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Apnea of prematurity induces short and long-term development-related transcriptional changes in the murine cerebellum

Apnea of prematurity (AOP) affects more than 50% of preterm infants and leads to perinatal intermittent hypoxia (IH) which is a major cause of morbimortality worldwide. At birth, the human cerebellar cortex is still immature, making it vulnerable to perinatal events. Additionally, studies have shown...

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Autores principales: Rodriguez-Duboc, A., Basille-Dugay, M., Debonne, A., Rivière, M.-A., Vaudry, D., Burel, D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10663136/
https://www.ncbi.nlm.nih.gov/pubmed/38020806
http://dx.doi.org/10.1016/j.crneur.2023.100113
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author Rodriguez-Duboc, A.
Basille-Dugay, M.
Debonne, A.
Rivière, M.-A.
Vaudry, D.
Burel, D.
author_facet Rodriguez-Duboc, A.
Basille-Dugay, M.
Debonne, A.
Rivière, M.-A.
Vaudry, D.
Burel, D.
author_sort Rodriguez-Duboc, A.
collection PubMed
description Apnea of prematurity (AOP) affects more than 50% of preterm infants and leads to perinatal intermittent hypoxia (IH) which is a major cause of morbimortality worldwide. At birth, the human cerebellar cortex is still immature, making it vulnerable to perinatal events. Additionally, studies have shown a correlation between cerebellar functions and the deficits observed in children who have experienced AOP. Yet, the cerebellar alterations underpinning this link remain poorly understood. To gain insight into the involvement of the cerebellum in perinatal hypoxia-related consequences, we developed a mouse model of AOP. Our previous research has revealed that IH induces oxidative stress in the developing cerebellum, as evidenced by the over-expression of genes involved in reactive oxygen species production and the under-expression of genes encoding antioxidant enzymes. These changes suggest a failure of the defense system against oxidative stress and could be responsible for neuronal death in the cerebellum. Building upon these findings, we conducted a transcriptomic study of the genes involved in the processes that occur during cerebellar development. Using real-time PCR, we analyzed the expression of these genes at different developmental stages and in various cell types. This enabled us to pinpoint a timeframe of vulnerability at P8, which represents the age with the highest number of downregulated genes in the cerebellum. Furthermore, we discovered that our IH protocol affects several molecular pathways, including proliferation, migration, and differentiation. This indicates that IH can impact the development of different cell types, potentially contributing to the histological and behavioral deficits observed in this model. Overall, our data strongly suggest that the cerebellum is highly sensitive to IH, and provide valuable insights into the cellular and molecular mechanisms underlying AOP. In the long term, these findings may contribute to the identification of novel therapeutic targets for improving the clinical management of this prevalent pathology.
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spelling pubmed-106631362023-10-20 Apnea of prematurity induces short and long-term development-related transcriptional changes in the murine cerebellum Rodriguez-Duboc, A. Basille-Dugay, M. Debonne, A. Rivière, M.-A. Vaudry, D. Burel, D. Curr Res Neurobiol Research Article Apnea of prematurity (AOP) affects more than 50% of preterm infants and leads to perinatal intermittent hypoxia (IH) which is a major cause of morbimortality worldwide. At birth, the human cerebellar cortex is still immature, making it vulnerable to perinatal events. Additionally, studies have shown a correlation between cerebellar functions and the deficits observed in children who have experienced AOP. Yet, the cerebellar alterations underpinning this link remain poorly understood. To gain insight into the involvement of the cerebellum in perinatal hypoxia-related consequences, we developed a mouse model of AOP. Our previous research has revealed that IH induces oxidative stress in the developing cerebellum, as evidenced by the over-expression of genes involved in reactive oxygen species production and the under-expression of genes encoding antioxidant enzymes. These changes suggest a failure of the defense system against oxidative stress and could be responsible for neuronal death in the cerebellum. Building upon these findings, we conducted a transcriptomic study of the genes involved in the processes that occur during cerebellar development. Using real-time PCR, we analyzed the expression of these genes at different developmental stages and in various cell types. This enabled us to pinpoint a timeframe of vulnerability at P8, which represents the age with the highest number of downregulated genes in the cerebellum. Furthermore, we discovered that our IH protocol affects several molecular pathways, including proliferation, migration, and differentiation. This indicates that IH can impact the development of different cell types, potentially contributing to the histological and behavioral deficits observed in this model. Overall, our data strongly suggest that the cerebellum is highly sensitive to IH, and provide valuable insights into the cellular and molecular mechanisms underlying AOP. In the long term, these findings may contribute to the identification of novel therapeutic targets for improving the clinical management of this prevalent pathology. Elsevier 2023-10-20 /pmc/articles/PMC10663136/ /pubmed/38020806 http://dx.doi.org/10.1016/j.crneur.2023.100113 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Rodriguez-Duboc, A.
Basille-Dugay, M.
Debonne, A.
Rivière, M.-A.
Vaudry, D.
Burel, D.
Apnea of prematurity induces short and long-term development-related transcriptional changes in the murine cerebellum
title Apnea of prematurity induces short and long-term development-related transcriptional changes in the murine cerebellum
title_full Apnea of prematurity induces short and long-term development-related transcriptional changes in the murine cerebellum
title_fullStr Apnea of prematurity induces short and long-term development-related transcriptional changes in the murine cerebellum
title_full_unstemmed Apnea of prematurity induces short and long-term development-related transcriptional changes in the murine cerebellum
title_short Apnea of prematurity induces short and long-term development-related transcriptional changes in the murine cerebellum
title_sort apnea of prematurity induces short and long-term development-related transcriptional changes in the murine cerebellum
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10663136/
https://www.ncbi.nlm.nih.gov/pubmed/38020806
http://dx.doi.org/10.1016/j.crneur.2023.100113
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