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Early Dendritic Morphogenesis of Adult-Born Dentate Granule Cells Is Regulated by FHL2

Dentate granule cells (DGCs), the progeny of neural stem cells (NSCs) in the sub-granular zone of the dentate gyrus (DG), must develop and functionally integrate with the mature cohort of neurons in order to maintain critical hippocampal functions throughout adulthood. Dysregulation in the continuum...

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Autores principales: Ahamad, Afrinash, Wang, Jia, Ge, Shaoyu, Kirschen, Gregory W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7090230/
https://www.ncbi.nlm.nih.gov/pubmed/32256309
http://dx.doi.org/10.3389/fnins.2020.00202
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author Ahamad, Afrinash
Wang, Jia
Ge, Shaoyu
Kirschen, Gregory W.
author_facet Ahamad, Afrinash
Wang, Jia
Ge, Shaoyu
Kirschen, Gregory W.
author_sort Ahamad, Afrinash
collection PubMed
description Dentate granule cells (DGCs), the progeny of neural stem cells (NSCs) in the sub-granular zone of the dentate gyrus (DG), must develop and functionally integrate with the mature cohort of neurons in order to maintain critical hippocampal functions throughout adulthood. Dysregulation in the continuum of DGC development can result in aberrant morphology and disrupted functional maturation, impairing neuroplasticity of the network. Yet, the molecular underpinnings of the signaling involved in adult-born DGC maturation including dendritic growth, which correlates with functional integration, remains incompletely understood. Given the high metabolic activity in the dentate gyrus (DG) required to achieve continuous neurogenesis, we investigated the potential regulatory role of a cellular metabolism-linked gene recently implicated in NSC cycling and neuroblast migration, called Four and a half LIM domain 2 (FHL2). The FHL2 protein modulates numerous pathways related to proliferation, migration, survival and cytoskeletal rearrangement in peripheral tissues, interacting with the machinery of the sphingosine-1-phosphate pathway, also known to be highly active especially in the hippocampus. Yet, the potential relevance of FHL2 to adult-born DGC development remains unknown. To elucidate the role of FHL2 in DGC development in the adult brain, we first confirmed the endogenous expression of FHL2 in NSCs and new granule cells within the DG, then engineered viral vectors for genetic manipulation experiments, investigating morphological changes in early stages of DGC development. Overexpression of FHL2 during early DGC development resulted in marked sprouting and branching of dendrites, while silencing of FHL2 increased dendritic length. Together, these findings suggest a novel role of FHL2 in adult-born DGC morphological maturation, which may open up a new line of investigation regarding the relevance of this gene in physiology and pathologies of the hippocampus such as mesial temporal lobe epilepsy (MTLE).
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spelling pubmed-70902302020-03-31 Early Dendritic Morphogenesis of Adult-Born Dentate Granule Cells Is Regulated by FHL2 Ahamad, Afrinash Wang, Jia Ge, Shaoyu Kirschen, Gregory W. Front Neurosci Neuroscience Dentate granule cells (DGCs), the progeny of neural stem cells (NSCs) in the sub-granular zone of the dentate gyrus (DG), must develop and functionally integrate with the mature cohort of neurons in order to maintain critical hippocampal functions throughout adulthood. Dysregulation in the continuum of DGC development can result in aberrant morphology and disrupted functional maturation, impairing neuroplasticity of the network. Yet, the molecular underpinnings of the signaling involved in adult-born DGC maturation including dendritic growth, which correlates with functional integration, remains incompletely understood. Given the high metabolic activity in the dentate gyrus (DG) required to achieve continuous neurogenesis, we investigated the potential regulatory role of a cellular metabolism-linked gene recently implicated in NSC cycling and neuroblast migration, called Four and a half LIM domain 2 (FHL2). The FHL2 protein modulates numerous pathways related to proliferation, migration, survival and cytoskeletal rearrangement in peripheral tissues, interacting with the machinery of the sphingosine-1-phosphate pathway, also known to be highly active especially in the hippocampus. Yet, the potential relevance of FHL2 to adult-born DGC development remains unknown. To elucidate the role of FHL2 in DGC development in the adult brain, we first confirmed the endogenous expression of FHL2 in NSCs and new granule cells within the DG, then engineered viral vectors for genetic manipulation experiments, investigating morphological changes in early stages of DGC development. Overexpression of FHL2 during early DGC development resulted in marked sprouting and branching of dendrites, while silencing of FHL2 increased dendritic length. Together, these findings suggest a novel role of FHL2 in adult-born DGC morphological maturation, which may open up a new line of investigation regarding the relevance of this gene in physiology and pathologies of the hippocampus such as mesial temporal lobe epilepsy (MTLE). Frontiers Media S.A. 2020-03-17 /pmc/articles/PMC7090230/ /pubmed/32256309 http://dx.doi.org/10.3389/fnins.2020.00202 Text en Copyright © 2020 Ahamad, Wang, Ge and Kirschen. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Ahamad, Afrinash
Wang, Jia
Ge, Shaoyu
Kirschen, Gregory W.
Early Dendritic Morphogenesis of Adult-Born Dentate Granule Cells Is Regulated by FHL2
title Early Dendritic Morphogenesis of Adult-Born Dentate Granule Cells Is Regulated by FHL2
title_full Early Dendritic Morphogenesis of Adult-Born Dentate Granule Cells Is Regulated by FHL2
title_fullStr Early Dendritic Morphogenesis of Adult-Born Dentate Granule Cells Is Regulated by FHL2
title_full_unstemmed Early Dendritic Morphogenesis of Adult-Born Dentate Granule Cells Is Regulated by FHL2
title_short Early Dendritic Morphogenesis of Adult-Born Dentate Granule Cells Is Regulated by FHL2
title_sort early dendritic morphogenesis of adult-born dentate granule cells is regulated by fhl2
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7090230/
https://www.ncbi.nlm.nih.gov/pubmed/32256309
http://dx.doi.org/10.3389/fnins.2020.00202
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