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Ultrastructural analyses in the hippocampus CA1 field in Shank3-deficient mice

BACKGROUND: The genetics of autism spectrum disorder (hereafter referred to as “autism”) are rapidly unfolding, with a significant increase in the identification of genes implicated in the disorder. Many of these genes are part of a complex landscape of genetic variants that are thought to act toget...

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Autores principales: Uppal, Neha, Puri, Rishi, Yuk, Frank, Janssen, William G M, Bozdagi-Gunal, Ozlem, Harony-Nicolas, Hala, Dickstein, Dara L, Buxbaum, Joseph D, Hof, Patrick R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4486760/
https://www.ncbi.nlm.nih.gov/pubmed/26137200
http://dx.doi.org/10.1186/s13229-015-0036-x
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author Uppal, Neha
Puri, Rishi
Yuk, Frank
Janssen, William G M
Bozdagi-Gunal, Ozlem
Harony-Nicolas, Hala
Dickstein, Dara L
Buxbaum, Joseph D
Hof, Patrick R
author_facet Uppal, Neha
Puri, Rishi
Yuk, Frank
Janssen, William G M
Bozdagi-Gunal, Ozlem
Harony-Nicolas, Hala
Dickstein, Dara L
Buxbaum, Joseph D
Hof, Patrick R
author_sort Uppal, Neha
collection PubMed
description BACKGROUND: The genetics of autism spectrum disorder (hereafter referred to as “autism”) are rapidly unfolding, with a significant increase in the identification of genes implicated in the disorder. Many of these genes are part of a complex landscape of genetic variants that are thought to act together to cause the behavioral phenotype associated with autism. One of the few single-locus causes of autism involves a mutation in the SH3 and multiple ankyrin repeat domains 3 (SHANK3) gene. Previous electrophysiological studies in mice with Shank3 mutations demonstrated impairment in synaptic long-term potentiation, suggesting a potential disruption at the synapse. METHODS: To understand how variants in SHANK3 would lead to such impairments and manifest in the brain of patients with autism, we assessed the presence of synaptic pathology in Shank3-deficient mice at 5 weeks and 3 months of age, focusing on the stratum radiatum of the CA1 field. This study analyzed both Shank3 heterozygous and homozygous mice using an electron microscopy approach to determine whether there is a morphological correlate to the synaptic functional impairment. RESULTS: As both synaptic strength and plasticity are affected in Shank3-deficient mice, we hypothesized that there would be a reduction in synapse density, postsynaptic density length, and perforated synapse density. No differences were found in most parameters assessed. However, Shank3 heterozygotes had significantly higher numbers of perforated synapses at 5 weeks compared to 3 months of age and significantly higher numbers of perforated synapses compared to 5-week-old wildtype and Shank3 homozygous mice. CONCLUSIONS: Although this finding represents preliminary evidence for ultrastructural alterations, it suggests that while major structural changes seem to be compensated for in Shank3-deficient mice, more subtle morphological alterations, affecting synaptic structure, may take place in an age-dependent manner.
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spelling pubmed-44867602015-07-02 Ultrastructural analyses in the hippocampus CA1 field in Shank3-deficient mice Uppal, Neha Puri, Rishi Yuk, Frank Janssen, William G M Bozdagi-Gunal, Ozlem Harony-Nicolas, Hala Dickstein, Dara L Buxbaum, Joseph D Hof, Patrick R Mol Autism Research BACKGROUND: The genetics of autism spectrum disorder (hereafter referred to as “autism”) are rapidly unfolding, with a significant increase in the identification of genes implicated in the disorder. Many of these genes are part of a complex landscape of genetic variants that are thought to act together to cause the behavioral phenotype associated with autism. One of the few single-locus causes of autism involves a mutation in the SH3 and multiple ankyrin repeat domains 3 (SHANK3) gene. Previous electrophysiological studies in mice with Shank3 mutations demonstrated impairment in synaptic long-term potentiation, suggesting a potential disruption at the synapse. METHODS: To understand how variants in SHANK3 would lead to such impairments and manifest in the brain of patients with autism, we assessed the presence of synaptic pathology in Shank3-deficient mice at 5 weeks and 3 months of age, focusing on the stratum radiatum of the CA1 field. This study analyzed both Shank3 heterozygous and homozygous mice using an electron microscopy approach to determine whether there is a morphological correlate to the synaptic functional impairment. RESULTS: As both synaptic strength and plasticity are affected in Shank3-deficient mice, we hypothesized that there would be a reduction in synapse density, postsynaptic density length, and perforated synapse density. No differences were found in most parameters assessed. However, Shank3 heterozygotes had significantly higher numbers of perforated synapses at 5 weeks compared to 3 months of age and significantly higher numbers of perforated synapses compared to 5-week-old wildtype and Shank3 homozygous mice. CONCLUSIONS: Although this finding represents preliminary evidence for ultrastructural alterations, it suggests that while major structural changes seem to be compensated for in Shank3-deficient mice, more subtle morphological alterations, affecting synaptic structure, may take place in an age-dependent manner. BioMed Central 2015-06-30 /pmc/articles/PMC4486760/ /pubmed/26137200 http://dx.doi.org/10.1186/s13229-015-0036-x Text en © Uppal et al. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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
Uppal, Neha
Puri, Rishi
Yuk, Frank
Janssen, William G M
Bozdagi-Gunal, Ozlem
Harony-Nicolas, Hala
Dickstein, Dara L
Buxbaum, Joseph D
Hof, Patrick R
Ultrastructural analyses in the hippocampus CA1 field in Shank3-deficient mice
title Ultrastructural analyses in the hippocampus CA1 field in Shank3-deficient mice
title_full Ultrastructural analyses in the hippocampus CA1 field in Shank3-deficient mice
title_fullStr Ultrastructural analyses in the hippocampus CA1 field in Shank3-deficient mice
title_full_unstemmed Ultrastructural analyses in the hippocampus CA1 field in Shank3-deficient mice
title_short Ultrastructural analyses in the hippocampus CA1 field in Shank3-deficient mice
title_sort ultrastructural analyses in the hippocampus ca1 field in shank3-deficient mice
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4486760/
https://www.ncbi.nlm.nih.gov/pubmed/26137200
http://dx.doi.org/10.1186/s13229-015-0036-x
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