Periostin as a Biomarker of the Amniotic Membrane

Tracing the precise developmental origin of amnion and amnion-derived stem cells is still challenging and depends chiefly on analyzing powerful genetic model amniotes like mouse. Profound understanding of the fundamental differences in amnion development in both the disc-shaped primate and human emb...

Full description

Saved in:
Bibliographic Details
Main Authors: Mariya P. Dobreva, Larissa Lhoest, Paulo N. G. Pereira, Lieve Umans, Susana M. Chuva de Sousa Lopes, An Zwijsen
Format: Article
Language:English
Published: Wiley 2012-01-01
Series:Stem Cells International
Online Access:http://dx.doi.org/10.1155/2012/987185
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1832551453428809728
author Mariya P. Dobreva
Larissa Lhoest
Paulo N. G. Pereira
Lieve Umans
Susana M. Chuva de Sousa Lopes
An Zwijsen
author_facet Mariya P. Dobreva
Larissa Lhoest
Paulo N. G. Pereira
Lieve Umans
Susana M. Chuva de Sousa Lopes
An Zwijsen
author_sort Mariya P. Dobreva
collection DOAJ
description Tracing the precise developmental origin of amnion and amnion-derived stem cells is still challenging and depends chiefly on analyzing powerful genetic model amniotes like mouse. Profound understanding of the fundamental differences in amnion development in both the disc-shaped primate and human embryo and the cup-shaped mouse embryo is pivotal in particular when sampling amniotic membrane from nonprimate species for isolating candidate amniotic stem cells. The availability of molecular marker genes that are specifically expressed in the amniotic membrane and not in other extraembryonic membranes would be instrumental to validate unequivocally the starting material under investigation. So far such amniotic markers have not been reported. We postulated that bone morphogenetic protein (BMP) target genes are putative amniotic membrane markers mainly because deficiency in one of several components of the BMP signaling cascade in mice has been documented to result in defective development of the early amnion. Comparative gene expression analysis of acknowledged target genes for BMP in different extraembryonic tissues, combined with in situ hybridization, identified Periostin (Postn) mRNA enrichment in amnion throughout gestation. In addition, we identify and propose a combination of markers as transcriptional signature for the different extraembryonic tissues in mouse.
format Article
id doaj-art-393dc05b5746448ab18524c1cc59c9dd
institution Kabale University
issn 1687-966X
1687-9678
language English
publishDate 2012-01-01
publisher Wiley
record_format Article
series Stem Cells International
spelling doaj-art-393dc05b5746448ab18524c1cc59c9dd2025-02-03T06:01:19ZengWileyStem Cells International1687-966X1687-96782012-01-01201210.1155/2012/987185987185Periostin as a Biomarker of the Amniotic MembraneMariya P. Dobreva0Larissa Lhoest1Paulo N. G. Pereira2Lieve Umans3Susana M. Chuva de Sousa Lopes4An Zwijsen5Laboratory of Developmental Signaling, VIB11 Center for the Biology of Disease, VIB, 3000 Leuven, BelgiumLaboratory of Developmental Signaling, VIB11 Center for the Biology of Disease, VIB, 3000 Leuven, BelgiumLaboratory of Developmental Signaling, VIB11 Center for the Biology of Disease, VIB, 3000 Leuven, BelgiumLaboratory of Molecular Biology (Celgen), Department of Development and Regeneration, KU Leuven, 3000 Leuven, BelgiumDepartment of Anatomy and Embryology, Leiden University Medical Centre, 2333 ZC Leiden, The NetherlandsLaboratory of Developmental Signaling, VIB11 Center for the Biology of Disease, VIB, 3000 Leuven, BelgiumTracing the precise developmental origin of amnion and amnion-derived stem cells is still challenging and depends chiefly on analyzing powerful genetic model amniotes like mouse. Profound understanding of the fundamental differences in amnion development in both the disc-shaped primate and human embryo and the cup-shaped mouse embryo is pivotal in particular when sampling amniotic membrane from nonprimate species for isolating candidate amniotic stem cells. The availability of molecular marker genes that are specifically expressed in the amniotic membrane and not in other extraembryonic membranes would be instrumental to validate unequivocally the starting material under investigation. So far such amniotic markers have not been reported. We postulated that bone morphogenetic protein (BMP) target genes are putative amniotic membrane markers mainly because deficiency in one of several components of the BMP signaling cascade in mice has been documented to result in defective development of the early amnion. Comparative gene expression analysis of acknowledged target genes for BMP in different extraembryonic tissues, combined with in situ hybridization, identified Periostin (Postn) mRNA enrichment in amnion throughout gestation. In addition, we identify and propose a combination of markers as transcriptional signature for the different extraembryonic tissues in mouse.http://dx.doi.org/10.1155/2012/987185
spellingShingle Mariya P. Dobreva
Larissa Lhoest
Paulo N. G. Pereira
Lieve Umans
Susana M. Chuva de Sousa Lopes
An Zwijsen
Periostin as a Biomarker of the Amniotic Membrane
Stem Cells International
title Periostin as a Biomarker of the Amniotic Membrane
title_full Periostin as a Biomarker of the Amniotic Membrane
title_fullStr Periostin as a Biomarker of the Amniotic Membrane
title_full_unstemmed Periostin as a Biomarker of the Amniotic Membrane
title_short Periostin as a Biomarker of the Amniotic Membrane
title_sort periostin as a biomarker of the amniotic membrane
url http://dx.doi.org/10.1155/2012/987185
work_keys_str_mv AT mariyapdobreva periostinasabiomarkeroftheamnioticmembrane
AT larissalhoest periostinasabiomarkeroftheamnioticmembrane
AT paulongpereira periostinasabiomarkeroftheamnioticmembrane
AT lieveumans periostinasabiomarkeroftheamnioticmembrane
AT susanamchuvadesousalopes periostinasabiomarkeroftheamnioticmembrane
AT anzwijsen periostinasabiomarkeroftheamnioticmembrane