Foxg1 Upregulation Enhances Neocortical Activity.


Journal

Cerebral cortex (New York, N.Y. : 1991)
ISSN: 1460-2199
Titre abrégé: Cereb Cortex
Pays: United States
ID NLM: 9110718

Informations de publication

Date de publication:
30 07 2020
Historique:
received: 20 02 2020
revised: 03 04 2020
accepted: 05 04 2020
pubmed: 10 5 2020
medline: 15 12 2021
entrez: 9 5 2020
Statut: ppublish

Résumé

Foxg1 is an ancient transcription factor gene orchestrating a number of neurodevelopmental processes taking place in the rostral brain. In this study, we investigated its impact on neocortical activity. We found that mice overexpressing Foxg1 in neocortical pyramidal cells displayed an electroencephalography (EEG) with increased spike frequency and were more prone to kainic acid (KA)-induced seizures. Consistently, primary cultures of neocortical neurons gain-of-function for Foxg1 were hyperactive and hypersynchronized. That reflected an unbalanced expression of key genes encoding for ion channels, gamma aminobutyric acid and glutamate receptors, and was likely exacerbated by a pronounced interneuron depletion. We also detected a transient Foxg1 upregulation ignited in turn by neuronal activity and mediated by immediate early genes. Based on this, we propose that even small changes of Foxg1 levels may result in a profound impact on pyramidal cell activity, an issue relevant to neuronal physiology and neurological aberrancies associated to FOXG1 copy number variations.

Identifiants

pubmed: 32383447
pii: 5831513
doi: 10.1093/cercor/bhaa107
doi:

Substances chimiques

Forkhead Transcription Factors 0
Foxg1 protein, mouse 0
Nerve Tissue Proteins 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

5147-5165

Informations de copyright

© The Author(s) 2020. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permission@oup.com.

Auteurs

Wendalina Tigani (W)

Laboratory of Cerebral Cortex Development, Neuroscience Area, SISSA, Trieste 34136, Italy.

Moira Pinzan Rossi (MP)

Laboratory of Cerebral Cortex Development, Neuroscience Area, SISSA, Trieste 34136, Italy.
AgenTus Therapeutics, Inc., Cambridge CB4 OWG, United Kingdom.

Osvaldo Artimagnella (O)

Laboratory of Cerebral Cortex Development, Neuroscience Area, SISSA, Trieste 34136, Italy.

Manuela Santo (M)

Laboratory of Cerebral Cortex Development, Neuroscience Area, SISSA, Trieste 34136, Italy.

Rossana Rauti (R)

Laboratory of Neurons and Nanomaterials, Neuroscience Area, SISSA, Trieste 34136, Italy.
Dept. Biomedical Engineering, Tel Aviv University, Tel Aviv 6997801, Israel.

Teresa Sorbo (T)

Laboratory of Neurons and Nanomaterials, Neuroscience Area, SISSA, Trieste 34136, Italy.

Francesco Paolo Ulloa Severino (FP)

Laboratory of Bionanotechnologies, Neuroscience Area, SISSA, Trieste 34136, Italy.
Cell Biology Dept, Duke University Medical Center, Duke University, Durham NC-27710, USA.

Giovanni Provenzano (G)

Department of Cellular, Computational, and Integrative Biology (CIBIO), University of Trento, Trento 38123, Italy.

Manuela Allegra (M)

Neuroscience Institute, Neurophysiology Section, National Research Council (CNR), Pisa 56124, Italy.
Laboratory G5 Circuits Neuronaux, Institut Pasteur, Paris 75015, France.

Matteo Caleo (M)

Neuroscience Institute, Neurophysiology Section, National Research Council (CNR), Pisa 56124, Italy.
Department of Biomedical Sciences, University of Padua, Padua 35121, Italy.

Laura Ballerini (L)

Laboratory of Neurons and Nanomaterials, Neuroscience Area, SISSA, Trieste 34136, Italy.

Yuri Bozzi (Y)

Neuroscience Institute, Neurophysiology Section, National Research Council (CNR), Pisa 56124, Italy.
Center for Mind/Brain Sciences, University of Trento, Trento 38068, Italy.

Antonello Mallamaci (A)

Laboratory of Cerebral Cortex Development, Neuroscience Area, SISSA, Trieste 34136, Italy.

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