Direct comparison of distinct naive pluripotent states in human embryonic stem cells

Human embryonic stem cells (hESCs) in culture display a state of primed pluripotency, but recent protocols have been developed that enable hESCs to adopt a naive-like pluripotent state. Here the authors perform a side-by-side comparison of methods used to culture naive hESCs and confirm the role of...

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Main Authors: S. Warrier, M. Van der Jeught, G. Duggal, L. Tilleman, E. Sutherland, J. Taelman, M. Popovic, S. Lierman, S. Chuva De Sousa Lopes, A. Van Soom, L. Peelman, F. Van Nieuwerburgh, D. I. M. De Coninck, B. Menten, P. Mestdagh, J. Van de Sompele, D. Deforce, P. De Sutter, B. Heindryckx
Format: Article
Language:English
Published: Nature Portfolio 2017-04-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/ncomms15055
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author S. Warrier
M. Van der Jeught
G. Duggal
L. Tilleman
E. Sutherland
J. Taelman
M. Popovic
S. Lierman
S. Chuva De Sousa Lopes
A. Van Soom
L. Peelman
F. Van Nieuwerburgh
D. I. M. De Coninck
B. Menten
P. Mestdagh
J. Van de Sompele
D. Deforce
P. De Sutter
B. Heindryckx
author_facet S. Warrier
M. Van der Jeught
G. Duggal
L. Tilleman
E. Sutherland
J. Taelman
M. Popovic
S. Lierman
S. Chuva De Sousa Lopes
A. Van Soom
L. Peelman
F. Van Nieuwerburgh
D. I. M. De Coninck
B. Menten
P. Mestdagh
J. Van de Sompele
D. Deforce
P. De Sutter
B. Heindryckx
author_sort S. Warrier
collection DOAJ
description Human embryonic stem cells (hESCs) in culture display a state of primed pluripotency, but recent protocols have been developed that enable hESCs to adopt a naive-like pluripotent state. Here the authors perform a side-by-side comparison of methods used to culture naive hESCs and confirm the role of PI3K/AKT/mTORC signalling in facilitating the induction of naive pluripotency.
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spelling doaj.art-244cbf649add464c82660353beddd9822022-12-21T20:28:48ZengNature PortfolioNature Communications2041-17232017-04-018111010.1038/ncomms15055Direct comparison of distinct naive pluripotent states in human embryonic stem cellsS. Warrier0M. Van der Jeught1G. Duggal2L. Tilleman3E. Sutherland4J. Taelman5M. Popovic6S. Lierman7S. Chuva De Sousa Lopes8A. Van Soom9L. Peelman10F. Van Nieuwerburgh11D. I. M. De Coninck12B. Menten13P. Mestdagh14J. Van de Sompele15D. Deforce16P. De Sutter17B. Heindryckx18Department for Reproductive Medicine, Ghent-Fertility and Stem cell Team (G-FaST), Ghent University HospitalDepartment for Reproductive Medicine, Ghent-Fertility and Stem cell Team (G-FaST), Ghent University HospitalDepartment for Reproductive Medicine, Ghent-Fertility and Stem cell Team (G-FaST), Ghent University HospitalDepartment of Pharmaceutics, Laboratory for Pharmaceutical Biotechnology, Faculty of Pharmaceutical Sciences, Ghent UniversityDepartment for Reproductive Medicine, Ghent-Fertility and Stem cell Team (G-FaST), Ghent University HospitalDepartment for Reproductive Medicine, Ghent-Fertility and Stem cell Team (G-FaST), Ghent University HospitalDepartment for Reproductive Medicine, Ghent-Fertility and Stem cell Team (G-FaST), Ghent University HospitalDepartment for Reproductive Medicine, Ghent-Fertility and Stem cell Team (G-FaST), Ghent University HospitalDepartment for Reproductive Medicine, Ghent-Fertility and Stem cell Team (G-FaST), Ghent University HospitalDepartment of Reproduction, Obstetrics and Herd Health, Faculty of Veterinary Medicine, Ghent UniversityDepartment of Nutrition, Genetics and Ethology, Faculty of Veterinary Medicine, Ghent UniversityDepartment of Pharmaceutics, Laboratory for Pharmaceutical Biotechnology, Faculty of Pharmaceutical Sciences, Ghent UniversityDepartment of Pharmaceutics, Laboratory for Pharmaceutical Biotechnology, Faculty of Pharmaceutical Sciences, Ghent UniversityDepartment of Pediatrics and Medical Genetics, Center for Medical Genetics, Ghent University HospitalDepartment of Pediatrics and Medical Genetics, Center for Medical Genetics, Ghent University HospitalDepartment of Pediatrics and Medical Genetics, Center for Medical Genetics, Ghent University HospitalDepartment of Pharmaceutics, Laboratory for Pharmaceutical Biotechnology, Faculty of Pharmaceutical Sciences, Ghent UniversityDepartment for Reproductive Medicine, Ghent-Fertility and Stem cell Team (G-FaST), Ghent University HospitalDepartment for Reproductive Medicine, Ghent-Fertility and Stem cell Team (G-FaST), Ghent University HospitalHuman embryonic stem cells (hESCs) in culture display a state of primed pluripotency, but recent protocols have been developed that enable hESCs to adopt a naive-like pluripotent state. Here the authors perform a side-by-side comparison of methods used to culture naive hESCs and confirm the role of PI3K/AKT/mTORC signalling in facilitating the induction of naive pluripotency.https://doi.org/10.1038/ncomms15055
spellingShingle S. Warrier
M. Van der Jeught
G. Duggal
L. Tilleman
E. Sutherland
J. Taelman
M. Popovic
S. Lierman
S. Chuva De Sousa Lopes
A. Van Soom
L. Peelman
F. Van Nieuwerburgh
D. I. M. De Coninck
B. Menten
P. Mestdagh
J. Van de Sompele
D. Deforce
P. De Sutter
B. Heindryckx
Direct comparison of distinct naive pluripotent states in human embryonic stem cells
Nature Communications
title Direct comparison of distinct naive pluripotent states in human embryonic stem cells
title_full Direct comparison of distinct naive pluripotent states in human embryonic stem cells
title_fullStr Direct comparison of distinct naive pluripotent states in human embryonic stem cells
title_full_unstemmed Direct comparison of distinct naive pluripotent states in human embryonic stem cells
title_short Direct comparison of distinct naive pluripotent states in human embryonic stem cells
title_sort direct comparison of distinct naive pluripotent states in human embryonic stem cells
url https://doi.org/10.1038/ncomms15055
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