Nr4a2 Transcription Factor in Hippocampal Synaptic Plasticity, Memory and Cognitive Dysfunction: A Perspective Review

Long-lasting changes of synaptic efficacy are largely mediated by activity-induced gene transcription and are essential for neuronal plasticity and memory. In this scenario, transcription factors have emerged as pivotal players underlying synaptic plasticity and the modification of neural networks r...

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Autores principales: Judit Català-Solsona, Alfredo J. Miñano-Molina, José Rodríguez-Álvarez
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Publicado: Frontiers Media S.A. 2021
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spelling oai:doaj.org-article:99a7cbcf432644129474a539475b73ca2021-11-22T05:19:06ZNr4a2 Transcription Factor in Hippocampal Synaptic Plasticity, Memory and Cognitive Dysfunction: A Perspective Review1662-509910.3389/fnmol.2021.786226https://doaj.org/article/99a7cbcf432644129474a539475b73ca2021-11-01T00:00:00Zhttps://www.frontiersin.org/articles/10.3389/fnmol.2021.786226/fullhttps://doaj.org/toc/1662-5099Long-lasting changes of synaptic efficacy are largely mediated by activity-induced gene transcription and are essential for neuronal plasticity and memory. In this scenario, transcription factors have emerged as pivotal players underlying synaptic plasticity and the modification of neural networks required for memory formation and consolidation. Hippocampal synaptic dysfunction is widely accepted to underlie the cognitive decline observed in some neurodegenerative disorders including Alzheimer’s disease. Therefore, understanding the molecular pathways regulating gene expression profiles may help to identify new synaptic therapeutic targets. The nuclear receptor 4A subfamily (Nr4a) of transcription factors has been involved in a variety of physiological processes within the hippocampus, ranging from inflammation to neuroprotection. Recent studies have also pointed out a role for the activity-dependent nuclear receptor subfamily 4, group A, member 2 (Nr4a2/Nurr1) in hippocampal synaptic plasticity and cognitive functions, although the underlying molecular mechanisms are still poorly understood. In this review, we highlight the specific effects of Nr4a2 in hippocampal synaptic plasticity and memory formation and we discuss whether the dysregulation of this transcription factor could contribute to hippocampal synaptic dysfunction, altogether suggesting the possibility that Nr4a2 may emerge as a novel synaptic therapeutic target in brain pathologies associated to cognitive dysfunctions.Judit Català-SolsonaJudit Català-SolsonaAlfredo J. Miñano-MolinaAlfredo J. Miñano-MolinaJosé Rodríguez-ÁlvarezJosé Rodríguez-ÁlvarezJosé Rodríguez-ÁlvarezFrontiers Media S.A.articleNr4a2transcription factorhippocampussynaptic plasticitybrainlearningNeurosciences. Biological psychiatry. NeuropsychiatryRC321-571ENFrontiers in Molecular Neuroscience, Vol 14 (2021)
institution DOAJ
collection DOAJ
language EN
topic Nr4a2
transcription factor
hippocampus
synaptic plasticity
brain
learning
Neurosciences. Biological psychiatry. Neuropsychiatry
RC321-571
spellingShingle Nr4a2
transcription factor
hippocampus
synaptic plasticity
brain
learning
Neurosciences. Biological psychiatry. Neuropsychiatry
RC321-571
Judit Català-Solsona
Judit Català-Solsona
Alfredo J. Miñano-Molina
Alfredo J. Miñano-Molina
José Rodríguez-Álvarez
José Rodríguez-Álvarez
José Rodríguez-Álvarez
Nr4a2 Transcription Factor in Hippocampal Synaptic Plasticity, Memory and Cognitive Dysfunction: A Perspective Review
description Long-lasting changes of synaptic efficacy are largely mediated by activity-induced gene transcription and are essential for neuronal plasticity and memory. In this scenario, transcription factors have emerged as pivotal players underlying synaptic plasticity and the modification of neural networks required for memory formation and consolidation. Hippocampal synaptic dysfunction is widely accepted to underlie the cognitive decline observed in some neurodegenerative disorders including Alzheimer’s disease. Therefore, understanding the molecular pathways regulating gene expression profiles may help to identify new synaptic therapeutic targets. The nuclear receptor 4A subfamily (Nr4a) of transcription factors has been involved in a variety of physiological processes within the hippocampus, ranging from inflammation to neuroprotection. Recent studies have also pointed out a role for the activity-dependent nuclear receptor subfamily 4, group A, member 2 (Nr4a2/Nurr1) in hippocampal synaptic plasticity and cognitive functions, although the underlying molecular mechanisms are still poorly understood. In this review, we highlight the specific effects of Nr4a2 in hippocampal synaptic plasticity and memory formation and we discuss whether the dysregulation of this transcription factor could contribute to hippocampal synaptic dysfunction, altogether suggesting the possibility that Nr4a2 may emerge as a novel synaptic therapeutic target in brain pathologies associated to cognitive dysfunctions.
format article
author Judit Català-Solsona
Judit Català-Solsona
Alfredo J. Miñano-Molina
Alfredo J. Miñano-Molina
José Rodríguez-Álvarez
José Rodríguez-Álvarez
José Rodríguez-Álvarez
author_facet Judit Català-Solsona
Judit Català-Solsona
Alfredo J. Miñano-Molina
Alfredo J. Miñano-Molina
José Rodríguez-Álvarez
José Rodríguez-Álvarez
José Rodríguez-Álvarez
author_sort Judit Català-Solsona
title Nr4a2 Transcription Factor in Hippocampal Synaptic Plasticity, Memory and Cognitive Dysfunction: A Perspective Review
title_short Nr4a2 Transcription Factor in Hippocampal Synaptic Plasticity, Memory and Cognitive Dysfunction: A Perspective Review
title_full Nr4a2 Transcription Factor in Hippocampal Synaptic Plasticity, Memory and Cognitive Dysfunction: A Perspective Review
title_fullStr Nr4a2 Transcription Factor in Hippocampal Synaptic Plasticity, Memory and Cognitive Dysfunction: A Perspective Review
title_full_unstemmed Nr4a2 Transcription Factor in Hippocampal Synaptic Plasticity, Memory and Cognitive Dysfunction: A Perspective Review
title_sort nr4a2 transcription factor in hippocampal synaptic plasticity, memory and cognitive dysfunction: a perspective review
publisher Frontiers Media S.A.
publishDate 2021
url https://doaj.org/article/99a7cbcf432644129474a539475b73ca
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