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Cervical immune activation during the luteal phase may compromise subsequent trans-cervical ram sperm transport(†)

Worldwide, cervical artificial insemination using frozen–thawed semen yields low pregnancy rates. The only exception to this is in Norway, where vaginal insemination with frozen–thawed semen yields pregnancy rates in excess of 60% and which has been attributed to the specific ewe breed used. Our pre...

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Autores principales: Abril-Parreño, Laura, Krogenæs, Anette Kristine, Druart, Xavier, Cormican, Paul, Fair, Sean, Meade, Kieran G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9562110/
https://www.ncbi.nlm.nih.gov/pubmed/35766421
http://dx.doi.org/10.1093/biolre/ioac130
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author Abril-Parreño, Laura
Krogenæs, Anette Kristine
Druart, Xavier
Cormican, Paul
Fair, Sean
Meade, Kieran G
author_facet Abril-Parreño, Laura
Krogenæs, Anette Kristine
Druart, Xavier
Cormican, Paul
Fair, Sean
Meade, Kieran G
author_sort Abril-Parreño, Laura
collection PubMed
description Worldwide, cervical artificial insemination using frozen–thawed semen yields low pregnancy rates. The only exception to this is in Norway, where vaginal insemination with frozen–thawed semen yields pregnancy rates in excess of 60% and which has been attributed to the specific ewe breed used. Our previous work demonstrated differences in cervical gene expression at the follicular phase of the estrous cycle in ewe breeds with known differences in pregnancy rates. In this study, we characterized the cervical transcriptome of the same ewe breeds [Suffolk, Belclare, Fur, and Norwegian White Sheep (NWS)] during the luteal phase, as an optimal environment at the luteal phase could better prepare the cervix for sperm migration through the cervix at the subsequent follicular phase. High-quality RNA extracted from postmortem cervical tissue was analyzed by RNA sequencing. After stringent filtering, 1051, 1924, and 611 differentially expressed genes (DEGs) were detected in the low-fertility Suffolk breed compared with Belclare, Fur, and NWS, respectively. Gene ontology analysis identified increased humoral adaptive immune response pathways in Suffolk. Increased expression of multiple immune genes supports the presence of an active immune response in the cervix of Suffolk ewes, which differentiates them significantly from the other three ewe breeds. Inflammatory pathways were upregulated in the Suffolk, resulting in higher expression of the potent pro-inflammatory cytokines. Therefore, higher levels of pro-inflammatory cytokines indicate unresolved inflammation in the cervix of the low-fertility Suffolk breed that could contribute to reduced cervical sperm transport in the next follicular phase.
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spelling pubmed-95621102022-10-18 Cervical immune activation during the luteal phase may compromise subsequent trans-cervical ram sperm transport(†) Abril-Parreño, Laura Krogenæs, Anette Kristine Druart, Xavier Cormican, Paul Fair, Sean Meade, Kieran G Biol Reprod Research Article Worldwide, cervical artificial insemination using frozen–thawed semen yields low pregnancy rates. The only exception to this is in Norway, where vaginal insemination with frozen–thawed semen yields pregnancy rates in excess of 60% and which has been attributed to the specific ewe breed used. Our previous work demonstrated differences in cervical gene expression at the follicular phase of the estrous cycle in ewe breeds with known differences in pregnancy rates. In this study, we characterized the cervical transcriptome of the same ewe breeds [Suffolk, Belclare, Fur, and Norwegian White Sheep (NWS)] during the luteal phase, as an optimal environment at the luteal phase could better prepare the cervix for sperm migration through the cervix at the subsequent follicular phase. High-quality RNA extracted from postmortem cervical tissue was analyzed by RNA sequencing. After stringent filtering, 1051, 1924, and 611 differentially expressed genes (DEGs) were detected in the low-fertility Suffolk breed compared with Belclare, Fur, and NWS, respectively. Gene ontology analysis identified increased humoral adaptive immune response pathways in Suffolk. Increased expression of multiple immune genes supports the presence of an active immune response in the cervix of Suffolk ewes, which differentiates them significantly from the other three ewe breeds. Inflammatory pathways were upregulated in the Suffolk, resulting in higher expression of the potent pro-inflammatory cytokines. Therefore, higher levels of pro-inflammatory cytokines indicate unresolved inflammation in the cervix of the low-fertility Suffolk breed that could contribute to reduced cervical sperm transport in the next follicular phase. Oxford University Press 2022-06-29 /pmc/articles/PMC9562110/ /pubmed/35766421 http://dx.doi.org/10.1093/biolre/ioac130 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Society for the Study of Reproduction. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Research Article
Abril-Parreño, Laura
Krogenæs, Anette Kristine
Druart, Xavier
Cormican, Paul
Fair, Sean
Meade, Kieran G
Cervical immune activation during the luteal phase may compromise subsequent trans-cervical ram sperm transport(†)
title Cervical immune activation during the luteal phase may compromise subsequent trans-cervical ram sperm transport(†)
title_full Cervical immune activation during the luteal phase may compromise subsequent trans-cervical ram sperm transport(†)
title_fullStr Cervical immune activation during the luteal phase may compromise subsequent trans-cervical ram sperm transport(†)
title_full_unstemmed Cervical immune activation during the luteal phase may compromise subsequent trans-cervical ram sperm transport(†)
title_short Cervical immune activation during the luteal phase may compromise subsequent trans-cervical ram sperm transport(†)
title_sort cervical immune activation during the luteal phase may compromise subsequent trans-cervical ram sperm transport(†)
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9562110/
https://www.ncbi.nlm.nih.gov/pubmed/35766421
http://dx.doi.org/10.1093/biolre/ioac130
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