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Trib2 regulates the pluripotency of embryonic stem cells and enhances reprogramming efficiency

Embryonic stem (ES) cells are pluripotent cells characterized by self-renewability and differentiation potential. Induced pluripotent stem (iPS) cells are ES cell-equivalent cells derived from somatic cells by the introduction of core reprogramming factors. ES and iPS cells are important sources for...

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Autores principales: Do, Eun Kyoung, Park, Jae Kyung, Cheon, Hyo Cheon, Kwon, Yang Woo, Heo, Soon Chul, Choi, Eun Jung, Seo, Jeong Kon, Jang, Il Ho, Lee, Sang Chul, Kim, Jae Ho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5704193/
https://www.ncbi.nlm.nih.gov/pubmed/29170476
http://dx.doi.org/10.1038/emm.2017.191
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author Do, Eun Kyoung
Park, Jae Kyung
Cheon, Hyo Cheon
Kwon, Yang Woo
Heo, Soon Chul
Choi, Eun Jung
Seo, Jeong Kon
Jang, Il Ho
Lee, Sang Chul
Kim, Jae Ho
author_facet Do, Eun Kyoung
Park, Jae Kyung
Cheon, Hyo Cheon
Kwon, Yang Woo
Heo, Soon Chul
Choi, Eun Jung
Seo, Jeong Kon
Jang, Il Ho
Lee, Sang Chul
Kim, Jae Ho
author_sort Do, Eun Kyoung
collection PubMed
description Embryonic stem (ES) cells are pluripotent cells characterized by self-renewability and differentiation potential. Induced pluripotent stem (iPS) cells are ES cell-equivalent cells derived from somatic cells by the introduction of core reprogramming factors. ES and iPS cells are important sources for understanding basic biology and for generating therapeutic cells for clinical applications. Tribbles homolog 2 (Trib2) functions as a scaffold in signaling pathways. However, the relevance of Trib2 to the pluripotency of ES and iPS cells is unknown. In the present study, we elucidated the importance of Trib2 in maintaining pluripotency in mouse ES cells and in generating iPS cells from somatic cells through the reprogramming process. Trib2 expression decreased as ES cells differentiated, and Trib2 knockdown in ES cells changed their colony morphology while reducing the activity of alkaline phosphatase and the expression of the pluripotency marker genes Oct4, Sox2, Nanog and Klf4. Trib2 directly interacted with Oct4 and elevated Oct4 promoter activity. During the generation of iPS cells, Trib2 knockdown decreased the reprogramming efficiency of mouse embryonic fibroblasts, whereas Trib2 overexpression significantly increased their reprogramming efficiency. In summary, our results suggest that Trib2 is important for maintaining self-renewal in ES cells and for pluripotency induction during the reprogramming process.
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spelling pubmed-57041932017-12-07 Trib2 regulates the pluripotency of embryonic stem cells and enhances reprogramming efficiency Do, Eun Kyoung Park, Jae Kyung Cheon, Hyo Cheon Kwon, Yang Woo Heo, Soon Chul Choi, Eun Jung Seo, Jeong Kon Jang, Il Ho Lee, Sang Chul Kim, Jae Ho Exp Mol Med Original Article Embryonic stem (ES) cells are pluripotent cells characterized by self-renewability and differentiation potential. Induced pluripotent stem (iPS) cells are ES cell-equivalent cells derived from somatic cells by the introduction of core reprogramming factors. ES and iPS cells are important sources for understanding basic biology and for generating therapeutic cells for clinical applications. Tribbles homolog 2 (Trib2) functions as a scaffold in signaling pathways. However, the relevance of Trib2 to the pluripotency of ES and iPS cells is unknown. In the present study, we elucidated the importance of Trib2 in maintaining pluripotency in mouse ES cells and in generating iPS cells from somatic cells through the reprogramming process. Trib2 expression decreased as ES cells differentiated, and Trib2 knockdown in ES cells changed their colony morphology while reducing the activity of alkaline phosphatase and the expression of the pluripotency marker genes Oct4, Sox2, Nanog and Klf4. Trib2 directly interacted with Oct4 and elevated Oct4 promoter activity. During the generation of iPS cells, Trib2 knockdown decreased the reprogramming efficiency of mouse embryonic fibroblasts, whereas Trib2 overexpression significantly increased their reprogramming efficiency. In summary, our results suggest that Trib2 is important for maintaining self-renewal in ES cells and for pluripotency induction during the reprogramming process. Nature Publishing Group 2017-11 2017-11-24 /pmc/articles/PMC5704193/ /pubmed/29170476 http://dx.doi.org/10.1038/emm.2017.191 Text en Copyright © 2017 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 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-nc-nd/4.0/
spellingShingle Original Article
Do, Eun Kyoung
Park, Jae Kyung
Cheon, Hyo Cheon
Kwon, Yang Woo
Heo, Soon Chul
Choi, Eun Jung
Seo, Jeong Kon
Jang, Il Ho
Lee, Sang Chul
Kim, Jae Ho
Trib2 regulates the pluripotency of embryonic stem cells and enhances reprogramming efficiency
title Trib2 regulates the pluripotency of embryonic stem cells and enhances reprogramming efficiency
title_full Trib2 regulates the pluripotency of embryonic stem cells and enhances reprogramming efficiency
title_fullStr Trib2 regulates the pluripotency of embryonic stem cells and enhances reprogramming efficiency
title_full_unstemmed Trib2 regulates the pluripotency of embryonic stem cells and enhances reprogramming efficiency
title_short Trib2 regulates the pluripotency of embryonic stem cells and enhances reprogramming efficiency
title_sort trib2 regulates the pluripotency of embryonic stem cells and enhances reprogramming efficiency
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5704193/
https://www.ncbi.nlm.nih.gov/pubmed/29170476
http://dx.doi.org/10.1038/emm.2017.191
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