Dendritic spine density is increased on nucleus accumbens D2 neurons after chronic social defeat

Abstract Stress alters the structure and function of brain reward circuitry and is an important risk factor for developing depression. In the nucleus accumbens (NAc), structural and physiological plasticity of medium spiny neurons (MSNs) have been linked to increased stress-related and depression-li...

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Main Authors: Megan E. Fox, Antonio Figueiredo, Miriam S. Menken, Mary Kay Lobo
Format: Article
Language:English
Published: Nature Publishing Group 2020-07-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-020-69339-7
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spelling doaj-d16bc7fad6024b85a3b46d766c46053b2021-07-25T11:20:18ZengNature Publishing GroupScientific Reports2045-23222020-07-011011710.1038/s41598-020-69339-7Dendritic spine density is increased on nucleus accumbens D2 neurons after chronic social defeatMegan E. Fox0Antonio Figueiredo1Miriam S. Menken2Mary Kay Lobo3Department of Anatomy and Neurobiology, University of Maryland School of MedicineDepartment of Anatomy and Neurobiology, University of Maryland School of MedicineDepartment of Anatomy and Neurobiology, University of Maryland School of MedicineDepartment of Anatomy and Neurobiology, University of Maryland School of MedicineAbstract Stress alters the structure and function of brain reward circuitry and is an important risk factor for developing depression. In the nucleus accumbens (NAc), structural and physiological plasticity of medium spiny neurons (MSNs) have been linked to increased stress-related and depression-like behaviors. NAc MSNs have opposing roles in driving stress-related behaviors that is dependent on their dopamine receptor expression. After chronic social defeat stress, NAc MSNs exhibit increased dendritic spine density. However, it remains unclear if the dendritic spine plasticity is MSN subtype specific. Here we use viral labeling to characterize dendritic spine morphology specifically in dopamine D2 receptor expressing MSNs (D2-MSNs). After chronic social defeat, D2-MSNs exhibit increased spine density that is correlated with enhanced social avoidance behavior. Together, our data indicate dendritic spine plasticity is MSN subtype specific, improving our understanding of structural plasticity after chronic stress.https://doi.org/10.1038/s41598-020-69339-7
collection DOAJ
language English
format Article
sources DOAJ
author Megan E. Fox
Antonio Figueiredo
Miriam S. Menken
Mary Kay Lobo
spellingShingle Megan E. Fox
Antonio Figueiredo
Miriam S. Menken
Mary Kay Lobo
Dendritic spine density is increased on nucleus accumbens D2 neurons after chronic social defeat
Scientific Reports
author_facet Megan E. Fox
Antonio Figueiredo
Miriam S. Menken
Mary Kay Lobo
author_sort Megan E. Fox
title Dendritic spine density is increased on nucleus accumbens D2 neurons after chronic social defeat
title_short Dendritic spine density is increased on nucleus accumbens D2 neurons after chronic social defeat
title_full Dendritic spine density is increased on nucleus accumbens D2 neurons after chronic social defeat
title_fullStr Dendritic spine density is increased on nucleus accumbens D2 neurons after chronic social defeat
title_full_unstemmed Dendritic spine density is increased on nucleus accumbens D2 neurons after chronic social defeat
title_sort dendritic spine density is increased on nucleus accumbens d2 neurons after chronic social defeat
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2020-07-01
description Abstract Stress alters the structure and function of brain reward circuitry and is an important risk factor for developing depression. In the nucleus accumbens (NAc), structural and physiological plasticity of medium spiny neurons (MSNs) have been linked to increased stress-related and depression-like behaviors. NAc MSNs have opposing roles in driving stress-related behaviors that is dependent on their dopamine receptor expression. After chronic social defeat stress, NAc MSNs exhibit increased dendritic spine density. However, it remains unclear if the dendritic spine plasticity is MSN subtype specific. Here we use viral labeling to characterize dendritic spine morphology specifically in dopamine D2 receptor expressing MSNs (D2-MSNs). After chronic social defeat, D2-MSNs exhibit increased spine density that is correlated with enhanced social avoidance behavior. Together, our data indicate dendritic spine plasticity is MSN subtype specific, improving our understanding of structural plasticity after chronic stress.
url https://doi.org/10.1038/s41598-020-69339-7
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