµg condition the expression of differentiation and development pathways are downregulated, while multiple components of the ubiquitin proteasome system are upregulated, contributing to an enhanced self-renewal of hPSCs. These effects of sµg were not replicated in human fibroblasts. Taken together, our results highlight pathways and mechanisms in hPSCs vulnerable to microgravity that imposes significant impacts on human health and performance, physiology, and cellular and molecular processes. Nature Publishing Group UK 2022-07-04 /pmc/articles/PMC9253108/ /pubmed/35787634 http://dx.doi.org/10.1038/s41526-022-00209-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Timilsina, S. Kirsch-Mangu, T. Werth, S. Shepard, B. Ma, T. Villa-Diaz, L. G. Enhanced self-renewal of human pluripotent stem cells by simulated microgravity |
title | Enhanced self-renewal of human pluripotent stem cells by simulated microgravity |
title_full | Enhanced self-renewal of human pluripotent stem cells by simulated microgravity |
title_fullStr | Enhanced self-renewal of human pluripotent stem cells by simulated microgravity |
title_full_unstemmed | Enhanced self-renewal of human pluripotent stem cells by simulated microgravity |
title_short | Enhanced self-renewal of human pluripotent stem cells by simulated microgravity |
title_sort | enhanced self-renewal of human pluripotent stem cells by simulated microgravity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9253108/ https://www.ncbi.nlm.nih.gov/pubmed/35787634 http://dx.doi.org/10.1038/s41526-022-00209-4 |
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