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In vivo evaluation of cellular activity in αCaMKII heterozygous knockout mice using manganese-enhanced magnetic resonance imaging (MEMRI)

The alpha-calcium/calmodulin-dependent protein kinase II (αCaMKII) is a serine/threonine protein kinase predominantly expressed in the forebrain, especially in the postsynaptic density, and plays a key role in synaptic plasticity, learning and memory. αCaMKII heterozygous knockout (HKO) mice exhibit...

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Autores principales: Hattori, Satoko, Hagihara, Hideo, Ohira, Koji, Aoki, Ichio, Saga, Tsuneo, Suhara, Tetsuya, Higuchi, Makoto, Miyakawa, Tsuyoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3822296/
https://www.ncbi.nlm.nih.gov/pubmed/24273499
http://dx.doi.org/10.3389/fnint.2013.00076
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author Hattori, Satoko
Hagihara, Hideo
Ohira, Koji
Aoki, Ichio
Saga, Tsuneo
Suhara, Tetsuya
Higuchi, Makoto
Miyakawa, Tsuyoshi
author_facet Hattori, Satoko
Hagihara, Hideo
Ohira, Koji
Aoki, Ichio
Saga, Tsuneo
Suhara, Tetsuya
Higuchi, Makoto
Miyakawa, Tsuyoshi
author_sort Hattori, Satoko
collection PubMed
description The alpha-calcium/calmodulin-dependent protein kinase II (αCaMKII) is a serine/threonine protein kinase predominantly expressed in the forebrain, especially in the postsynaptic density, and plays a key role in synaptic plasticity, learning and memory. αCaMKII heterozygous knockout (HKO) mice exhibit abnormal emotional and aggressive behaviors and cognitive impairments and have been proposed as an animal model of psychiatric illness. Our previous studies have shown that the expression of immediate early genes (IEGs) after exposure to electric foot shock or after performing a working memory task is decreased in the hippocampus, central amygdala, and medial prefrontal cortex of mutant mice. These changes could be caused by disturbances in neuronal signal transduction; however, it is still unclear whether neuronal activity is reduced in these regions. In this study, we performed in vivo manganese-enhanced magnetic resonance imaging (MEMRI) to assess the regional cellular activity in the brains of αCaMKII HKO mice. The signal intensity of MEMRI 24 h after systemic MnCl(2) administration reflects functional increases of Mn(2+) influx into neurons and glia via transport mechanisms, such as voltage-gated and/or ligand-gated Ca(2+) channels. αCaMKII HKO mice demonstrated a low signal intensity of MEMRI in the dentate gyrus (DG), in which almost all neurons were at immature status at the molecular, morphological, and electrophysiological levels. In contrast, analysis of the signal intensity in these mutant mice revealed increased activity in the CA1 area of the hippocampus, a region crucial for cognitive function. The signal intensity was also increased in the bed nucleus of the stria terminalis (BNST), which is involved in anxiety. These changes in the mutant mice may be responsible for the observed dysregulated behaviors, such as cognitive deficit and abnormal anxiety-like behavior, which are similar to symptoms seen in human psychiatric disorders.
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spelling pubmed-38222962013-11-22 In vivo evaluation of cellular activity in αCaMKII heterozygous knockout mice using manganese-enhanced magnetic resonance imaging (MEMRI) Hattori, Satoko Hagihara, Hideo Ohira, Koji Aoki, Ichio Saga, Tsuneo Suhara, Tetsuya Higuchi, Makoto Miyakawa, Tsuyoshi Front Integr Neurosci Neuroscience The alpha-calcium/calmodulin-dependent protein kinase II (αCaMKII) is a serine/threonine protein kinase predominantly expressed in the forebrain, especially in the postsynaptic density, and plays a key role in synaptic plasticity, learning and memory. αCaMKII heterozygous knockout (HKO) mice exhibit abnormal emotional and aggressive behaviors and cognitive impairments and have been proposed as an animal model of psychiatric illness. Our previous studies have shown that the expression of immediate early genes (IEGs) after exposure to electric foot shock or after performing a working memory task is decreased in the hippocampus, central amygdala, and medial prefrontal cortex of mutant mice. These changes could be caused by disturbances in neuronal signal transduction; however, it is still unclear whether neuronal activity is reduced in these regions. In this study, we performed in vivo manganese-enhanced magnetic resonance imaging (MEMRI) to assess the regional cellular activity in the brains of αCaMKII HKO mice. The signal intensity of MEMRI 24 h after systemic MnCl(2) administration reflects functional increases of Mn(2+) influx into neurons and glia via transport mechanisms, such as voltage-gated and/or ligand-gated Ca(2+) channels. αCaMKII HKO mice demonstrated a low signal intensity of MEMRI in the dentate gyrus (DG), in which almost all neurons were at immature status at the molecular, morphological, and electrophysiological levels. In contrast, analysis of the signal intensity in these mutant mice revealed increased activity in the CA1 area of the hippocampus, a region crucial for cognitive function. The signal intensity was also increased in the bed nucleus of the stria terminalis (BNST), which is involved in anxiety. These changes in the mutant mice may be responsible for the observed dysregulated behaviors, such as cognitive deficit and abnormal anxiety-like behavior, which are similar to symptoms seen in human psychiatric disorders. Frontiers Media S.A. 2013-11-11 /pmc/articles/PMC3822296/ /pubmed/24273499 http://dx.doi.org/10.3389/fnint.2013.00076 Text en Copyright © 2013 Hattori, Hagihara, Ohira, Aoki, Saga, Suhara, Higuchi and Miyakawa. http://creativecommons.org/licenses/by/3.0/ 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) or licensor 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
Hattori, Satoko
Hagihara, Hideo
Ohira, Koji
Aoki, Ichio
Saga, Tsuneo
Suhara, Tetsuya
Higuchi, Makoto
Miyakawa, Tsuyoshi
In vivo evaluation of cellular activity in αCaMKII heterozygous knockout mice using manganese-enhanced magnetic resonance imaging (MEMRI)
title In vivo evaluation of cellular activity in αCaMKII heterozygous knockout mice using manganese-enhanced magnetic resonance imaging (MEMRI)
title_full In vivo evaluation of cellular activity in αCaMKII heterozygous knockout mice using manganese-enhanced magnetic resonance imaging (MEMRI)
title_fullStr In vivo evaluation of cellular activity in αCaMKII heterozygous knockout mice using manganese-enhanced magnetic resonance imaging (MEMRI)
title_full_unstemmed In vivo evaluation of cellular activity in αCaMKII heterozygous knockout mice using manganese-enhanced magnetic resonance imaging (MEMRI)
title_short In vivo evaluation of cellular activity in αCaMKII heterozygous knockout mice using manganese-enhanced magnetic resonance imaging (MEMRI)
title_sort in vivo evaluation of cellular activity in αcamkii heterozygous knockout mice using manganese-enhanced magnetic resonance imaging (memri)
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3822296/
https://www.ncbi.nlm.nih.gov/pubmed/24273499
http://dx.doi.org/10.3389/fnint.2013.00076
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