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Downregulation of the Astroglial Connexin Expression and Neurodegeneration after Pilocarpine-Induced Status Epilepticus

Astrocytic networks and gap junctional communication mediated by connexins (Cxs) have been repeatedly implicated in seizures, epileptogenesis, and epilepsy. However, the effect of seizures on Cx expression is controversial. The present study focused on the response of Cxs to status epilepticus (SE),...

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Autores principales: Andrioli, Anna, Fabene, Paolo Francesco, Mudò, Giuseppa, Barresi, Vincenza, Di Liberto, Valentina, Frinchi, Monica, Bentivoglio, Marina, Condorelli, Daniele Filippo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9819917/
https://www.ncbi.nlm.nih.gov/pubmed/36613467
http://dx.doi.org/10.3390/ijms24010023
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author Andrioli, Anna
Fabene, Paolo Francesco
Mudò, Giuseppa
Barresi, Vincenza
Di Liberto, Valentina
Frinchi, Monica
Bentivoglio, Marina
Condorelli, Daniele Filippo
author_facet Andrioli, Anna
Fabene, Paolo Francesco
Mudò, Giuseppa
Barresi, Vincenza
Di Liberto, Valentina
Frinchi, Monica
Bentivoglio, Marina
Condorelli, Daniele Filippo
author_sort Andrioli, Anna
collection PubMed
description Astrocytic networks and gap junctional communication mediated by connexins (Cxs) have been repeatedly implicated in seizures, epileptogenesis, and epilepsy. However, the effect of seizures on Cx expression is controversial. The present study focused on the response of Cxs to status epilepticus (SE), which is in turn an epileptogenic insult. The expression of neuronal Cx36 and astrocytic Cx30 and Cx43 mRNAs was investigated in the brain of rats in the first day after pilocarpine-induced SE. In situ hybridization revealed a progressive decrease in Cx43 and Cx30 mRNA levels, significantly marked 24 h after SE onset in neocortical areas and the hippocampus, and in most thalamic domains, whereas Cx36 mRNA did not exhibit obvious changes. Regional evaluation with quantitative real-time-RT-PCR confirmed Cx43 and Cx30 mRNA downregulation 24 h after SE, when ongoing neuronal cell death was found in the same brain regions. Immunolabeling showed at the same time point marked a decrease in Cx43, microglia activation, and interleukin-1β induction in some microglial cells. The data showed a transient downregulation of astroglial Cxs in the cortical and thalamic areas in which SE triggers neurodegenerative events in concomitance with microglia activation and cytokine expression. This could potentially represent a protective response of neuroglial networks to SE-induced acute damage.
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spelling pubmed-98199172023-01-07 Downregulation of the Astroglial Connexin Expression and Neurodegeneration after Pilocarpine-Induced Status Epilepticus Andrioli, Anna Fabene, Paolo Francesco Mudò, Giuseppa Barresi, Vincenza Di Liberto, Valentina Frinchi, Monica Bentivoglio, Marina Condorelli, Daniele Filippo Int J Mol Sci Article Astrocytic networks and gap junctional communication mediated by connexins (Cxs) have been repeatedly implicated in seizures, epileptogenesis, and epilepsy. However, the effect of seizures on Cx expression is controversial. The present study focused on the response of Cxs to status epilepticus (SE), which is in turn an epileptogenic insult. The expression of neuronal Cx36 and astrocytic Cx30 and Cx43 mRNAs was investigated in the brain of rats in the first day after pilocarpine-induced SE. In situ hybridization revealed a progressive decrease in Cx43 and Cx30 mRNA levels, significantly marked 24 h after SE onset in neocortical areas and the hippocampus, and in most thalamic domains, whereas Cx36 mRNA did not exhibit obvious changes. Regional evaluation with quantitative real-time-RT-PCR confirmed Cx43 and Cx30 mRNA downregulation 24 h after SE, when ongoing neuronal cell death was found in the same brain regions. Immunolabeling showed at the same time point marked a decrease in Cx43, microglia activation, and interleukin-1β induction in some microglial cells. The data showed a transient downregulation of astroglial Cxs in the cortical and thalamic areas in which SE triggers neurodegenerative events in concomitance with microglia activation and cytokine expression. This could potentially represent a protective response of neuroglial networks to SE-induced acute damage. MDPI 2022-12-20 /pmc/articles/PMC9819917/ /pubmed/36613467 http://dx.doi.org/10.3390/ijms24010023 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
Andrioli, Anna
Fabene, Paolo Francesco
Mudò, Giuseppa
Barresi, Vincenza
Di Liberto, Valentina
Frinchi, Monica
Bentivoglio, Marina
Condorelli, Daniele Filippo
Downregulation of the Astroglial Connexin Expression and Neurodegeneration after Pilocarpine-Induced Status Epilepticus
title Downregulation of the Astroglial Connexin Expression and Neurodegeneration after Pilocarpine-Induced Status Epilepticus
title_full Downregulation of the Astroglial Connexin Expression and Neurodegeneration after Pilocarpine-Induced Status Epilepticus
title_fullStr Downregulation of the Astroglial Connexin Expression and Neurodegeneration after Pilocarpine-Induced Status Epilepticus
title_full_unstemmed Downregulation of the Astroglial Connexin Expression and Neurodegeneration after Pilocarpine-Induced Status Epilepticus
title_short Downregulation of the Astroglial Connexin Expression and Neurodegeneration after Pilocarpine-Induced Status Epilepticus
title_sort downregulation of the astroglial connexin expression and neurodegeneration after pilocarpine-induced status epilepticus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9819917/
https://www.ncbi.nlm.nih.gov/pubmed/36613467
http://dx.doi.org/10.3390/ijms24010023
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