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Nanog induced intermediate state in regulating stem cell differentiation and reprogramming
BACKGROUND: Heterogeneous gene expressions of cells are widely observed in self-renewing pluripotent stem cells, suggesting possible coexistence of multiple cellular states with distinct characteristics. Though the elements regulating cellular states have been identified, the underlying dynamic mech...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6389130/ https://www.ncbi.nlm.nih.gov/pubmed/29486740 http://dx.doi.org/10.1186/s12918-018-0552-3 |
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author | Yu, Peijia Nie, Qing Tang, Chao Zhang, Lei |
author_facet | Yu, Peijia Nie, Qing Tang, Chao Zhang, Lei |
author_sort | Yu, Peijia |
collection | PubMed |
description | BACKGROUND: Heterogeneous gene expressions of cells are widely observed in self-renewing pluripotent stem cells, suggesting possible coexistence of multiple cellular states with distinct characteristics. Though the elements regulating cellular states have been identified, the underlying dynamic mechanisms and the significance of such cellular heterogeneity remain elusive. RESULTS: We present a gene regulatory network model to investigate the bimodal Nanog distribution in stem cells. Our model reveals a novel role of dynamic conversion between the cellular states of high and low Nanog levels. Model simulations demonstrate that the low-Nanog state benefits cell differentiation through serving as an intermediate state to reduce the barrier of transition. Interestingly, the existence of low-Nanog state dynamically slows down the reprogramming process, and additional Nanog activation is found to be essential to quickly attaining the fully reprogrammed cell state. CONCLUSIONS: Nanog has been recognized as a critical pluripotency gene in stem cell regulation. Our modeling results quantitatively show a dual role of Nanog during stem cell differentiation and reprogramming, and the importance of the intermediate state during cell state transitions. Our approach offers a general method for analyzing key regulatory factors controlling cell differentiation and reprogramming. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12918-018-0552-3) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6389130 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-63891302019-03-19 Nanog induced intermediate state in regulating stem cell differentiation and reprogramming Yu, Peijia Nie, Qing Tang, Chao Zhang, Lei BMC Syst Biol Research Article BACKGROUND: Heterogeneous gene expressions of cells are widely observed in self-renewing pluripotent stem cells, suggesting possible coexistence of multiple cellular states with distinct characteristics. Though the elements regulating cellular states have been identified, the underlying dynamic mechanisms and the significance of such cellular heterogeneity remain elusive. RESULTS: We present a gene regulatory network model to investigate the bimodal Nanog distribution in stem cells. Our model reveals a novel role of dynamic conversion between the cellular states of high and low Nanog levels. Model simulations demonstrate that the low-Nanog state benefits cell differentiation through serving as an intermediate state to reduce the barrier of transition. Interestingly, the existence of low-Nanog state dynamically slows down the reprogramming process, and additional Nanog activation is found to be essential to quickly attaining the fully reprogrammed cell state. CONCLUSIONS: Nanog has been recognized as a critical pluripotency gene in stem cell regulation. Our modeling results quantitatively show a dual role of Nanog during stem cell differentiation and reprogramming, and the importance of the intermediate state during cell state transitions. Our approach offers a general method for analyzing key regulatory factors controlling cell differentiation and reprogramming. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12918-018-0552-3) contains supplementary material, which is available to authorized users. BioMed Central 2018-02-27 /pmc/articles/PMC6389130/ /pubmed/29486740 http://dx.doi.org/10.1186/s12918-018-0552-3 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Yu, Peijia Nie, Qing Tang, Chao Zhang, Lei Nanog induced intermediate state in regulating stem cell differentiation and reprogramming |
title | Nanog induced intermediate state in regulating stem cell differentiation and reprogramming |
title_full | Nanog induced intermediate state in regulating stem cell differentiation and reprogramming |
title_fullStr | Nanog induced intermediate state in regulating stem cell differentiation and reprogramming |
title_full_unstemmed | Nanog induced intermediate state in regulating stem cell differentiation and reprogramming |
title_short | Nanog induced intermediate state in regulating stem cell differentiation and reprogramming |
title_sort | nanog induced intermediate state in regulating stem cell differentiation and reprogramming |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6389130/ https://www.ncbi.nlm.nih.gov/pubmed/29486740 http://dx.doi.org/10.1186/s12918-018-0552-3 |
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