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Sex-Specific Differences in the Placental Unfolded Protein Response in a Rodent Model of Gestational Hypoxia

Gestational hypoxia is a major contributor to fetal growth restriction (FGR) and perinatal morbidity and mortality and has been closely linked to the activation of the unfolded protein response (UPR) in the placenta. Recent studies on adverse pregnancy conditions show differential adaptive responses...

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Autores principales: Tong, Wen, Ganguly, Esha, Villalobos-Labra, Roberto, Quon, Anita, Spaans, Floor, Giussani, Dino A., Davidge, Sandra T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10229681/
https://www.ncbi.nlm.nih.gov/pubmed/36574145
http://dx.doi.org/10.1007/s43032-022-01157-w
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author Tong, Wen
Ganguly, Esha
Villalobos-Labra, Roberto
Quon, Anita
Spaans, Floor
Giussani, Dino A.
Davidge, Sandra T.
author_facet Tong, Wen
Ganguly, Esha
Villalobos-Labra, Roberto
Quon, Anita
Spaans, Floor
Giussani, Dino A.
Davidge, Sandra T.
author_sort Tong, Wen
collection PubMed
description Gestational hypoxia is a major contributor to fetal growth restriction (FGR) and perinatal morbidity and mortality and has been closely linked to the activation of the unfolded protein response (UPR) in the placenta. Recent studies on adverse pregnancy conditions show differential adaptive responses in pregnancies carrying male or female fetuses. Here, we use an established rat model of hypoxic pregnancy and FGR to test the hypothesis that chronic hypoxia promotes sexually dimorphic activation of the placental UPR. Our data showed that gestational hypoxia increased glucose regulatory protein 78 (GRP78) expression in male placentae, increased activating transcription factor 6 activation (ATF6) in female placentae, and did not induce changes in other UPR markers. In addition, gestational hypoxia reduced fetal weight only in males and ATF6 activation correlated with an increase in the fetal crown-rump-length/body weight ratio only in females. These results suggest sex-specific divergence in the placental adaptive response to gestational hypoxia, which may account for the sexual dimorphism observed in placental function and pregnancy outcomes in complicated pregnancies. GRAPHICAL ABSTRACT: [Image: see text]
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spelling pubmed-102296812023-06-01 Sex-Specific Differences in the Placental Unfolded Protein Response in a Rodent Model of Gestational Hypoxia Tong, Wen Ganguly, Esha Villalobos-Labra, Roberto Quon, Anita Spaans, Floor Giussani, Dino A. Davidge, Sandra T. Reprod Sci Pregnancy: Short Communications Gestational hypoxia is a major contributor to fetal growth restriction (FGR) and perinatal morbidity and mortality and has been closely linked to the activation of the unfolded protein response (UPR) in the placenta. Recent studies on adverse pregnancy conditions show differential adaptive responses in pregnancies carrying male or female fetuses. Here, we use an established rat model of hypoxic pregnancy and FGR to test the hypothesis that chronic hypoxia promotes sexually dimorphic activation of the placental UPR. Our data showed that gestational hypoxia increased glucose regulatory protein 78 (GRP78) expression in male placentae, increased activating transcription factor 6 activation (ATF6) in female placentae, and did not induce changes in other UPR markers. In addition, gestational hypoxia reduced fetal weight only in males and ATF6 activation correlated with an increase in the fetal crown-rump-length/body weight ratio only in females. These results suggest sex-specific divergence in the placental adaptive response to gestational hypoxia, which may account for the sexual dimorphism observed in placental function and pregnancy outcomes in complicated pregnancies. GRAPHICAL ABSTRACT: [Image: see text] Springer International Publishing 2022-12-27 /pmc/articles/PMC10229681/ /pubmed/36574145 http://dx.doi.org/10.1007/s43032-022-01157-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Pregnancy: Short Communications
Tong, Wen
Ganguly, Esha
Villalobos-Labra, Roberto
Quon, Anita
Spaans, Floor
Giussani, Dino A.
Davidge, Sandra T.
Sex-Specific Differences in the Placental Unfolded Protein Response in a Rodent Model of Gestational Hypoxia
title Sex-Specific Differences in the Placental Unfolded Protein Response in a Rodent Model of Gestational Hypoxia
title_full Sex-Specific Differences in the Placental Unfolded Protein Response in a Rodent Model of Gestational Hypoxia
title_fullStr Sex-Specific Differences in the Placental Unfolded Protein Response in a Rodent Model of Gestational Hypoxia
title_full_unstemmed Sex-Specific Differences in the Placental Unfolded Protein Response in a Rodent Model of Gestational Hypoxia
title_short Sex-Specific Differences in the Placental Unfolded Protein Response in a Rodent Model of Gestational Hypoxia
title_sort sex-specific differences in the placental unfolded protein response in a rodent model of gestational hypoxia
topic Pregnancy: Short Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10229681/
https://www.ncbi.nlm.nih.gov/pubmed/36574145
http://dx.doi.org/10.1007/s43032-022-01157-w
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