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Differential effects of early or late exposure to prenatal maternal immune activation on mouse embryonic neurodevelopment
Exposure to maternal immune activation (MIA) in utero is a risk factor for neurodevelopmental and psychiatric disorders. MIA-induced deficits in adolescent and adult offspring have been well characterized; however, less is known about the effects of MIA exposure on embryo development. To address thi...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8944668/ https://www.ncbi.nlm.nih.gov/pubmed/35286203 http://dx.doi.org/10.1073/pnas.2114545119 |
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author | Guma, Elisa Bordeleau, Maude González Ibáñez, Fernando Picard, Katherine Snook, Emily Desrosiers-Grégoire, Gabriel Spring, Shoshana Lerch, Jason P. Nieman, Brian J. Devenyi, Gabriel A. Tremblay, Marie-Eve Chakravarty, M. Mallar |
author_facet | Guma, Elisa Bordeleau, Maude González Ibáñez, Fernando Picard, Katherine Snook, Emily Desrosiers-Grégoire, Gabriel Spring, Shoshana Lerch, Jason P. Nieman, Brian J. Devenyi, Gabriel A. Tremblay, Marie-Eve Chakravarty, M. Mallar |
author_sort | Guma, Elisa |
collection | PubMed |
description | Exposure to maternal immune activation (MIA) in utero is a risk factor for neurodevelopmental and psychiatric disorders. MIA-induced deficits in adolescent and adult offspring have been well characterized; however, less is known about the effects of MIA exposure on embryo development. To address this gap, we performed high-resolution ex vivo MRI to investigate the effects of early (gestational day [GD]9) and late (GD17) MIA exposure on embryo (GD18) brain structure. We identify striking neuroanatomical changes in the embryo brain, particularly in the late-exposed offspring. We further examined the putative neuroanatomical underpinnings of MIA timing in the hippocampus using electron microscopy and identified differential effects due to MIA timing. An increase in apoptotic cell density was observed in the GD9-exposed offspring, while an increase in the density of neurons and glia with ultrastructural features reflective of increased neuroinflammation and oxidative stress was observed in GD17-exposed offspring, particularly in females. Overall, our findings integrate imaging techniques across different scales to identify differential impact of MIA timing on the earliest stages of neurodevelopment. |
format | Online Article Text |
id | pubmed-8944668 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-89446682022-09-14 Differential effects of early or late exposure to prenatal maternal immune activation on mouse embryonic neurodevelopment Guma, Elisa Bordeleau, Maude González Ibáñez, Fernando Picard, Katherine Snook, Emily Desrosiers-Grégoire, Gabriel Spring, Shoshana Lerch, Jason P. Nieman, Brian J. Devenyi, Gabriel A. Tremblay, Marie-Eve Chakravarty, M. Mallar Proc Natl Acad Sci U S A Biological Sciences Exposure to maternal immune activation (MIA) in utero is a risk factor for neurodevelopmental and psychiatric disorders. MIA-induced deficits in adolescent and adult offspring have been well characterized; however, less is known about the effects of MIA exposure on embryo development. To address this gap, we performed high-resolution ex vivo MRI to investigate the effects of early (gestational day [GD]9) and late (GD17) MIA exposure on embryo (GD18) brain structure. We identify striking neuroanatomical changes in the embryo brain, particularly in the late-exposed offspring. We further examined the putative neuroanatomical underpinnings of MIA timing in the hippocampus using electron microscopy and identified differential effects due to MIA timing. An increase in apoptotic cell density was observed in the GD9-exposed offspring, while an increase in the density of neurons and glia with ultrastructural features reflective of increased neuroinflammation and oxidative stress was observed in GD17-exposed offspring, particularly in females. Overall, our findings integrate imaging techniques across different scales to identify differential impact of MIA timing on the earliest stages of neurodevelopment. National Academy of Sciences 2022-03-14 2022-03-22 /pmc/articles/PMC8944668/ /pubmed/35286203 http://dx.doi.org/10.1073/pnas.2114545119 Text en Copyright © 2022 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Biological Sciences Guma, Elisa Bordeleau, Maude González Ibáñez, Fernando Picard, Katherine Snook, Emily Desrosiers-Grégoire, Gabriel Spring, Shoshana Lerch, Jason P. Nieman, Brian J. Devenyi, Gabriel A. Tremblay, Marie-Eve Chakravarty, M. Mallar Differential effects of early or late exposure to prenatal maternal immune activation on mouse embryonic neurodevelopment |
title | Differential effects of early or late exposure to prenatal maternal immune activation on mouse embryonic neurodevelopment |
title_full | Differential effects of early or late exposure to prenatal maternal immune activation on mouse embryonic neurodevelopment |
title_fullStr | Differential effects of early or late exposure to prenatal maternal immune activation on mouse embryonic neurodevelopment |
title_full_unstemmed | Differential effects of early or late exposure to prenatal maternal immune activation on mouse embryonic neurodevelopment |
title_short | Differential effects of early or late exposure to prenatal maternal immune activation on mouse embryonic neurodevelopment |
title_sort | differential effects of early or late exposure to prenatal maternal immune activation on mouse embryonic neurodevelopment |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8944668/ https://www.ncbi.nlm.nih.gov/pubmed/35286203 http://dx.doi.org/10.1073/pnas.2114545119 |
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