Syncytiotrophoblast Markers Are Downregulated in Placentas from Idiopathic Stillbirths.


Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
09 May 2024
Historique:
received: 01 04 2024
revised: 03 05 2024
accepted: 07 05 2024
medline: 25 5 2024
pubmed: 25 5 2024
entrez: 25 5 2024
Statut: epublish

Résumé

The trophoblast cells are responsible for the transfer of nutrients between the mother and the foetus and play a major role in placental endocrine function by producing and releasing large amounts of hormones and growth factors. Syncytiotrophoblast cells (STB), formed by the fusion of mononuclear cytotrophoblasts (CTB), constitute the interface between the foetus and the mother and are essential for all of these functions. We performed transcriptome analysis of human placental samples from two control groups-live births (LB), and stillbirths (SB) with a clinically recognised cause-and from our study group, idiopathic stillbirths (iSB). We identified 1172 DEGs in iSB, when comparing with the LB group; however, when we compared iSB with the SB group, only 15 and 12 genes were down- and upregulated in iSB, respectively. An assessment of these DEGs identified 15 commonly downregulated genes in iSB. Among these, several syncytiotrophoblast markers, like genes from the

Identifiants

pubmed: 38791219
pii: ijms25105180
doi: 10.3390/ijms25105180
pii:
doi:

Substances chimiques

Biomarkers 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Fundação para a Ciência e Tecnologia
ID : EXPL/MED-GEN/1261/2021
Organisme : Fundação para a Ciência e Tecnologia
ID : SFRH/BD/147440/2019
Organisme : Fundação para a Ciência e Tecnologia
ID : CEECIND/00371/2017
Organisme : Dutch Organization for Health Research and Development
ID : ZonMW PSIDER-2021-10250022120001
Organisme : Novo Nordisk Foundation
ID : reNEW NNF21CC0073729

Auteurs

Sara Vasconcelos (S)

Genetics Service, Department of Pathology, Faculty of Medicine, University of Porto, 4200-319 Porto, Portugal.
i3S-Instituto de Investigação e Inovação em Saúde, University of Porto, 4200-135 Porto, Portugal.

Ioannis Moustakas (I)

Department of Anatomy and Embryology, Leiden University Medical Center, 2333 ZC Leiden, The Netherlands.
Sequencing Analysis Support Core, Leiden University Medical Center, 2333 ZC Leiden, The Netherlands.

Miguel R Branco (MR)

Blizard Institute, Faculty of Medicine and Dentistry, Queen Mary University of London, London E1 2AT, UK.

Susana Guimarães (S)

Department of Pathology, Faculty of Medicine and Centro Hospitalar Universitário São João, 4200-319 Porto, Portugal.

Carla Caniçais (C)

Genetics Service, Department of Pathology, Faculty of Medicine, University of Porto, 4200-319 Porto, Portugal.
i3S-Instituto de Investigação e Inovação em Saúde, University of Porto, 4200-135 Porto, Portugal.

Talia van der Helm (TV)

Department of Anatomy and Embryology, Leiden University Medical Center, 2333 ZC Leiden, The Netherlands.

Carla Ramalho (C)

i3S-Instituto de Investigação e Inovação em Saúde, University of Porto, 4200-135 Porto, Portugal.
Department of Obstetrics and Gynaecology, Faculty of Medicine and Centro Hospitalar Universitário São João, 4200-319 Porto, Portugal.

Cristina Joana Marques (CJ)

Genetics Service, Department of Pathology, Faculty of Medicine, University of Porto, 4200-319 Porto, Portugal.
i3S-Instituto de Investigação e Inovação em Saúde, University of Porto, 4200-135 Porto, Portugal.

Susana M Chuva de Sousa Lopes (SMC)

Department of Anatomy and Embryology, Leiden University Medical Center, 2333 ZC Leiden, The Netherlands.

Sofia Dória (S)

Genetics Service, Department of Pathology, Faculty of Medicine, University of Porto, 4200-319 Porto, Portugal.
i3S-Instituto de Investigação e Inovação em Saúde, University of Porto, 4200-135 Porto, Portugal.

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Classifications MeSH