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When Are New Hippocampal Neurons, Born in the Adult Brain, Integrated into the Network That Processes Spatial Information?

Adult-born neurons in the dentate gyrus (DG) functionally integrate into the behaviorally relevant hippocampal networks, showing a specific Arc-expression response to spatial exploration when mature. However, it is not clear when, during the 4- to 6-week interval that is critical for survival and ma...

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Autores principales: Sandoval, C. Jimena, Martínez-Claros, Marisela, Bello-Medina, Paola C., Pérez, Oswaldo, Ramírez-Amaya, Víctor
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3052368/
https://www.ncbi.nlm.nih.gov/pubmed/21408012
http://dx.doi.org/10.1371/journal.pone.0017689
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author Sandoval, C. Jimena
Martínez-Claros, Marisela
Bello-Medina, Paola C.
Pérez, Oswaldo
Ramírez-Amaya, Víctor
author_facet Sandoval, C. Jimena
Martínez-Claros, Marisela
Bello-Medina, Paola C.
Pérez, Oswaldo
Ramírez-Amaya, Víctor
author_sort Sandoval, C. Jimena
collection PubMed
description Adult-born neurons in the dentate gyrus (DG) functionally integrate into the behaviorally relevant hippocampal networks, showing a specific Arc-expression response to spatial exploration when mature. However, it is not clear when, during the 4- to 6-week interval that is critical for survival and maturation of these neurons, this specific response develops. Therefore, we characterized Arc expression after spatial exploration or cage control conditions in adult-born neurons from rats that were injected with BrdU on one day and were sacrificed 1, 7, 15, 30, and 45 days post-BrdU injection (PBI). Triple immunostaining for NeuN, Arc, and BrdU was analyzed through the different DG layers. Arc protein expression in BrdU-positive cells was observed from day 1 to day 15 PBI but was not related to behavioral stimulation. The specific Arc-expression response to spatial exploration was observed from day 30 and 45 in about 5% of the BrdU-positive cell population. Most of the BrdU-positive neurons expressing Arc in response to spatial exploration (∼90%) were located in DG layer 1, and no Arc expression was observed in cells located in the subgranular zone (SGZ). Using the current data and that obtained previously, we propose a mathematical model suggesting that new neurons are unlikely to respond to exploration by expressing Arc after they are 301 days old, and also that in a 7-month-old rat the majority (60%) of the neurons that respond to exploration must have been born during adulthood; thus, suggesting that adult neurogenesis in the DG is highly relevant for spatial information processing.
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spelling pubmed-30523682011-03-15 When Are New Hippocampal Neurons, Born in the Adult Brain, Integrated into the Network That Processes Spatial Information? Sandoval, C. Jimena Martínez-Claros, Marisela Bello-Medina, Paola C. Pérez, Oswaldo Ramírez-Amaya, Víctor PLoS One Research Article Adult-born neurons in the dentate gyrus (DG) functionally integrate into the behaviorally relevant hippocampal networks, showing a specific Arc-expression response to spatial exploration when mature. However, it is not clear when, during the 4- to 6-week interval that is critical for survival and maturation of these neurons, this specific response develops. Therefore, we characterized Arc expression after spatial exploration or cage control conditions in adult-born neurons from rats that were injected with BrdU on one day and were sacrificed 1, 7, 15, 30, and 45 days post-BrdU injection (PBI). Triple immunostaining for NeuN, Arc, and BrdU was analyzed through the different DG layers. Arc protein expression in BrdU-positive cells was observed from day 1 to day 15 PBI but was not related to behavioral stimulation. The specific Arc-expression response to spatial exploration was observed from day 30 and 45 in about 5% of the BrdU-positive cell population. Most of the BrdU-positive neurons expressing Arc in response to spatial exploration (∼90%) were located in DG layer 1, and no Arc expression was observed in cells located in the subgranular zone (SGZ). Using the current data and that obtained previously, we propose a mathematical model suggesting that new neurons are unlikely to respond to exploration by expressing Arc after they are 301 days old, and also that in a 7-month-old rat the majority (60%) of the neurons that respond to exploration must have been born during adulthood; thus, suggesting that adult neurogenesis in the DG is highly relevant for spatial information processing. Public Library of Science 2011-03-09 /pmc/articles/PMC3052368/ /pubmed/21408012 http://dx.doi.org/10.1371/journal.pone.0017689 Text en Sandoval 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
Sandoval, C. Jimena
Martínez-Claros, Marisela
Bello-Medina, Paola C.
Pérez, Oswaldo
Ramírez-Amaya, Víctor
When Are New Hippocampal Neurons, Born in the Adult Brain, Integrated into the Network That Processes Spatial Information?
title When Are New Hippocampal Neurons, Born in the Adult Brain, Integrated into the Network That Processes Spatial Information?
title_full When Are New Hippocampal Neurons, Born in the Adult Brain, Integrated into the Network That Processes Spatial Information?
title_fullStr When Are New Hippocampal Neurons, Born in the Adult Brain, Integrated into the Network That Processes Spatial Information?
title_full_unstemmed When Are New Hippocampal Neurons, Born in the Adult Brain, Integrated into the Network That Processes Spatial Information?
title_short When Are New Hippocampal Neurons, Born in the Adult Brain, Integrated into the Network That Processes Spatial Information?
title_sort when are new hippocampal neurons, born in the adult brain, integrated into the network that processes spatial information?
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3052368/
https://www.ncbi.nlm.nih.gov/pubmed/21408012
http://dx.doi.org/10.1371/journal.pone.0017689
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