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Neuroligin-1 knockdown reduces survival of adult-generated newborn hippocampal neurons
Survival of adult-born hippocampal granule cells is modulated by neural activity, and thought to be enhanced by excitatory synaptic signaling. Here, we report that a reduction in the synaptogenic protein neuroligin-1 in adult-born neurons in vivo decreased their survival, but surprisingly, this effe...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3989658/ https://www.ncbi.nlm.nih.gov/pubmed/24782702 http://dx.doi.org/10.3389/fnins.2014.00071 |
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author | Schnell, Eric Long, Thomas H. Bensen, AeSoon L. Washburn, Eric K. Westbrook, Gary L. |
author_facet | Schnell, Eric Long, Thomas H. Bensen, AeSoon L. Washburn, Eric K. Westbrook, Gary L. |
author_sort | Schnell, Eric |
collection | PubMed |
description | Survival of adult-born hippocampal granule cells is modulated by neural activity, and thought to be enhanced by excitatory synaptic signaling. Here, we report that a reduction in the synaptogenic protein neuroligin-1 in adult-born neurons in vivo decreased their survival, but surprisingly, this effect was independent of changes in excitatory synaptic function. Instead, the decreased survival was associated with unexpected changes in dendrite and spine morphology during granule cell maturation, suggesting a link between cell growth and survival. |
format | Online Article Text |
id | pubmed-3989658 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-39896582014-04-29 Neuroligin-1 knockdown reduces survival of adult-generated newborn hippocampal neurons Schnell, Eric Long, Thomas H. Bensen, AeSoon L. Washburn, Eric K. Westbrook, Gary L. Front Neurosci Neuroscience Survival of adult-born hippocampal granule cells is modulated by neural activity, and thought to be enhanced by excitatory synaptic signaling. Here, we report that a reduction in the synaptogenic protein neuroligin-1 in adult-born neurons in vivo decreased their survival, but surprisingly, this effect was independent of changes in excitatory synaptic function. Instead, the decreased survival was associated with unexpected changes in dendrite and spine morphology during granule cell maturation, suggesting a link between cell growth and survival. Frontiers Media S.A. 2014-04-10 /pmc/articles/PMC3989658/ /pubmed/24782702 http://dx.doi.org/10.3389/fnins.2014.00071 Text en Copyright © 2014 Schnell, Long, Bensen, Washburn and Westbrook. 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 Schnell, Eric Long, Thomas H. Bensen, AeSoon L. Washburn, Eric K. Westbrook, Gary L. Neuroligin-1 knockdown reduces survival of adult-generated newborn hippocampal neurons |
title | Neuroligin-1 knockdown reduces survival of adult-generated newborn hippocampal neurons |
title_full | Neuroligin-1 knockdown reduces survival of adult-generated newborn hippocampal neurons |
title_fullStr | Neuroligin-1 knockdown reduces survival of adult-generated newborn hippocampal neurons |
title_full_unstemmed | Neuroligin-1 knockdown reduces survival of adult-generated newborn hippocampal neurons |
title_short | Neuroligin-1 knockdown reduces survival of adult-generated newborn hippocampal neurons |
title_sort | neuroligin-1 knockdown reduces survival of adult-generated newborn hippocampal neurons |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3989658/ https://www.ncbi.nlm.nih.gov/pubmed/24782702 http://dx.doi.org/10.3389/fnins.2014.00071 |
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