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Preimplantation factor is an anti-apoptotic effector in human trophoblasts involving p53 signaling pathway

From the earliest stages of gestation, embryonic–maternal interaction has a key role in a successful pregnancy. Various factors present during gestation may significantly influence this type of juxta/paracrine interaction. PreImplantation Factor (PIF) is a recently identified factor with activity at...

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Autores principales: Moindjie, Hadia, Santos, Esther Dos, Gouesse, Rita-Josiane, Swierkowski-Blanchard, Nelly, Serazin, Valérie, Barnea, Eytan R, Vialard, François, Dieudonné, Marie-Noëlle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5261002/
https://www.ncbi.nlm.nih.gov/pubmed/27906186
http://dx.doi.org/10.1038/cddis.2016.382
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author Moindjie, Hadia
Santos, Esther Dos
Gouesse, Rita-Josiane
Swierkowski-Blanchard, Nelly
Serazin, Valérie
Barnea, Eytan R
Vialard, François
Dieudonné, Marie-Noëlle
author_facet Moindjie, Hadia
Santos, Esther Dos
Gouesse, Rita-Josiane
Swierkowski-Blanchard, Nelly
Serazin, Valérie
Barnea, Eytan R
Vialard, François
Dieudonné, Marie-Noëlle
author_sort Moindjie, Hadia
collection PubMed
description From the earliest stages of gestation, embryonic–maternal interaction has a key role in a successful pregnancy. Various factors present during gestation may significantly influence this type of juxta/paracrine interaction. PreImplantation Factor (PIF) is a recently identified factor with activity at the fetomaternal interface. PIF is secreted by viable embryos and directly controls placental development by increasing the invasive capacity of human extravillous trophoblasts (EVTs). To further specify PIF's role in the human placenta, we analyzed the genome-wide expression profile of the EVT in the presence of a synthetic PIF analog (sPIF). We found that sPIF exposure altered several pathways related to p53 signaling, survival and the immune response. Functional assays revealed that sPIF acts through the p53 pathway to reduce both early and late trophoblast apoptosis. More precisely, sPIF (i) decreases the phosphorylation of p53 at Ser-15, (ii) enhances the B-cell lymphoma-2 (BCL2) expression and (iii) reduces the BCL2-associated X protein (BAX) and BCL2 homologous antagonist killer (BAK) mRNA expression levels. Furthermore, invalidation experiments of TP53 allowed us to demonstrate that PIF's effects on placental apoptosis seemed to be essentially mediated by this gene. We have clearly shown that p53 and sPIF pathways could interact in human trophoblast and thus promotes cell survival. Furthermore, sPIF was found to regulate a gene network related to immune tolerance in the EVT, which emphasizes the beneficial effect of this peptide on the human placenta. Finally, the PIF protein levels in placentas from pregnancies affected by preeclampsia or intra-uterine growth restriction were significantly lower than in gestational age-matched control placentas. Taken as a whole, our results suggest that sPIF protects the EVT's functional status through a variety of mechanisms. Clinical application of sPIF in the treatment of disorders of early pregnancy can be envisioned.
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spelling pubmed-52610022017-01-26 Preimplantation factor is an anti-apoptotic effector in human trophoblasts involving p53 signaling pathway Moindjie, Hadia Santos, Esther Dos Gouesse, Rita-Josiane Swierkowski-Blanchard, Nelly Serazin, Valérie Barnea, Eytan R Vialard, François Dieudonné, Marie-Noëlle Cell Death Dis Original Article From the earliest stages of gestation, embryonic–maternal interaction has a key role in a successful pregnancy. Various factors present during gestation may significantly influence this type of juxta/paracrine interaction. PreImplantation Factor (PIF) is a recently identified factor with activity at the fetomaternal interface. PIF is secreted by viable embryos and directly controls placental development by increasing the invasive capacity of human extravillous trophoblasts (EVTs). To further specify PIF's role in the human placenta, we analyzed the genome-wide expression profile of the EVT in the presence of a synthetic PIF analog (sPIF). We found that sPIF exposure altered several pathways related to p53 signaling, survival and the immune response. Functional assays revealed that sPIF acts through the p53 pathway to reduce both early and late trophoblast apoptosis. More precisely, sPIF (i) decreases the phosphorylation of p53 at Ser-15, (ii) enhances the B-cell lymphoma-2 (BCL2) expression and (iii) reduces the BCL2-associated X protein (BAX) and BCL2 homologous antagonist killer (BAK) mRNA expression levels. Furthermore, invalidation experiments of TP53 allowed us to demonstrate that PIF's effects on placental apoptosis seemed to be essentially mediated by this gene. We have clearly shown that p53 and sPIF pathways could interact in human trophoblast and thus promotes cell survival. Furthermore, sPIF was found to regulate a gene network related to immune tolerance in the EVT, which emphasizes the beneficial effect of this peptide on the human placenta. Finally, the PIF protein levels in placentas from pregnancies affected by preeclampsia or intra-uterine growth restriction were significantly lower than in gestational age-matched control placentas. Taken as a whole, our results suggest that sPIF protects the EVT's functional status through a variety of mechanisms. Clinical application of sPIF in the treatment of disorders of early pregnancy can be envisioned. Nature Publishing Group 2016-12 2016-12-01 /pmc/articles/PMC5261002/ /pubmed/27906186 http://dx.doi.org/10.1038/cddis.2016.382 Text en Copyright © 2016 The Author(s) http://creativecommons.org/licenses/by/4.0/ Cell Death and Disease is an open-access journal published by Nature Publishing Group. This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Original Article
Moindjie, Hadia
Santos, Esther Dos
Gouesse, Rita-Josiane
Swierkowski-Blanchard, Nelly
Serazin, Valérie
Barnea, Eytan R
Vialard, François
Dieudonné, Marie-Noëlle
Preimplantation factor is an anti-apoptotic effector in human trophoblasts involving p53 signaling pathway
title Preimplantation factor is an anti-apoptotic effector in human trophoblasts involving p53 signaling pathway
title_full Preimplantation factor is an anti-apoptotic effector in human trophoblasts involving p53 signaling pathway
title_fullStr Preimplantation factor is an anti-apoptotic effector in human trophoblasts involving p53 signaling pathway
title_full_unstemmed Preimplantation factor is an anti-apoptotic effector in human trophoblasts involving p53 signaling pathway
title_short Preimplantation factor is an anti-apoptotic effector in human trophoblasts involving p53 signaling pathway
title_sort preimplantation factor is an anti-apoptotic effector in human trophoblasts involving p53 signaling pathway
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5261002/
https://www.ncbi.nlm.nih.gov/pubmed/27906186
http://dx.doi.org/10.1038/cddis.2016.382
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