A Resource for the Transcriptional Signature of Bona Fide Trophoblast Stem Cells and Analysis of Their Embryonic Persistence

Trophoblast stem cells (TSCs) represent the multipotent progenitors that give rise to the different cells of the embryonic portion of the placenta. Here, we analysed the expression of key TSC transcription factors Cdx2, Eomes, and Elf5 in the early developing placenta of mouse embryos and in culture...

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Main Authors: Georg Kuales, Matthias Weiss, Oliver Sedelmeier, Dietmar Pfeifer, Sebastian J. Arnold
Format: Article
Language:English
Published: Wiley 2015-01-01
Series:Stem Cells International
Online Access:http://dx.doi.org/10.1155/2015/218518
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author Georg Kuales
Matthias Weiss
Oliver Sedelmeier
Dietmar Pfeifer
Sebastian J. Arnold
author_facet Georg Kuales
Matthias Weiss
Oliver Sedelmeier
Dietmar Pfeifer
Sebastian J. Arnold
author_sort Georg Kuales
collection DOAJ
description Trophoblast stem cells (TSCs) represent the multipotent progenitors that give rise to the different cells of the embryonic portion of the placenta. Here, we analysed the expression of key TSC transcription factors Cdx2, Eomes, and Elf5 in the early developing placenta of mouse embryos and in cultured TSCs and reveal surprising heterogeneity in protein levels. We analysed persistence of TSCs in the early placenta and find that TSCs remain in the chorionic hinge until E9.5 and are lost shortly afterwards. To define the transcriptional signature of bona fide TSCs, we used inducible gain- and loss-of-function alleles of Eomes or Cdx2, and EomesGFP, to manipulate and monitor the core maintenance factors of TSCs, followed by genome-wide expression profiling. Combinatorial analysis of resulting expression profiles allowed for defining novel TSC marker genes that might functionally contribute to the maintenance of the TSC state. Analyses by qRT-PCR and in situ hybridisation validated novel TSC- and chorion-specific marker genes, such as Bok/Mtd, Cldn26, Duox2, Duoxa2, Nr0b1, and Sox21. Thus, these expression data provide a valuable resource for the transcriptional signature of bona fide and early differentiating TSCs and may contribute to an increased understanding of the transcriptional circuitries that maintain and/or establish stemness of TSCs.
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spelling doaj-art-0274a7673690412ea000793d938470d72025-02-03T01:00:54ZengWileyStem Cells International1687-966X1687-96782015-01-01201510.1155/2015/218518218518A Resource for the Transcriptional Signature of Bona Fide Trophoblast Stem Cells and Analysis of Their Embryonic PersistenceGeorg Kuales0Matthias Weiss1Oliver Sedelmeier2Dietmar Pfeifer3Sebastian J. Arnold4Renal Department, Centre for Clinical Research, University Medical Centre, Breisacher Strasse 66, 79106 Freiburg, GermanyRenal Department, Centre for Clinical Research, University Medical Centre, Breisacher Strasse 66, 79106 Freiburg, GermanyRenal Department, Centre for Clinical Research, University Medical Centre, Breisacher Strasse 66, 79106 Freiburg, GermanyDepartment of Hematology, Oncology and Stem Cell Transplantation, University Medical Centre, Freiburg, GermanyRenal Department, Centre for Clinical Research, University Medical Centre, Breisacher Strasse 66, 79106 Freiburg, GermanyTrophoblast stem cells (TSCs) represent the multipotent progenitors that give rise to the different cells of the embryonic portion of the placenta. Here, we analysed the expression of key TSC transcription factors Cdx2, Eomes, and Elf5 in the early developing placenta of mouse embryos and in cultured TSCs and reveal surprising heterogeneity in protein levels. We analysed persistence of TSCs in the early placenta and find that TSCs remain in the chorionic hinge until E9.5 and are lost shortly afterwards. To define the transcriptional signature of bona fide TSCs, we used inducible gain- and loss-of-function alleles of Eomes or Cdx2, and EomesGFP, to manipulate and monitor the core maintenance factors of TSCs, followed by genome-wide expression profiling. Combinatorial analysis of resulting expression profiles allowed for defining novel TSC marker genes that might functionally contribute to the maintenance of the TSC state. Analyses by qRT-PCR and in situ hybridisation validated novel TSC- and chorion-specific marker genes, such as Bok/Mtd, Cldn26, Duox2, Duoxa2, Nr0b1, and Sox21. Thus, these expression data provide a valuable resource for the transcriptional signature of bona fide and early differentiating TSCs and may contribute to an increased understanding of the transcriptional circuitries that maintain and/or establish stemness of TSCs.http://dx.doi.org/10.1155/2015/218518
spellingShingle Georg Kuales
Matthias Weiss
Oliver Sedelmeier
Dietmar Pfeifer
Sebastian J. Arnold
A Resource for the Transcriptional Signature of Bona Fide Trophoblast Stem Cells and Analysis of Their Embryonic Persistence
Stem Cells International
title A Resource for the Transcriptional Signature of Bona Fide Trophoblast Stem Cells and Analysis of Their Embryonic Persistence
title_full A Resource for the Transcriptional Signature of Bona Fide Trophoblast Stem Cells and Analysis of Their Embryonic Persistence
title_fullStr A Resource for the Transcriptional Signature of Bona Fide Trophoblast Stem Cells and Analysis of Their Embryonic Persistence
title_full_unstemmed A Resource for the Transcriptional Signature of Bona Fide Trophoblast Stem Cells and Analysis of Their Embryonic Persistence
title_short A Resource for the Transcriptional Signature of Bona Fide Trophoblast Stem Cells and Analysis of Their Embryonic Persistence
title_sort resource for the transcriptional signature of bona fide trophoblast stem cells and analysis of their embryonic persistence
url http://dx.doi.org/10.1155/2015/218518
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