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Dynamic miRNA changes during the process of epileptogenesis in an infantile and adult-onset model

Temporal lobe epilepsy (TLE) is the most common epilepsy type. TLE onset in infancy aggravates features like severity, drug responsiveness, or development of comorbidities. These aggravations may arise from altered micro RNA (miRNA) expression specific to the early onset of the disease. Although the...

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Autores principales: Bencurova, Petra, Baloun, Jiri, Hynst, Jakub, Oppelt, Jan, Kubova, Hana, Pospisilova, Sarka, Brazdil, Milan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8102630/
https://www.ncbi.nlm.nih.gov/pubmed/33958654
http://dx.doi.org/10.1038/s41598-021-89084-9
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author Bencurova, Petra
Baloun, Jiri
Hynst, Jakub
Oppelt, Jan
Kubova, Hana
Pospisilova, Sarka
Brazdil, Milan
author_facet Bencurova, Petra
Baloun, Jiri
Hynst, Jakub
Oppelt, Jan
Kubova, Hana
Pospisilova, Sarka
Brazdil, Milan
author_sort Bencurova, Petra
collection PubMed
description Temporal lobe epilepsy (TLE) is the most common epilepsy type. TLE onset in infancy aggravates features like severity, drug responsiveness, or development of comorbidities. These aggravations may arise from altered micro RNA (miRNA) expression specific to the early onset of the disease. Although the miRNA involvement in TLE is widely studied, the relationship between the onset-age and miRNA expression has not been addressed. Here, we investigated the miRNA profile of infantile and adult-onset TLE in rats combining sequencing and PCR. Since miRNA expression changes with the disease progression, we scrutinized miRNA dynamics across three stages: acute, latent, and chronic. We report that infantile-onset TLE leads to changes in the expression of fewer miRNAs across these stages. Interestingly, the miRNA profile in the acute stage of infantile-onset TLE overlaps in dysregulation of miR-132-5p, -205, and -211-3p with the chronic stage of the disease starting in adulthood. The analysis of putative targets linked the majority of dysregulated miRNAs with pathways involved in epilepsy. Our profiling uncovered miRNA expression characteristic for infantile and adulthood-onset epileptogenesis, suggesting the distinct biology underlying TLE in the onset age-dependent matter. Our results indicate the necessity of addressing the onset age as an important parameter in future epilepsy research.
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spelling pubmed-81026302021-05-10 Dynamic miRNA changes during the process of epileptogenesis in an infantile and adult-onset model Bencurova, Petra Baloun, Jiri Hynst, Jakub Oppelt, Jan Kubova, Hana Pospisilova, Sarka Brazdil, Milan Sci Rep Article Temporal lobe epilepsy (TLE) is the most common epilepsy type. TLE onset in infancy aggravates features like severity, drug responsiveness, or development of comorbidities. These aggravations may arise from altered micro RNA (miRNA) expression specific to the early onset of the disease. Although the miRNA involvement in TLE is widely studied, the relationship between the onset-age and miRNA expression has not been addressed. Here, we investigated the miRNA profile of infantile and adult-onset TLE in rats combining sequencing and PCR. Since miRNA expression changes with the disease progression, we scrutinized miRNA dynamics across three stages: acute, latent, and chronic. We report that infantile-onset TLE leads to changes in the expression of fewer miRNAs across these stages. Interestingly, the miRNA profile in the acute stage of infantile-onset TLE overlaps in dysregulation of miR-132-5p, -205, and -211-3p with the chronic stage of the disease starting in adulthood. The analysis of putative targets linked the majority of dysregulated miRNAs with pathways involved in epilepsy. Our profiling uncovered miRNA expression characteristic for infantile and adulthood-onset epileptogenesis, suggesting the distinct biology underlying TLE in the onset age-dependent matter. Our results indicate the necessity of addressing the onset age as an important parameter in future epilepsy research. Nature Publishing Group UK 2021-05-06 /pmc/articles/PMC8102630/ /pubmed/33958654 http://dx.doi.org/10.1038/s41598-021-89084-9 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This 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 Article
Bencurova, Petra
Baloun, Jiri
Hynst, Jakub
Oppelt, Jan
Kubova, Hana
Pospisilova, Sarka
Brazdil, Milan
Dynamic miRNA changes during the process of epileptogenesis in an infantile and adult-onset model
title Dynamic miRNA changes during the process of epileptogenesis in an infantile and adult-onset model
title_full Dynamic miRNA changes during the process of epileptogenesis in an infantile and adult-onset model
title_fullStr Dynamic miRNA changes during the process of epileptogenesis in an infantile and adult-onset model
title_full_unstemmed Dynamic miRNA changes during the process of epileptogenesis in an infantile and adult-onset model
title_short Dynamic miRNA changes during the process of epileptogenesis in an infantile and adult-onset model
title_sort dynamic mirna changes during the process of epileptogenesis in an infantile and adult-onset model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8102630/
https://www.ncbi.nlm.nih.gov/pubmed/33958654
http://dx.doi.org/10.1038/s41598-021-89084-9
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