Deletion of hippocampal Glucocorticoid receptors unveils sex-biased microRNA expression and neuronal morphology alterations in mice

Sex differences in the brain have prompted many researchers to investigate the underlying molecular actors, such as the glucocorticoid receptor (GR). This nuclear receptor controls gene expression, including microRNAs (miRNAs), in non-neuronal cells. Here, we investigated sex-biased effects of GR on...

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Main Authors: Macarena Tejos-Bravo, Robert H. Oakley, Shannon D. Whirledge, Wladimir A. Corrales, Juan P. Silva, Gonzalo García-Rojo, Jorge Toledo, Wendy Sanchez, Luciano Román-Albasini, Esteban Aliaga, Felipe Aguayo, Felipe Olave, Vinicius Maracaja-Coutinho, John A. Cidlowski, Jenny L. Fiedler
Format: Article
Language:English
Published: Elsevier 2021-05-01
Series:Neurobiology of Stress
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S235228952100014X
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author Macarena Tejos-Bravo
Robert H. Oakley
Shannon D. Whirledge
Wladimir A. Corrales
Juan P. Silva
Gonzalo García-Rojo
Jorge Toledo
Wendy Sanchez
Luciano Román-Albasini
Esteban Aliaga
Felipe Aguayo
Felipe Olave
Vinicius Maracaja-Coutinho
John A. Cidlowski
Jenny L. Fiedler
spellingShingle Macarena Tejos-Bravo
Robert H. Oakley
Shannon D. Whirledge
Wladimir A. Corrales
Juan P. Silva
Gonzalo García-Rojo
Jorge Toledo
Wendy Sanchez
Luciano Román-Albasini
Esteban Aliaga
Felipe Aguayo
Felipe Olave
Vinicius Maracaja-Coutinho
John A. Cidlowski
Jenny L. Fiedler
Deletion of hippocampal Glucocorticoid receptors unveils sex-biased microRNA expression and neuronal morphology alterations in mice
Neurobiology of Stress
Glucocorticoid receptor
Hippocampus
miRNAs
Neuroplasticity
Dendrites
Dendritic spines
author_facet Macarena Tejos-Bravo
Robert H. Oakley
Shannon D. Whirledge
Wladimir A. Corrales
Juan P. Silva
Gonzalo García-Rojo
Jorge Toledo
Wendy Sanchez
Luciano Román-Albasini
Esteban Aliaga
Felipe Aguayo
Felipe Olave
Vinicius Maracaja-Coutinho
John A. Cidlowski
Jenny L. Fiedler
author_sort Macarena Tejos-Bravo
title Deletion of hippocampal Glucocorticoid receptors unveils sex-biased microRNA expression and neuronal morphology alterations in mice
title_short Deletion of hippocampal Glucocorticoid receptors unveils sex-biased microRNA expression and neuronal morphology alterations in mice
title_full Deletion of hippocampal Glucocorticoid receptors unveils sex-biased microRNA expression and neuronal morphology alterations in mice
title_fullStr Deletion of hippocampal Glucocorticoid receptors unveils sex-biased microRNA expression and neuronal morphology alterations in mice
title_full_unstemmed Deletion of hippocampal Glucocorticoid receptors unveils sex-biased microRNA expression and neuronal morphology alterations in mice
title_sort deletion of hippocampal glucocorticoid receptors unveils sex-biased microrna expression and neuronal morphology alterations in mice
publisher Elsevier
series Neurobiology of Stress
issn 2352-2895
publishDate 2021-05-01
description Sex differences in the brain have prompted many researchers to investigate the underlying molecular actors, such as the glucocorticoid receptor (GR). This nuclear receptor controls gene expression, including microRNAs (miRNAs), in non-neuronal cells. Here, we investigated sex-biased effects of GR on hippocampal miRNA expression and neuronal morphology by generating a neuron-specific GR knockout mouse (Emx1-Nr3c1−/−). The levels of 578 mature miRNAs were assessed using NanoString technology and, in contrast to males, female Emx1-Nr3c1−/− mice showed a substantially higher number of differentially expressed miRNAs, confirming a sex-biased effect of GR ablation. Based on bioinformatic analyses we identified several transcription factors potentially involved in miRNA regulation. Functional enrichment analyses of the miRNA-mRNA interactions revealed pathways related to neuronal arborization and both spine morphology and density in both sexes. Two recognized regulators of dendritic morphology, CAMKII-α and GSK-3β, increased their protein levels by GR ablation in female mice hippocampus, without changes in males. Additionally, sex-specific effects of GR deletion were observed on CA1 neuronal arborization and dendritic spine features. For instance, a reduced density of mushroom spines in apical dendrites was evidenced only in females, while a decreased length in basal dendrites was noted only in males. However, length and arborization of apical dendrites were reduced by GR ablation irrespective of the sex. Overall, our study provides new insights into the sex-biased GR actions, especially in terms of miRNAs expression and neuronal morphology in the hippocampus.
topic Glucocorticoid receptor
Hippocampus
miRNAs
Neuroplasticity
Dendrites
Dendritic spines
url http://www.sciencedirect.com/science/article/pii/S235228952100014X
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spelling doaj-551a49ab2e4540a89888e326634030772021-05-16T04:23:41ZengElsevierNeurobiology of Stress2352-28952021-05-0114100306Deletion of hippocampal Glucocorticoid receptors unveils sex-biased microRNA expression and neuronal morphology alterations in miceMacarena Tejos-Bravo0Robert H. Oakley1Shannon D. Whirledge2Wladimir A. Corrales3Juan P. Silva4Gonzalo García-Rojo5Jorge Toledo6Wendy Sanchez7Luciano Román-Albasini8Esteban Aliaga9Felipe Aguayo10Felipe Olave11Vinicius Maracaja-Coutinho12John A. Cidlowski13Jenny L. Fiedler14Laboratory of Neuroplasticity and Neurogenetics, Faculty of Chemical and Pharmaceutical Sciences, Department of Biochemistry and Molecular Biology, Universidad de Chile, Independencia, 8380492, Santiago, ChileSignal Transduction Laboratory, National Institute of Environmental Health Sciences, National Institutes of Health, Department of Health and Human Services, Research Triangle Park, NC, 27709, USASignal Transduction Laboratory, National Institute of Environmental Health Sciences, National Institutes of Health, Department of Health and Human Services, Research Triangle Park, NC, 27709, USALaboratory of Neuroplasticity and Neurogenetics, Faculty of Chemical and Pharmaceutical Sciences, Department of Biochemistry and Molecular Biology, Universidad de Chile, Independencia, 8380492, Santiago, ChileLaboratory of Neuroplasticity and Neurogenetics, Faculty of Chemical and Pharmaceutical Sciences, Department of Biochemistry and Molecular Biology, Universidad de Chile, Independencia, 8380492, Santiago, ChileLaboratory of Neuroplasticity and Neurogenetics, Faculty of Chemical and Pharmaceutical Sciences, Department of Biochemistry and Molecular Biology, Universidad de Chile, Independencia, 8380492, Santiago, Chile; Carrera de Odontología. Facultad de Ciencias, Universidad de La Serena, La Serena, ChileLaboratory of Scientific Image Analysis (SCIAN-Lab), Biomedical Neuroscience Institute, Faculty of Medicine, Universidad de Chile, Independencia 1027, Santiago, 8380453, ChileLaboratory of Scientific Image Analysis (SCIAN-Lab), Biomedical Neuroscience Institute, Faculty of Medicine, Universidad de Chile, Independencia 1027, Santiago, 8380453, ChileLaboratory of Neuroplasticity and Neurogenetics, Faculty of Chemical and Pharmaceutical Sciences, Department of Biochemistry and Molecular Biology, Universidad de Chile, Independencia, 8380492, Santiago, ChileDepartment of Kinesiology and the Neuropsychology and Cognitive Neurosciences Research Center (CINPSI-Neurocog), Faculty of Health Sciences, Universidad Católica del Maule, Talca, ChileLaboratory of Neuroplasticity and Neurogenetics, Faculty of Chemical and Pharmaceutical Sciences, Department of Biochemistry and Molecular Biology, Universidad de Chile, Independencia, 8380492, Santiago, ChileLaboratory of Neuroplasticity and Neurogenetics, Faculty of Chemical and Pharmaceutical Sciences, Department of Biochemistry and Molecular Biology, Universidad de Chile, Independencia, 8380492, Santiago, ChileAdvanced Center for Chronic Diseases -ACCDiS. Faculty of Chemical and Pharmaceutical Sciences. Department of Biochemistry and Molecular Biology. Universidad de Chile, Independencia, 8380492, Santiago, Chile; Corresponding author. Department of Biochemistry and Molecular Biology, Faculty of Chemical and Pharmaceutical Sciences, Universidad de Chile, Santiago, Chile.Signal Transduction Laboratory, National Institute of Environmental Health Sciences, National Institutes of Health, Department of Health and Human Services, Research Triangle Park, NC, 27709, USA; Corresponding author. Signal Transduction Laboratory, NIEHS, NIH, DHHS, 111 T.W. Alexander Drive, Research Triangle Park, NC, 27709, USA.Laboratory of Neuroplasticity and Neurogenetics, Faculty of Chemical and Pharmaceutical Sciences, Department of Biochemistry and Molecular Biology, Universidad de Chile, Independencia, 8380492, Santiago, Chile; Corresponding author. Department of Biochemistry and Molecular Biology, Faculty of Chemical and Pharmaceutical Sciences, Universidad de Chile, Santiago, Chile.Sex differences in the brain have prompted many researchers to investigate the underlying molecular actors, such as the glucocorticoid receptor (GR). This nuclear receptor controls gene expression, including microRNAs (miRNAs), in non-neuronal cells. Here, we investigated sex-biased effects of GR on hippocampal miRNA expression and neuronal morphology by generating a neuron-specific GR knockout mouse (Emx1-Nr3c1−/−). The levels of 578 mature miRNAs were assessed using NanoString technology and, in contrast to males, female Emx1-Nr3c1−/− mice showed a substantially higher number of differentially expressed miRNAs, confirming a sex-biased effect of GR ablation. Based on bioinformatic analyses we identified several transcription factors potentially involved in miRNA regulation. Functional enrichment analyses of the miRNA-mRNA interactions revealed pathways related to neuronal arborization and both spine morphology and density in both sexes. Two recognized regulators of dendritic morphology, CAMKII-α and GSK-3β, increased their protein levels by GR ablation in female mice hippocampus, without changes in males. Additionally, sex-specific effects of GR deletion were observed on CA1 neuronal arborization and dendritic spine features. For instance, a reduced density of mushroom spines in apical dendrites was evidenced only in females, while a decreased length in basal dendrites was noted only in males. However, length and arborization of apical dendrites were reduced by GR ablation irrespective of the sex. Overall, our study provides new insights into the sex-biased GR actions, especially in terms of miRNAs expression and neuronal morphology in the hippocampus.http://www.sciencedirect.com/science/article/pii/S235228952100014XGlucocorticoid receptorHippocampusmiRNAsNeuroplasticityDendritesDendritic spines