New Insights for GABA Function in the Central Nervous System

A special issue of Cells (ISSN 2073-4409). This special issue belongs to the section "Cells of the Nervous System".

Deadline for manuscript submissions: closed (29 February 2024) | Viewed by 1016

Special Issue Editors


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Guest Editor
Dominick P. Purpura Department of Neuroscience, Albert Einstein College of Medicine, Bronx, NY 10461, USA
Interests: synaptic function and plasticity; hippocampal neuro-circuits; epilepsy; cellular mechanisms of memory; neuropsychiatric diseases

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Guest Editor
INSERM, Aix Marseille University, UNIS, UMR1072, Marseille, France
Interests: axon physiology; STDP; plasticity of neuronal excitability; ion channels; inhibition
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Special Issue Information

Dear Colleagues,

A major challenge in neuroscience is to understand the cellular and molecular mechanisms underlying brain function and diseases. The brain is one of the most complex organs composed of different cell types. Inhibitory and excitatory neurons form intricate circuits underlying complex behaviors. Importantly, a well-balanced neuronal excitation and inhibition is crucial for proper brain function, while alterations in this balance are associated with a number of neurological and neuropsychiatric disorders, such as epilepsy and schizophrenia. This Special Issue will focus on γ-aminobutyric acid (GABA), the major inhibitory neurotransmitter in the central nervous system. GABA is very powerful in controlling neuronal excitability and information processing; however, several knowledge gaps remain regarding the role of GABAergic neurons, the regulation of GABA release and GABA receptors, GABA neuro- and glio-transmission, and synaptic plasticity.

This Special Issue aims to highlight new findings regarding the role GABA in the nervous system. A better understanding of GABA function may not only provide new insights into brain health, but it is also crucial for the development of more effective therapeutic approaches for several neuropathological conditions, involving dysregulations in the GABA system.

Dr. Kaoutsar Nasrallah
Prof. Dr. Dominique Debanne
Guest Editors

Manuscript Submission Information

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Published Papers (1 paper)

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Research

22 pages, 4044 KiB  
Article
Downregulation of Ribosomal Protein Genes Is Revealed in a Model of Rat Hippocampal Neuronal Culture Activation with GABA(A)R/GlyRa2 Antagonist Picrotoxin
by Alexander Beletskiy, Anastasia Zolotar, Polina Fortygina, Ekaterina Chesnokova, Leonid Uroshlev, Pavel Balaban and Peter Kolosov
Cells 2024, 13(5), 383; https://0-doi-org.brum.beds.ac.uk/10.3390/cells13050383 - 23 Feb 2024
Viewed by 697
Abstract
Long-read transcriptome sequencing provides us with a convenient tool for the thorough study of biological processes such as neuronal plasticity. Here, we aimed to perform transcriptional profiling of rat hippocampal primary neuron cultures after stimulation with picrotoxin (PTX) to further understand molecular mechanisms [...] Read more.
Long-read transcriptome sequencing provides us with a convenient tool for the thorough study of biological processes such as neuronal plasticity. Here, we aimed to perform transcriptional profiling of rat hippocampal primary neuron cultures after stimulation with picrotoxin (PTX) to further understand molecular mechanisms of neuronal activation. To overcome the limitations of short-read RNA-Seq approaches, we performed an Oxford Nanopore Technologies MinION-based long-read sequencing and transcriptome assembly of rat primary hippocampal culture mRNA at three time points after the PTX activation. We used a specific approach to exclude uncapped mRNAs during sample preparation. Overall, we found 23,652 novel transcripts in comparison to reference annotations, out of which ~6000 were entirely novel and mostly transposon-derived loci. Analysis of differentially expressed genes (DEG) showed that 3046 genes were differentially expressed, of which 2037 were upregulated and 1009 were downregulated at 30 min after the PTX application, with only 446 and 13 genes differentially expressed at 1 h and 5 h time points, respectively. Most notably, multiple genes encoding ribosomal proteins, with a high basal expression level, were downregulated after 30 min incubation with PTX; we suggest that this indicates redistribution of transcriptional resources towards activity-induced genes. Novel loci and isoforms observed in this study may help us further understand the functional mRNA repertoire in neuronal plasticity processes. Together with other NGS techniques, differential gene expression analysis of sequencing data obtained using MinION platform might provide a simple method to optimize further study of neuronal plasticity. Full article
(This article belongs to the Special Issue New Insights for GABA Function in the Central Nervous System)
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