Pluripotency Factors on Their Lineage Move

Pluripotent stem cells are characterised by continuous self-renewal while maintaining the potential to differentiate into cells of all three germ layers. Regulatory networks of maintaining pluripotency have been described in great detail and, similarly, there is great knowledge on key players that r...

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Main Authors: Clair E. Weidgang, Thomas Seufferlein, Alexander Kleger, Martin Mueller
Format: Article
Language:English
Published: Hindawi Limited 2016-01-01
Series:Stem Cells International
Online Access:http://dx.doi.org/10.1155/2016/6838253
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spelling doaj-b520583959e04c8abb617ec9f50bed2c2020-11-24T23:08:02ZengHindawi LimitedStem Cells International1687-966X1687-96782016-01-01201610.1155/2016/68382536838253Pluripotency Factors on Their Lineage MoveClair E. Weidgang0Thomas Seufferlein1Alexander Kleger2Martin Mueller3Department of Internal Medicine I, Ulm University Hospital, 89069 Ulm, GermanyDepartment of Internal Medicine I, Ulm University Hospital, 89069 Ulm, GermanyDepartment of Internal Medicine I, Ulm University Hospital, 89069 Ulm, GermanyDepartment of Internal Medicine I, Ulm University Hospital, 89069 Ulm, GermanyPluripotent stem cells are characterised by continuous self-renewal while maintaining the potential to differentiate into cells of all three germ layers. Regulatory networks of maintaining pluripotency have been described in great detail and, similarly, there is great knowledge on key players that regulate their differentiation. Interestingly, pluripotency has various shades with distinct developmental potential, an observation that coined the term of a ground state of pluripotency. A precise interplay of signalling axes regulates ground state conditions and acts in concert with a combination of key transcription factors. The balance between these transcription factors greatly influences the integrity of the pluripotency network and latest research suggests that minute changes in their expression can strengthen but also collapse the network. Moreover, recent studies reveal different facets of these core factors in balancing a controlled and directed exit from pluripotency. Thereby, subsets of pluripotency-maintaining factors have been shown to adopt new roles during lineage specification and have been globally defined towards neuroectodermal and mesendodermal sets of embryonic stem cell genes. However, detailed underlying insights into how these transcription factors orchestrate cell fate decisions remain largely elusive. Our group and others unravelled complex interactions in the regulation of this controlled exit. Herein, we summarise recent findings and discuss the potential mechanisms involved.http://dx.doi.org/10.1155/2016/6838253
collection DOAJ
language English
format Article
sources DOAJ
author Clair E. Weidgang
Thomas Seufferlein
Alexander Kleger
Martin Mueller
spellingShingle Clair E. Weidgang
Thomas Seufferlein
Alexander Kleger
Martin Mueller
Pluripotency Factors on Their Lineage Move
Stem Cells International
author_facet Clair E. Weidgang
Thomas Seufferlein
Alexander Kleger
Martin Mueller
author_sort Clair E. Weidgang
title Pluripotency Factors on Their Lineage Move
title_short Pluripotency Factors on Their Lineage Move
title_full Pluripotency Factors on Their Lineage Move
title_fullStr Pluripotency Factors on Their Lineage Move
title_full_unstemmed Pluripotency Factors on Their Lineage Move
title_sort pluripotency factors on their lineage move
publisher Hindawi Limited
series Stem Cells International
issn 1687-966X
1687-9678
publishDate 2016-01-01
description Pluripotent stem cells are characterised by continuous self-renewal while maintaining the potential to differentiate into cells of all three germ layers. Regulatory networks of maintaining pluripotency have been described in great detail and, similarly, there is great knowledge on key players that regulate their differentiation. Interestingly, pluripotency has various shades with distinct developmental potential, an observation that coined the term of a ground state of pluripotency. A precise interplay of signalling axes regulates ground state conditions and acts in concert with a combination of key transcription factors. The balance between these transcription factors greatly influences the integrity of the pluripotency network and latest research suggests that minute changes in their expression can strengthen but also collapse the network. Moreover, recent studies reveal different facets of these core factors in balancing a controlled and directed exit from pluripotency. Thereby, subsets of pluripotency-maintaining factors have been shown to adopt new roles during lineage specification and have been globally defined towards neuroectodermal and mesendodermal sets of embryonic stem cell genes. However, detailed underlying insights into how these transcription factors orchestrate cell fate decisions remain largely elusive. Our group and others unravelled complex interactions in the regulation of this controlled exit. Herein, we summarise recent findings and discuss the potential mechanisms involved.
url http://dx.doi.org/10.1155/2016/6838253
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