Cargando…

Pre-hatching embryo-dependent and -independent programming of endometrial function in cattle

The bovine pre-implantation embryo secretes bioactive molecules from early development stages, but effects on endometrial function are reported to start only after elongation. Here, we interrogated spatially defined regions of the endometrium transcriptome for responses to a day 7 embryo in vivo. We...

Descripción completa

Detalles Bibliográficos
Autores principales: Sponchiado, Mariana, Gomes, Nathália Souza, Fontes, Patrícia Kubo, Martins, Thiago, del Collado, Maite, Pastore, Athos de Assumpção, Pugliesi, Guilherme, Nogueira, Marcelo Fábio Gouveia, Binelli, Mario
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5397052/
https://www.ncbi.nlm.nih.gov/pubmed/28423001
http://dx.doi.org/10.1371/journal.pone.0175954
_version_ 1783230193593221120
author Sponchiado, Mariana
Gomes, Nathália Souza
Fontes, Patrícia Kubo
Martins, Thiago
del Collado, Maite
Pastore, Athos de Assumpção
Pugliesi, Guilherme
Nogueira, Marcelo Fábio Gouveia
Binelli, Mario
author_facet Sponchiado, Mariana
Gomes, Nathália Souza
Fontes, Patrícia Kubo
Martins, Thiago
del Collado, Maite
Pastore, Athos de Assumpção
Pugliesi, Guilherme
Nogueira, Marcelo Fábio Gouveia
Binelli, Mario
author_sort Sponchiado, Mariana
collection PubMed
description The bovine pre-implantation embryo secretes bioactive molecules from early development stages, but effects on endometrial function are reported to start only after elongation. Here, we interrogated spatially defined regions of the endometrium transcriptome for responses to a day 7 embryo in vivo. We hypothesize that exposure to an embryo changes the abundance of specific transcripts in the cranial region of the pregnant uterine horn. Endometrium was collected from the uterotubal junction (UTJ), anterior (IA), medial (IM) and posterior (IP) regions of the uterine horn ipsilateral to the CL 7 days after estrus from sham-inseminated (Con) or artificially inseminated, confirmed pregnant (Preg) cows. Abundance of 86 transcripts was evaluated by qPCR using a microfluidic platform. Abundance of 12 transcripts was modulated in the Preg endometrium, including classical interferon-stimulated genes (ISG15, MX1, MX2 and OAS1Y), prostaglandin biosynthesis genes (PTGES, HPGD and AKR1C4), water channel (AQP4) and a solute transporter (SLC1A4) and this was in the UTJ and IA mainly. Additionally, for 71 transcripts, abundance varied according to region of the reproductive tract. Regulation included downregulation of genes associated with proliferation (IGF1, IGF2, IGF1R and IGF2R) and extracellular matrix remodeling (MMP14, MMP19 and MMP2) and upregulation of anti-adhesive genes (MUC1) in the cranial regions of uterine horn. Physical proximity to the embryo provides paracrine regulation of endometrial function. Embryo-independent regulation of the endometrial transcriptome may support subsequent stages of embryo development, such as elongation and implantation. We speculate that successful early embryo-dependent and -independent programming fine-tune endometrial functions that are important for maintenance of pregnancy in cattle.
format Online
Article
Text
id pubmed-5397052
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-53970522017-05-04 Pre-hatching embryo-dependent and -independent programming of endometrial function in cattle Sponchiado, Mariana Gomes, Nathália Souza Fontes, Patrícia Kubo Martins, Thiago del Collado, Maite Pastore, Athos de Assumpção Pugliesi, Guilherme Nogueira, Marcelo Fábio Gouveia Binelli, Mario PLoS One Research Article The bovine pre-implantation embryo secretes bioactive molecules from early development stages, but effects on endometrial function are reported to start only after elongation. Here, we interrogated spatially defined regions of the endometrium transcriptome for responses to a day 7 embryo in vivo. We hypothesize that exposure to an embryo changes the abundance of specific transcripts in the cranial region of the pregnant uterine horn. Endometrium was collected from the uterotubal junction (UTJ), anterior (IA), medial (IM) and posterior (IP) regions of the uterine horn ipsilateral to the CL 7 days after estrus from sham-inseminated (Con) or artificially inseminated, confirmed pregnant (Preg) cows. Abundance of 86 transcripts was evaluated by qPCR using a microfluidic platform. Abundance of 12 transcripts was modulated in the Preg endometrium, including classical interferon-stimulated genes (ISG15, MX1, MX2 and OAS1Y), prostaglandin biosynthesis genes (PTGES, HPGD and AKR1C4), water channel (AQP4) and a solute transporter (SLC1A4) and this was in the UTJ and IA mainly. Additionally, for 71 transcripts, abundance varied according to region of the reproductive tract. Regulation included downregulation of genes associated with proliferation (IGF1, IGF2, IGF1R and IGF2R) and extracellular matrix remodeling (MMP14, MMP19 and MMP2) and upregulation of anti-adhesive genes (MUC1) in the cranial regions of uterine horn. Physical proximity to the embryo provides paracrine regulation of endometrial function. Embryo-independent regulation of the endometrial transcriptome may support subsequent stages of embryo development, such as elongation and implantation. We speculate that successful early embryo-dependent and -independent programming fine-tune endometrial functions that are important for maintenance of pregnancy in cattle. Public Library of Science 2017-04-19 /pmc/articles/PMC5397052/ /pubmed/28423001 http://dx.doi.org/10.1371/journal.pone.0175954 Text en © 2017 Sponchiado et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Sponchiado, Mariana
Gomes, Nathália Souza
Fontes, Patrícia Kubo
Martins, Thiago
del Collado, Maite
Pastore, Athos de Assumpção
Pugliesi, Guilherme
Nogueira, Marcelo Fábio Gouveia
Binelli, Mario
Pre-hatching embryo-dependent and -independent programming of endometrial function in cattle
title Pre-hatching embryo-dependent and -independent programming of endometrial function in cattle
title_full Pre-hatching embryo-dependent and -independent programming of endometrial function in cattle
title_fullStr Pre-hatching embryo-dependent and -independent programming of endometrial function in cattle
title_full_unstemmed Pre-hatching embryo-dependent and -independent programming of endometrial function in cattle
title_short Pre-hatching embryo-dependent and -independent programming of endometrial function in cattle
title_sort pre-hatching embryo-dependent and -independent programming of endometrial function in cattle
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5397052/
https://www.ncbi.nlm.nih.gov/pubmed/28423001
http://dx.doi.org/10.1371/journal.pone.0175954
work_keys_str_mv AT sponchiadomariana prehatchingembryodependentandindependentprogrammingofendometrialfunctionincattle
AT gomesnathaliasouza prehatchingembryodependentandindependentprogrammingofendometrialfunctionincattle
AT fontespatriciakubo prehatchingembryodependentandindependentprogrammingofendometrialfunctionincattle
AT martinsthiago prehatchingembryodependentandindependentprogrammingofendometrialfunctionincattle
AT delcolladomaite prehatchingembryodependentandindependentprogrammingofendometrialfunctionincattle
AT pastoreathosdeassumpcao prehatchingembryodependentandindependentprogrammingofendometrialfunctionincattle
AT pugliesiguilherme prehatchingembryodependentandindependentprogrammingofendometrialfunctionincattle
AT nogueiramarcelofabiogouveia prehatchingembryodependentandindependentprogrammingofendometrialfunctionincattle
AT binellimario prehatchingembryodependentandindependentprogrammingofendometrialfunctionincattle