Cargando…
Transgenic miR132 Alters Neuronal Spine Density and Impairs Novel Object Recognition Memory
Inducible gene expression plays a central role in neuronal plasticity, learning, and memory, and dysfunction of the underlying molecular events can lead to severe neuronal disorders. In addition to coding transcripts (mRNAs), non-coding microRNAs (miRNAs) appear to play a role in these processes. Fo...
Autores principales: | , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2993964/ https://www.ncbi.nlm.nih.gov/pubmed/21124738 http://dx.doi.org/10.1371/journal.pone.0015497 |
_version_ | 1782192869229985792 |
---|---|
author | Hansen, Katelin F. Sakamoto, Kensuke Wayman, Gary A. Impey, Soren Obrietan, Karl |
author_facet | Hansen, Katelin F. Sakamoto, Kensuke Wayman, Gary A. Impey, Soren Obrietan, Karl |
author_sort | Hansen, Katelin F. |
collection | PubMed |
description | Inducible gene expression plays a central role in neuronal plasticity, learning, and memory, and dysfunction of the underlying molecular events can lead to severe neuronal disorders. In addition to coding transcripts (mRNAs), non-coding microRNAs (miRNAs) appear to play a role in these processes. For instance, the CREB-regulated miRNA miR132 has been shown to affect neuronal structure in an activity-dependent manner, yet the details of its physiological effects and the behavioral consequences in vivo remain unclear. To examine these questions, we employed a transgenic mouse strain that expresses miR132 in forebrain neurons. Morphometric analysis of hippocampal neurons revealed that transgenic miR132 triggers a marked increase in dendritic spine density. Additionally, miR132 transgenic mice exhibited a decrease in the expression of MeCP2, a protein implicated in Rett Syndrome and other disorders of mental retardation. Consistent with these findings, miR132 transgenic mice displayed significant deficits in novel object recognition. Together, these data support a role for miR132 as a regulator of neuronal structure and function, and raise the possibility that dysregulation of miR132 could contribute to an array of cognitive disorders. |
format | Text |
id | pubmed-2993964 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-29939642010-12-01 Transgenic miR132 Alters Neuronal Spine Density and Impairs Novel Object Recognition Memory Hansen, Katelin F. Sakamoto, Kensuke Wayman, Gary A. Impey, Soren Obrietan, Karl PLoS One Research Article Inducible gene expression plays a central role in neuronal plasticity, learning, and memory, and dysfunction of the underlying molecular events can lead to severe neuronal disorders. In addition to coding transcripts (mRNAs), non-coding microRNAs (miRNAs) appear to play a role in these processes. For instance, the CREB-regulated miRNA miR132 has been shown to affect neuronal structure in an activity-dependent manner, yet the details of its physiological effects and the behavioral consequences in vivo remain unclear. To examine these questions, we employed a transgenic mouse strain that expresses miR132 in forebrain neurons. Morphometric analysis of hippocampal neurons revealed that transgenic miR132 triggers a marked increase in dendritic spine density. Additionally, miR132 transgenic mice exhibited a decrease in the expression of MeCP2, a protein implicated in Rett Syndrome and other disorders of mental retardation. Consistent with these findings, miR132 transgenic mice displayed significant deficits in novel object recognition. Together, these data support a role for miR132 as a regulator of neuronal structure and function, and raise the possibility that dysregulation of miR132 could contribute to an array of cognitive disorders. Public Library of Science 2010-11-29 /pmc/articles/PMC2993964/ /pubmed/21124738 http://dx.doi.org/10.1371/journal.pone.0015497 Text en Hansen 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 Hansen, Katelin F. Sakamoto, Kensuke Wayman, Gary A. Impey, Soren Obrietan, Karl Transgenic miR132 Alters Neuronal Spine Density and Impairs Novel Object Recognition Memory |
title | Transgenic miR132 Alters Neuronal Spine Density and Impairs Novel Object Recognition Memory |
title_full | Transgenic miR132 Alters Neuronal Spine Density and Impairs Novel Object Recognition Memory |
title_fullStr | Transgenic miR132 Alters Neuronal Spine Density and Impairs Novel Object Recognition Memory |
title_full_unstemmed | Transgenic miR132 Alters Neuronal Spine Density and Impairs Novel Object Recognition Memory |
title_short | Transgenic miR132 Alters Neuronal Spine Density and Impairs Novel Object Recognition Memory |
title_sort | transgenic mir132 alters neuronal spine density and impairs novel object recognition memory |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2993964/ https://www.ncbi.nlm.nih.gov/pubmed/21124738 http://dx.doi.org/10.1371/journal.pone.0015497 |
work_keys_str_mv | AT hansenkatelinf transgenicmir132altersneuronalspinedensityandimpairsnovelobjectrecognitionmemory AT sakamotokensuke transgenicmir132altersneuronalspinedensityandimpairsnovelobjectrecognitionmemory AT waymangarya transgenicmir132altersneuronalspinedensityandimpairsnovelobjectrecognitionmemory AT impeysoren transgenicmir132altersneuronalspinedensityandimpairsnovelobjectrecognitionmemory AT obrietankarl transgenicmir132altersneuronalspinedensityandimpairsnovelobjectrecognitionmemory |