Cargando…

Immature morphological properties in subcellular-scale structures in the dentate gyrus of Schnurri-2 knockout mice: a model for schizophrenia and intellectual disability

Accumulating evidence suggests that subcellular-scale structures such as dendritic spine and mitochondria may be involved in the pathogenesis/pathophysiology of schizophrenia and intellectual disability. Previously, we proposed mice lacking Schnurri-2 (Shn2; also called major histocompatibility comp...

Descripción completa

Detalles Bibliográficos
Autores principales: Nakao, Akito, Miyazaki, Naoyuki, Ohira, Koji, Hagihara, Hideo, Takagi, Tsuyoshi, Usuda, Nobuteru, Ishii, Shunsuke, Murata, Kazuyoshi, Miyakawa, Tsuyoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5727961/
https://www.ncbi.nlm.nih.gov/pubmed/29233179
http://dx.doi.org/10.1186/s13041-017-0339-2
_version_ 1783285984772751360
author Nakao, Akito
Miyazaki, Naoyuki
Ohira, Koji
Hagihara, Hideo
Takagi, Tsuyoshi
Usuda, Nobuteru
Ishii, Shunsuke
Murata, Kazuyoshi
Miyakawa, Tsuyoshi
author_facet Nakao, Akito
Miyazaki, Naoyuki
Ohira, Koji
Hagihara, Hideo
Takagi, Tsuyoshi
Usuda, Nobuteru
Ishii, Shunsuke
Murata, Kazuyoshi
Miyakawa, Tsuyoshi
author_sort Nakao, Akito
collection PubMed
description Accumulating evidence suggests that subcellular-scale structures such as dendritic spine and mitochondria may be involved in the pathogenesis/pathophysiology of schizophrenia and intellectual disability. Previously, we proposed mice lacking Schnurri-2 (Shn2; also called major histocompatibility complex [MHC]-binding protein 2 [MBP-2], or human immunodeficiency virus type I enhancer binding protein 2 [HIVEP2]) as a schizophrenia and intellectual disability model with mild chronic inflammation. In the mutants’ brains, there are increases in C4b and C1q genes, which are considered to mediate synapse elimination during postnatal development. However, morphological properties of subcellular-scale structures such as dendritic spine in Shn2 knockout (KO) mice remain unknown. In this study, we conducted three-dimensional morphological analyses in subcellular-scale structures in dentate gyrus granule cells of Shn2 KO mice by serial block-face scanning electron microscopy. Shn2 KO mice showed immature dendritic spine morphology characterized by increases in spine length and decreases in spine diameter. There was a non-significant tendency toward decrease in spine density of Shn2 KO mice over wild-type mice, and spine volume was indistinguishable between genotypes. Shn2 KO mice exhibited a significant reduction in GluR1 expression and a nominally significant decrease in SV2 expression, while PSD95 expression had a non-significant tendency to decrease in Shn2 KO mice. There were significant decreases in dendrite diameter, nuclear volume, and the number of constricted mitochondria in the mutants. Additionally, neuronal density was elevated in Shn2 KO mice. These results suggest that Shn2 KO mice serve as a unique tool for investigating morphological abnormalities of subcellular-scale structures in schizophrenia, intellectual disability, and its related disorders. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13041-017-0339-2) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-5727961
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-57279612017-12-18 Immature morphological properties in subcellular-scale structures in the dentate gyrus of Schnurri-2 knockout mice: a model for schizophrenia and intellectual disability Nakao, Akito Miyazaki, Naoyuki Ohira, Koji Hagihara, Hideo Takagi, Tsuyoshi Usuda, Nobuteru Ishii, Shunsuke Murata, Kazuyoshi Miyakawa, Tsuyoshi Mol Brain Research Accumulating evidence suggests that subcellular-scale structures such as dendritic spine and mitochondria may be involved in the pathogenesis/pathophysiology of schizophrenia and intellectual disability. Previously, we proposed mice lacking Schnurri-2 (Shn2; also called major histocompatibility complex [MHC]-binding protein 2 [MBP-2], or human immunodeficiency virus type I enhancer binding protein 2 [HIVEP2]) as a schizophrenia and intellectual disability model with mild chronic inflammation. In the mutants’ brains, there are increases in C4b and C1q genes, which are considered to mediate synapse elimination during postnatal development. However, morphological properties of subcellular-scale structures such as dendritic spine in Shn2 knockout (KO) mice remain unknown. In this study, we conducted three-dimensional morphological analyses in subcellular-scale structures in dentate gyrus granule cells of Shn2 KO mice by serial block-face scanning electron microscopy. Shn2 KO mice showed immature dendritic spine morphology characterized by increases in spine length and decreases in spine diameter. There was a non-significant tendency toward decrease in spine density of Shn2 KO mice over wild-type mice, and spine volume was indistinguishable between genotypes. Shn2 KO mice exhibited a significant reduction in GluR1 expression and a nominally significant decrease in SV2 expression, while PSD95 expression had a non-significant tendency to decrease in Shn2 KO mice. There were significant decreases in dendrite diameter, nuclear volume, and the number of constricted mitochondria in the mutants. Additionally, neuronal density was elevated in Shn2 KO mice. These results suggest that Shn2 KO mice serve as a unique tool for investigating morphological abnormalities of subcellular-scale structures in schizophrenia, intellectual disability, and its related disorders. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13041-017-0339-2) contains supplementary material, which is available to authorized users. BioMed Central 2017-12-12 /pmc/articles/PMC5727961/ /pubmed/29233179 http://dx.doi.org/10.1186/s13041-017-0339-2 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Nakao, Akito
Miyazaki, Naoyuki
Ohira, Koji
Hagihara, Hideo
Takagi, Tsuyoshi
Usuda, Nobuteru
Ishii, Shunsuke
Murata, Kazuyoshi
Miyakawa, Tsuyoshi
Immature morphological properties in subcellular-scale structures in the dentate gyrus of Schnurri-2 knockout mice: a model for schizophrenia and intellectual disability
title Immature morphological properties in subcellular-scale structures in the dentate gyrus of Schnurri-2 knockout mice: a model for schizophrenia and intellectual disability
title_full Immature morphological properties in subcellular-scale structures in the dentate gyrus of Schnurri-2 knockout mice: a model for schizophrenia and intellectual disability
title_fullStr Immature morphological properties in subcellular-scale structures in the dentate gyrus of Schnurri-2 knockout mice: a model for schizophrenia and intellectual disability
title_full_unstemmed Immature morphological properties in subcellular-scale structures in the dentate gyrus of Schnurri-2 knockout mice: a model for schizophrenia and intellectual disability
title_short Immature morphological properties in subcellular-scale structures in the dentate gyrus of Schnurri-2 knockout mice: a model for schizophrenia and intellectual disability
title_sort immature morphological properties in subcellular-scale structures in the dentate gyrus of schnurri-2 knockout mice: a model for schizophrenia and intellectual disability
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5727961/
https://www.ncbi.nlm.nih.gov/pubmed/29233179
http://dx.doi.org/10.1186/s13041-017-0339-2
work_keys_str_mv AT nakaoakito immaturemorphologicalpropertiesinsubcellularscalestructuresinthedentategyrusofschnurri2knockoutmiceamodelforschizophreniaandintellectualdisability
AT miyazakinaoyuki immaturemorphologicalpropertiesinsubcellularscalestructuresinthedentategyrusofschnurri2knockoutmiceamodelforschizophreniaandintellectualdisability
AT ohirakoji immaturemorphologicalpropertiesinsubcellularscalestructuresinthedentategyrusofschnurri2knockoutmiceamodelforschizophreniaandintellectualdisability
AT hagiharahideo immaturemorphologicalpropertiesinsubcellularscalestructuresinthedentategyrusofschnurri2knockoutmiceamodelforschizophreniaandintellectualdisability
AT takagitsuyoshi immaturemorphologicalpropertiesinsubcellularscalestructuresinthedentategyrusofschnurri2knockoutmiceamodelforschizophreniaandintellectualdisability
AT usudanobuteru immaturemorphologicalpropertiesinsubcellularscalestructuresinthedentategyrusofschnurri2knockoutmiceamodelforschizophreniaandintellectualdisability
AT ishiishunsuke immaturemorphologicalpropertiesinsubcellularscalestructuresinthedentategyrusofschnurri2knockoutmiceamodelforschizophreniaandintellectualdisability
AT muratakazuyoshi immaturemorphologicalpropertiesinsubcellularscalestructuresinthedentategyrusofschnurri2knockoutmiceamodelforschizophreniaandintellectualdisability
AT miyakawatsuyoshi immaturemorphologicalpropertiesinsubcellularscalestructuresinthedentategyrusofschnurri2knockoutmiceamodelforschizophreniaandintellectualdisability