Evidence map›Paper›PMID 27373833›Full record

ArticleNeuron2016

Persistent Structural Plasticity Optimizes Sensory Information Processing in the Olfactory Bulb.

Kurt A Sailor, Matthew T Valley, Martin T Wiechert, Hermann Riecke, Gerald J Sun, Wayne Adams, James C Dennis, Shirin Sharafi, Guo-Li Ming, Hongjun Song and 1 more

Abstract read
In one paragraph

Article in Neuron, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

43 citing papers in PubMed.

  1. Article
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  13. The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Connectivity and dynamics in the olfactory bulb.PLoS computational biology · 2022
    Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Kurt A SailorLaboratory for Perception and Memory, Pasteur Institute, 75015 Paris, France; Centre National de la Recherche Scientifique (CNRS), Unité de Recherche Associée (UMR3571), 75015 Paris, France; Institute for Cell Engineering, Johns Hopkins University School of Medicine, 733 North Broadway, Baltimore, MD 21205, USA; The Solomon Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, 725 N. Wolf Street, Baltimore, MD 21205, USA; Diana Helis Henry Medical Research Foundation, New Orleans, LA 70130-2685, USA.
Matthew T ValleyLaboratory for Perception and Memory, Pasteur Institute, 75015 Paris, France; Centre National de la Recherche Scientifique (CNRS), Unité de Recherche Associée (UMR3571), 75015 Paris, France.
Martin T WiechertLaboratory for Perception and Memory, Pasteur Institute, 75015 Paris, France; Centre National de la Recherche Scientifique (CNRS), Unité de Recherche Associée (UMR3571), 75015 Paris, France.
Hermann RieckeEngineering Science and Applied Mathematics, Northwestern University, Evanston, IL 60208, USA.
Gerald J SunInstitute for Cell Engineering, Johns Hopkins University School of Medicine, 733 North Broadway, Baltimore, MD 21205, USA; The Solomon Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, 725 N. Wolf Street, Baltimore, MD 21205, USA.
Wayne AdamsEngineering Science and Applied Mathematics, Northwestern University, Evanston, IL 60208, USA.
James C DennisEngineering Science and Applied Mathematics, Northwestern University, Evanston, IL 60208, USA.
Shirin SharafiLaboratory for Perception and Memory, Pasteur Institute, 75015 Paris, France; Centre National de la Recherche Scientifique (CNRS), Unité de Recherche Associée (UMR3571), 75015 Paris, France.
Guo-Li MingInstitute for Cell Engineering, Johns Hopkins University School of Medicine, 733 North Broadway, Baltimore, MD 21205, USA; The Solomon Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, 725 N. Wolf Street, Baltimore, MD 21205, USA; Department of Neurology, Johns Hopkins University School of Medicine, 600 N. Wolf Street, Baltimore, MD 21205, USA; Department of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA; Diana Helis Henry Medical Research Foundation, New Orleans, LA 70130-2685, USA.
Hongjun SongInstitute for Cell Engineering, Johns Hopkins University School of Medicine, 733 North Broadway, Baltimore, MD 21205, USA; The Solomon Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, 725 N. Wolf Street, Baltimore, MD 21205, USA; Department of Neurology, Johns Hopkins University School of Medicine, 600 N. Wolf Street, Baltimore, MD 21205, USA; Diana Helis Henry Medical Research Foundation, New Orleans, LA 70130-2685, USA. Electronic address: shongju1@jhmi.edu.
Pierre-Marie LledoLaboratory for Perception and Memory, Pasteur Institute, 75015 Paris, France; Centre National de la Recherche Scientifique (CNRS), Unité de Recherche Associée (UMR3571), 75015 Paris, France. Electronic address: pierre-marie.lledo@pasteur.fr.

Funding

Development of new neurons in the adult brainR01NS047344 · NINDS · JOHNS HOPKINS UNIVERSITY · PI SONG, HONGJUN · 2003 to 2011
$3.4M
Calcium signaling in neuronal navigationR01NS048271 · NINDS · JOHNS HOPKINS UNIVERSITY · PI MING, GUO-LI · 2004 to 2014
$3.2M
Local circuitry mechanisms regulating adult hippocampal neurogenesisR37NS047344 · NINDS · UNIVERSITY OF PENNSYLVANIA · PI SONG, HONGJUN · 2013 to 2019
$2.9M
Circuitry mechanisms underlying normal and aberrant adult hippocampal neurogenesisR01MH105128 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI MING, GUO-LI · 2014 to 2018
$2.0M
Regulation of adult neurogenesis during agingR01AG024984 · NIA · JOHNS HOPKINS UNIVERSITY · PI SONG, HONGJUN · 2004 to 2008
$1.6M
CRCNS US-French Research Proposal Plastic Neural Circuits in Olfactory LearningR01DC015137 · NIDCD · NORTHWESTERN UNIVERSITY · PI RIECKE, HERMANN · 2015 to 2017
$328k
Activity dependent integration of adult born granule cells in the olfactory bulbF31NS066612 · NINDS · JOHNS HOPKINS UNIVERSITY · PI SAILOR, KURT A · 2009 to 2011
$124k
NIA NIH HHS R01 AG024984NIDCD NIH HHS R01 DC015137NIMH NIH HHS R01 MH105128NINDS NIH HHS F31 NS066612NINDS NIH HHS R01 NS047344NINDS NIH HHS R01 NS048271NINDS NIH HHS R37 NS047344
6 · The paper itself

Abstract

In the mammalian brain, the anatomical structure of neural circuits changes little during adulthood. As a result, adult learning and memory are thought to result from specific changes in synaptic strength. A possible exception is the olfactory bulb (OB), where activity guides interneuron turnover throughout adulthood. These adult-born granule cell (GC) interneurons form new GABAergic synapses that have little synaptic strength plasticity. In the face of persistent neuronal and synaptic turnover, how does the OB balance flexibility, as is required for adapting to changing sensory environments, with perceptual stability? Here we show that high dendritic spine turnover is a universal feature of GCs, regardless of their developmental origin and age. We find matching dynamics among postsynaptic sites on the principal neurons receiving the new synaptic inputs. We further demonstrate in silico that this coordinated structural plasticity is consistent with stable, yet flexible, decorrelated sensory representations. Together, our study reveals that persistent, coordinated synaptic structural plasticity between interneurons and principal neurons is a major mode of functional plasticity in the OB.

Indexed as

AnimalsDendritic SpinesInterneuronsMiceNerve NetNeurogenesisNeuronal PlasticityOlfactory BulbPatch-Clamp TechniquesSynapses

Identifiers

PMID27373833
PMCPMC5476833

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.