Morphological analysis of activity-reduced adult-born neurons in the mouse olfactory bulb

Adult born neurons are added to the olfactory bulb (OB) throughout life in rodents. While many factors have been identified as regulating the survival and integration of adult-born neurons (ABNs) into existing circuitry, the understanding of how these factors affect ABN morphology and connectivity...

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Main Authors: Jeffrey E Dahlen, Daniel A Jimenez, Richard C Gerkin, Nathan N Urban
Format: Article
Language:English
Published: Frontiers Media S.A. 2011-05-01
Series:Frontiers in Neuroscience
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fnins.2011.00066/full
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spelling doaj-048fc8ddf4bb4307a56ad65945773aca2020-11-24T21:11:08ZengFrontiers Media S.A.Frontiers in Neuroscience1662-453X2011-05-01510.3389/fnins.2011.000668904Morphological analysis of activity-reduced adult-born neurons in the mouse olfactory bulbJeffrey E Dahlen0Daniel A Jimenez1Daniel A Jimenez2Richard C Gerkin3Richard C Gerkin4Nathan N Urban5Nathan N Urban6Nathan N Urban7Carnegie Mellon UniversityUniversity of PittsburghCarnegie Mellon University & University of PittsburghCarnegie Mellon UniversityCarnegie Mellon University & University of PittsburghCarnegie Mellon UniversityUniversity of PittsburghCarnegie Mellon University & University of PittsburghAdult born neurons are added to the olfactory bulb (OB) throughout life in rodents. While many factors have been identified as regulating the survival and integration of adult-born neurons (ABNs) into existing circuitry, the understanding of how these factors affect ABN morphology and connectivity is limited. Here we compare how cell intrinsic (siRNA knock down of voltage gated sodium channels NaV1.1-1.3) and circuit level (naris occlusion) reductions in activity affect ABN morphology during integration into the OB. We found that both manipulations reduce the number of dendritic spines (and thus likely the number of reciprocal synaptic connections) formed with the surrounding circuitry and inhibited dendritic ramification of ABNs. Further, we identified regions of ABN apical dendrites where the largest and most significant decreases occur following siRNA knock down or naris occlusion. In siRNA knock down cells, reduction of spines is observed in proximal regions of the apical dendrite. This suggests that distal regions of the dendrite may remain active independent of NaV1.1-1.3 channel expression, perhaps facilitated by activation of T-type calcium channels and NMDA receptors. By contrast, circuit level reduction of activity by naris occlusion resulted in a global depression of spine number. Together, these results indicate that ABNs retain the ability to develop their typical overall morphological features regardless of experienced activity, and activity modulates the number and location of formed connections.http://journal.frontiersin.org/Journal/10.3389/fnins.2011.00066/fullNeurogenesisSodium ChannelsmorphologyOlfactionactivitynaris occlusion
collection DOAJ
language English
format Article
sources DOAJ
author Jeffrey E Dahlen
Daniel A Jimenez
Daniel A Jimenez
Richard C Gerkin
Richard C Gerkin
Nathan N Urban
Nathan N Urban
Nathan N Urban
spellingShingle Jeffrey E Dahlen
Daniel A Jimenez
Daniel A Jimenez
Richard C Gerkin
Richard C Gerkin
Nathan N Urban
Nathan N Urban
Nathan N Urban
Morphological analysis of activity-reduced adult-born neurons in the mouse olfactory bulb
Frontiers in Neuroscience
Neurogenesis
Sodium Channels
morphology
Olfaction
activity
naris occlusion
author_facet Jeffrey E Dahlen
Daniel A Jimenez
Daniel A Jimenez
Richard C Gerkin
Richard C Gerkin
Nathan N Urban
Nathan N Urban
Nathan N Urban
author_sort Jeffrey E Dahlen
title Morphological analysis of activity-reduced adult-born neurons in the mouse olfactory bulb
title_short Morphological analysis of activity-reduced adult-born neurons in the mouse olfactory bulb
title_full Morphological analysis of activity-reduced adult-born neurons in the mouse olfactory bulb
title_fullStr Morphological analysis of activity-reduced adult-born neurons in the mouse olfactory bulb
title_full_unstemmed Morphological analysis of activity-reduced adult-born neurons in the mouse olfactory bulb
title_sort morphological analysis of activity-reduced adult-born neurons in the mouse olfactory bulb
publisher Frontiers Media S.A.
series Frontiers in Neuroscience
issn 1662-453X
publishDate 2011-05-01
description Adult born neurons are added to the olfactory bulb (OB) throughout life in rodents. While many factors have been identified as regulating the survival and integration of adult-born neurons (ABNs) into existing circuitry, the understanding of how these factors affect ABN morphology and connectivity is limited. Here we compare how cell intrinsic (siRNA knock down of voltage gated sodium channels NaV1.1-1.3) and circuit level (naris occlusion) reductions in activity affect ABN morphology during integration into the OB. We found that both manipulations reduce the number of dendritic spines (and thus likely the number of reciprocal synaptic connections) formed with the surrounding circuitry and inhibited dendritic ramification of ABNs. Further, we identified regions of ABN apical dendrites where the largest and most significant decreases occur following siRNA knock down or naris occlusion. In siRNA knock down cells, reduction of spines is observed in proximal regions of the apical dendrite. This suggests that distal regions of the dendrite may remain active independent of NaV1.1-1.3 channel expression, perhaps facilitated by activation of T-type calcium channels and NMDA receptors. By contrast, circuit level reduction of activity by naris occlusion resulted in a global depression of spine number. Together, these results indicate that ABNs retain the ability to develop their typical overall morphological features regardless of experienced activity, and activity modulates the number and location of formed connections.
topic Neurogenesis
Sodium Channels
morphology
Olfaction
activity
naris occlusion
url http://journal.frontiersin.org/Journal/10.3389/fnins.2011.00066/full
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