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Boosting adult neurogenesis to enhance sensory performance
Although most mammalian neurons are born prenatally, there are at least a couple of specialised niches in the adult rodent brain that continually generate new neurons throughout life. The potential functions conferred by this process of adult neurogenesis, however, remain obscure, despite a sizeable...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6418449/ https://www.ncbi.nlm.nih.gov/pubmed/30787183 http://dx.doi.org/10.15252/embj.2019101589 |
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author | Lipovsek, Marcela Grubb, Matthew S |
author_facet | Lipovsek, Marcela Grubb, Matthew S |
author_sort | Lipovsek, Marcela |
collection | PubMed |
description | Although most mammalian neurons are born prenatally, there are at least a couple of specialised niches in the adult rodent brain that continually generate new neurons throughout life. The potential functions conferred by this process of adult neurogenesis, however, remain obscure, despite a sizeable literature exploring the links between alterations in neurogenic capacity and changes in behavioural ability. A new study by Bragado Alonso et al (2019) offers a novel viewpoint on this question by describing a particularly clean way to manipulate adult neurogenesis. Specifically altering cell cycle dynamics in adult neural stem cells leads to an increase in new‐born neuron production without altering those extra cells’ morphological or functional properties. Moreover, mice with boosted adult neurogenesis are significantly better at discriminating highly similar sensory stimuli. |
format | Online Article Text |
id | pubmed-6418449 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-64184492019-03-27 Boosting adult neurogenesis to enhance sensory performance Lipovsek, Marcela Grubb, Matthew S EMBO J News & Views Although most mammalian neurons are born prenatally, there are at least a couple of specialised niches in the adult rodent brain that continually generate new neurons throughout life. The potential functions conferred by this process of adult neurogenesis, however, remain obscure, despite a sizeable literature exploring the links between alterations in neurogenic capacity and changes in behavioural ability. A new study by Bragado Alonso et al (2019) offers a novel viewpoint on this question by describing a particularly clean way to manipulate adult neurogenesis. Specifically altering cell cycle dynamics in adult neural stem cells leads to an increase in new‐born neuron production without altering those extra cells’ morphological or functional properties. Moreover, mice with boosted adult neurogenesis are significantly better at discriminating highly similar sensory stimuli. John Wiley and Sons Inc. 2019-02-20 2019-03-15 /pmc/articles/PMC6418449/ /pubmed/30787183 http://dx.doi.org/10.15252/embj.2019101589 Text en © 2019 The Authors. Published under the terms of the CC BY 4.0 license This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | News & Views Lipovsek, Marcela Grubb, Matthew S Boosting adult neurogenesis to enhance sensory performance |
title | Boosting adult neurogenesis to enhance sensory performance |
title_full | Boosting adult neurogenesis to enhance sensory performance |
title_fullStr | Boosting adult neurogenesis to enhance sensory performance |
title_full_unstemmed | Boosting adult neurogenesis to enhance sensory performance |
title_short | Boosting adult neurogenesis to enhance sensory performance |
title_sort | boosting adult neurogenesis to enhance sensory performance |
topic | News & Views |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6418449/ https://www.ncbi.nlm.nih.gov/pubmed/30787183 http://dx.doi.org/10.15252/embj.2019101589 |
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