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Generation and Behavior Characterization of CaMKIIβ Knockout Mice
The calcium/calmodulin-dependent protein kinase II (CaMKII) is abundant in the brain, where it makes important contributions to synaptic organization and homeostasis, including playing an essential role in synaptic plasticity and memory. Four genes encode isoforms of CaMKII (α, β, δ, γ), with CaMKII...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4134274/ https://www.ncbi.nlm.nih.gov/pubmed/25127391 http://dx.doi.org/10.1371/journal.pone.0105191 |
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author | Bachstetter, Adam D. Webster, Scott J. Tu, Tao Goulding, Danielle S. Haiech, Jacques Watterson, D. Martin Van Eldik, Linda J. |
author_facet | Bachstetter, Adam D. Webster, Scott J. Tu, Tao Goulding, Danielle S. Haiech, Jacques Watterson, D. Martin Van Eldik, Linda J. |
author_sort | Bachstetter, Adam D. |
collection | PubMed |
description | The calcium/calmodulin-dependent protein kinase II (CaMKII) is abundant in the brain, where it makes important contributions to synaptic organization and homeostasis, including playing an essential role in synaptic plasticity and memory. Four genes encode isoforms of CaMKII (α, β, δ, γ), with CaMKIIα and CaMKIIβ highly expressed in the brain. Decades of molecular and cellular research, as well as the use of a large number of CaMKIIα mutant mouse lines, have provided insight into the pivotal roles of CaMKIIα in brain plasticity and cognition. However, less is known about the CaMKIIβ isoform. We report the development and extensive behavioral and phenotypic characterization of a CaMKIIβ knockout (KO) mouse. The CaMKIIβ KO mouse was found to be smaller at weaning, with an altered body mass composition. The CaMKIIβ KO mouse showed ataxia, impaired forelimb grip strength, and deficits in the rotorod, balance beam and running wheel tasks. Interestingly, the CaMKIIβ KO mouse exhibited reduced anxiety in the elevated plus maze and open field tests. The CaMKIIβ KO mouse also showed cognitive impairment in the novel object recognition task. Our results provide a comprehensive behavioral characterization of mice deficient in the β isoform of CaMKII. The neurologic phenotypes and the construction of the genotype suggest the utility of this KO mouse strain for future studies of CaMKIIβ in brain structure, function and development. |
format | Online Article Text |
id | pubmed-4134274 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-41342742014-08-19 Generation and Behavior Characterization of CaMKIIβ Knockout Mice Bachstetter, Adam D. Webster, Scott J. Tu, Tao Goulding, Danielle S. Haiech, Jacques Watterson, D. Martin Van Eldik, Linda J. PLoS One Research Article The calcium/calmodulin-dependent protein kinase II (CaMKII) is abundant in the brain, where it makes important contributions to synaptic organization and homeostasis, including playing an essential role in synaptic plasticity and memory. Four genes encode isoforms of CaMKII (α, β, δ, γ), with CaMKIIα and CaMKIIβ highly expressed in the brain. Decades of molecular and cellular research, as well as the use of a large number of CaMKIIα mutant mouse lines, have provided insight into the pivotal roles of CaMKIIα in brain plasticity and cognition. However, less is known about the CaMKIIβ isoform. We report the development and extensive behavioral and phenotypic characterization of a CaMKIIβ knockout (KO) mouse. The CaMKIIβ KO mouse was found to be smaller at weaning, with an altered body mass composition. The CaMKIIβ KO mouse showed ataxia, impaired forelimb grip strength, and deficits in the rotorod, balance beam and running wheel tasks. Interestingly, the CaMKIIβ KO mouse exhibited reduced anxiety in the elevated plus maze and open field tests. The CaMKIIβ KO mouse also showed cognitive impairment in the novel object recognition task. Our results provide a comprehensive behavioral characterization of mice deficient in the β isoform of CaMKII. The neurologic phenotypes and the construction of the genotype suggest the utility of this KO mouse strain for future studies of CaMKIIβ in brain structure, function and development. Public Library of Science 2014-08-15 /pmc/articles/PMC4134274/ /pubmed/25127391 http://dx.doi.org/10.1371/journal.pone.0105191 Text en © 2014 Bachstetter et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Bachstetter, Adam D. Webster, Scott J. Tu, Tao Goulding, Danielle S. Haiech, Jacques Watterson, D. Martin Van Eldik, Linda J. Generation and Behavior Characterization of CaMKIIβ Knockout Mice |
title | Generation and Behavior Characterization of CaMKIIβ Knockout Mice |
title_full | Generation and Behavior Characterization of CaMKIIβ Knockout Mice |
title_fullStr | Generation and Behavior Characterization of CaMKIIβ Knockout Mice |
title_full_unstemmed | Generation and Behavior Characterization of CaMKIIβ Knockout Mice |
title_short | Generation and Behavior Characterization of CaMKIIβ Knockout Mice |
title_sort | generation and behavior characterization of camkiiβ knockout mice |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4134274/ https://www.ncbi.nlm.nih.gov/pubmed/25127391 http://dx.doi.org/10.1371/journal.pone.0105191 |
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