Adult-born neurons modify excitatory synaptic transmission to existing neurons

Adult-born neurons are continually produced in the dentate gyrus but it is unclear whether synaptic integration of new neurons affects the pre-existing circuit. Here we investigated how manipulating neurogenesis in adult mice alters excitatory synaptic transmission to mature dentate neurons. Enhanci...

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Main Authors: Elena W Adlaf, Ryan J Vaden, Anastasia J Niver, Allison F Manuel, Vincent C Onyilo, Matheus T Araujo, Cristina V Dieni, Hai T Vo, Gwendalyn D King, Jacques I Wadiche, Linda Overstreet-Wadiche
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2017-01-01
Series:eLife
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Online Access:https://elifesciences.org/articles/19886
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author Elena W Adlaf
Ryan J Vaden
Anastasia J Niver
Allison F Manuel
Vincent C Onyilo
Matheus T Araujo
Cristina V Dieni
Hai T Vo
Gwendalyn D King
Jacques I Wadiche
Linda Overstreet-Wadiche
author_facet Elena W Adlaf
Ryan J Vaden
Anastasia J Niver
Allison F Manuel
Vincent C Onyilo
Matheus T Araujo
Cristina V Dieni
Hai T Vo
Gwendalyn D King
Jacques I Wadiche
Linda Overstreet-Wadiche
author_sort Elena W Adlaf
collection DOAJ
description Adult-born neurons are continually produced in the dentate gyrus but it is unclear whether synaptic integration of new neurons affects the pre-existing circuit. Here we investigated how manipulating neurogenesis in adult mice alters excitatory synaptic transmission to mature dentate neurons. Enhancing neurogenesis by conditional deletion of the pro-apoptotic gene Bax in stem cells reduced excitatory postsynaptic currents (EPSCs) and spine density in mature neurons, whereas genetic ablation of neurogenesis increased EPSCs in mature neurons. Unexpectedly, we found that Bax deletion in developing and mature dentate neurons increased EPSCs and prevented neurogenesis-induced synaptic suppression. Together these results show that neurogenesis modifies synaptic transmission to mature neurons in a manner consistent with a redistribution of pre-existing synapses to newly integrating neurons and that a non-apoptotic function of the Bax signaling pathway contributes to ongoing synaptic refinement within the dentate circuit.
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spelling doaj.art-1742315f915a44d686adaa1ef0fa6d672022-12-22T03:24:56ZengeLife Sciences Publications LtdeLife2050-084X2017-01-01610.7554/eLife.19886Adult-born neurons modify excitatory synaptic transmission to existing neuronsElena W Adlaf0Ryan J Vaden1Anastasia J Niver2Allison F Manuel3Vincent C Onyilo4Matheus T Araujo5Cristina V Dieni6Hai T Vo7Gwendalyn D King8https://orcid.org/0000-0002-3659-9241Jacques I Wadiche9https://orcid.org/0000-0001-8180-2061Linda Overstreet-Wadiche10https://orcid.org/0000-0001-7367-5998Department of Neurobiology, University of Alabama at Birmingham, Birmingham, United StatesDepartment of Neurobiology, University of Alabama at Birmingham, Birmingham, United StatesDepartment of Neurobiology, University of Alabama at Birmingham, Birmingham, United StatesDepartment of Neurobiology, University of Alabama at Birmingham, Birmingham, United StatesDepartment of Neurobiology, University of Alabama at Birmingham, Birmingham, United StatesDepartment of Neurobiology, University of Alabama at Birmingham, Birmingham, United StatesDepartment of Neurobiology, University of Alabama at Birmingham, Birmingham, United StatesDepartment of Neurobiology, University of Alabama at Birmingham, Birmingham, United StatesDepartment of Neurobiology, University of Alabama at Birmingham, Birmingham, United StatesDepartment of Neurobiology, University of Alabama at Birmingham, Birmingham, United StatesDepartment of Neurobiology, University of Alabama at Birmingham, Birmingham, United StatesAdult-born neurons are continually produced in the dentate gyrus but it is unclear whether synaptic integration of new neurons affects the pre-existing circuit. Here we investigated how manipulating neurogenesis in adult mice alters excitatory synaptic transmission to mature dentate neurons. Enhancing neurogenesis by conditional deletion of the pro-apoptotic gene Bax in stem cells reduced excitatory postsynaptic currents (EPSCs) and spine density in mature neurons, whereas genetic ablation of neurogenesis increased EPSCs in mature neurons. Unexpectedly, we found that Bax deletion in developing and mature dentate neurons increased EPSCs and prevented neurogenesis-induced synaptic suppression. Together these results show that neurogenesis modifies synaptic transmission to mature neurons in a manner consistent with a redistribution of pre-existing synapses to newly integrating neurons and that a non-apoptotic function of the Bax signaling pathway contributes to ongoing synaptic refinement within the dentate circuit.https://elifesciences.org/articles/19886adult neurogenesisdentate gyrussynaptic transmissionEPSCcompetitiongranule cells
spellingShingle Elena W Adlaf
Ryan J Vaden
Anastasia J Niver
Allison F Manuel
Vincent C Onyilo
Matheus T Araujo
Cristina V Dieni
Hai T Vo
Gwendalyn D King
Jacques I Wadiche
Linda Overstreet-Wadiche
Adult-born neurons modify excitatory synaptic transmission to existing neurons
eLife
adult neurogenesis
dentate gyrus
synaptic transmission
EPSC
competition
granule cells
title Adult-born neurons modify excitatory synaptic transmission to existing neurons
title_full Adult-born neurons modify excitatory synaptic transmission to existing neurons
title_fullStr Adult-born neurons modify excitatory synaptic transmission to existing neurons
title_full_unstemmed Adult-born neurons modify excitatory synaptic transmission to existing neurons
title_short Adult-born neurons modify excitatory synaptic transmission to existing neurons
title_sort adult born neurons modify excitatory synaptic transmission to existing neurons
topic adult neurogenesis
dentate gyrus
synaptic transmission
EPSC
competition
granule cells
url https://elifesciences.org/articles/19886
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