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Sex-Dependent Novelty Response in Neurexin-1α Mutant Mice
Neurexin-1 alpha (NRXN1α) belongs to the family of cell adhesion molecules (CAMs), which are involved in the formation of neuronal networks and synapses. NRXN1α gene mutations have been identified in neuropsychiatric diseases including Schizophrenia (SCZ) and Autism Spectrum Disorder (ASD). In order...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3278455/ https://www.ncbi.nlm.nih.gov/pubmed/22348092 http://dx.doi.org/10.1371/journal.pone.0031503 |
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author | Laarakker, Marijke C. Reinders, Niels R. Bruining, Hilgo Ophoff, Roel A. Kas, Martien J. H. |
author_facet | Laarakker, Marijke C. Reinders, Niels R. Bruining, Hilgo Ophoff, Roel A. Kas, Martien J. H. |
author_sort | Laarakker, Marijke C. |
collection | PubMed |
description | Neurexin-1 alpha (NRXN1α) belongs to the family of cell adhesion molecules (CAMs), which are involved in the formation of neuronal networks and synapses. NRXN1α gene mutations have been identified in neuropsychiatric diseases including Schizophrenia (SCZ) and Autism Spectrum Disorder (ASD). In order to get a better understanding of the pleiotropic behavioral manifestations caused by NRXN1α gene mutations, we performed a behavioral study of Nrxn1α heterozygous knock-out (+/−) mice and observed increased responsiveness to novelty and accelerated habituation to novel environments compared to wild type (+/+) litter-mates. However, this effect was mainly observed in male mice, strongly suggesting that gender-specific mechanisms play an important role in Nrxn1α-induced phenotypes. |
format | Online Article Text |
id | pubmed-3278455 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-32784552012-02-17 Sex-Dependent Novelty Response in Neurexin-1α Mutant Mice Laarakker, Marijke C. Reinders, Niels R. Bruining, Hilgo Ophoff, Roel A. Kas, Martien J. H. PLoS One Research Article Neurexin-1 alpha (NRXN1α) belongs to the family of cell adhesion molecules (CAMs), which are involved in the formation of neuronal networks and synapses. NRXN1α gene mutations have been identified in neuropsychiatric diseases including Schizophrenia (SCZ) and Autism Spectrum Disorder (ASD). In order to get a better understanding of the pleiotropic behavioral manifestations caused by NRXN1α gene mutations, we performed a behavioral study of Nrxn1α heterozygous knock-out (+/−) mice and observed increased responsiveness to novelty and accelerated habituation to novel environments compared to wild type (+/+) litter-mates. However, this effect was mainly observed in male mice, strongly suggesting that gender-specific mechanisms play an important role in Nrxn1α-induced phenotypes. Public Library of Science 2012-02-13 /pmc/articles/PMC3278455/ /pubmed/22348092 http://dx.doi.org/10.1371/journal.pone.0031503 Text en Laarakker 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 Laarakker, Marijke C. Reinders, Niels R. Bruining, Hilgo Ophoff, Roel A. Kas, Martien J. H. Sex-Dependent Novelty Response in Neurexin-1α Mutant Mice |
title | Sex-Dependent Novelty Response in Neurexin-1α Mutant Mice |
title_full | Sex-Dependent Novelty Response in Neurexin-1α Mutant Mice |
title_fullStr | Sex-Dependent Novelty Response in Neurexin-1α Mutant Mice |
title_full_unstemmed | Sex-Dependent Novelty Response in Neurexin-1α Mutant Mice |
title_short | Sex-Dependent Novelty Response in Neurexin-1α Mutant Mice |
title_sort | sex-dependent novelty response in neurexin-1α mutant mice |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3278455/ https://www.ncbi.nlm.nih.gov/pubmed/22348092 http://dx.doi.org/10.1371/journal.pone.0031503 |
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