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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2022
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.
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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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