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Androgens Upregulate Pathogen-Induced Placental Innate Immune Response

Group B Streptococcus (GBS) is a leading cause of placental infection, termed chorioamnionitis. Chorioamnionitis is associated with an increased risk of neurobehavioral impairments, such as autism spectrum disorders, which are more prominent in males than in female offspring. In a pre-clinical model...

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Autores principales: Vancolen, Seline, Ayash, Taghreed, Segura, Mariela, Allard, Marie-Julie, Robaire, Bernard, Sébire, Guillaume
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9104209/
https://www.ncbi.nlm.nih.gov/pubmed/35563368
http://dx.doi.org/10.3390/ijms23094978
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author Vancolen, Seline
Ayash, Taghreed
Segura, Mariela
Allard, Marie-Julie
Robaire, Bernard
Sébire, Guillaume
author_facet Vancolen, Seline
Ayash, Taghreed
Segura, Mariela
Allard, Marie-Julie
Robaire, Bernard
Sébire, Guillaume
author_sort Vancolen, Seline
collection PubMed
description Group B Streptococcus (GBS) is a leading cause of placental infection, termed chorioamnionitis. Chorioamnionitis is associated with an increased risk of neurobehavioral impairments, such as autism spectrum disorders, which are more prominent in males than in female offspring. In a pre-clinical model of chorioamnionitis, a greater inflammatory response was observed in placenta associated with male rather than female fetuses, correlating with the severity of subsequent neurobehavioral impairments. The reason for this sex difference is not understood. Our hypothesis is that androgens upregulate the placental innate immune response in male fetuses. Lewis dams were injected daily from gestational day (G) 18 to 21 with corn oil (vehicle) or an androgen receptor antagonist (flutamide). On G 19, dams were injected with saline (control) or GBS. Maternal, fetal sera and placentas were collected for protein assays and in situ analyses. Our results showed that while flutamide alone had no effect, a decrease in placental concentration of pro-inflammatory cytokines and infiltration of polymorphonuclear cells was observed in flutamide/infected compared to vehicle/infected groups. These results show that androgens upregulate the placental innate immune response and thus may contribute to the skewed sex ratio towards males observed in several developmental impairments resulting from perinatal infection/inflammation.
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spelling pubmed-91042092022-05-14 Androgens Upregulate Pathogen-Induced Placental Innate Immune Response Vancolen, Seline Ayash, Taghreed Segura, Mariela Allard, Marie-Julie Robaire, Bernard Sébire, Guillaume Int J Mol Sci Article Group B Streptococcus (GBS) is a leading cause of placental infection, termed chorioamnionitis. Chorioamnionitis is associated with an increased risk of neurobehavioral impairments, such as autism spectrum disorders, which are more prominent in males than in female offspring. In a pre-clinical model of chorioamnionitis, a greater inflammatory response was observed in placenta associated with male rather than female fetuses, correlating with the severity of subsequent neurobehavioral impairments. The reason for this sex difference is not understood. Our hypothesis is that androgens upregulate the placental innate immune response in male fetuses. Lewis dams were injected daily from gestational day (G) 18 to 21 with corn oil (vehicle) or an androgen receptor antagonist (flutamide). On G 19, dams were injected with saline (control) or GBS. Maternal, fetal sera and placentas were collected for protein assays and in situ analyses. Our results showed that while flutamide alone had no effect, a decrease in placental concentration of pro-inflammatory cytokines and infiltration of polymorphonuclear cells was observed in flutamide/infected compared to vehicle/infected groups. These results show that androgens upregulate the placental innate immune response and thus may contribute to the skewed sex ratio towards males observed in several developmental impairments resulting from perinatal infection/inflammation. MDPI 2022-04-29 /pmc/articles/PMC9104209/ /pubmed/35563368 http://dx.doi.org/10.3390/ijms23094978 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Vancolen, Seline
Ayash, Taghreed
Segura, Mariela
Allard, Marie-Julie
Robaire, Bernard
Sébire, Guillaume
Androgens Upregulate Pathogen-Induced Placental Innate Immune Response
title Androgens Upregulate Pathogen-Induced Placental Innate Immune Response
title_full Androgens Upregulate Pathogen-Induced Placental Innate Immune Response
title_fullStr Androgens Upregulate Pathogen-Induced Placental Innate Immune Response
title_full_unstemmed Androgens Upregulate Pathogen-Induced Placental Innate Immune Response
title_short Androgens Upregulate Pathogen-Induced Placental Innate Immune Response
title_sort androgens upregulate pathogen-induced placental innate immune response
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9104209/
https://www.ncbi.nlm.nih.gov/pubmed/35563368
http://dx.doi.org/10.3390/ijms23094978
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