Evidence map›Paper›PMID 25189772›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2014

Olfactory learning promotes input-specific synaptic plasticity in adult-born neurons.

Gabriel Lepousez, Antoine Nissant, Alex K Bryant, Gilles Gheusi, Charles A Greer, Pierre-Marie Lledo

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers.

0numbers the graph read from it
0cells of the map it votes in
62citing 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

62 citing papers in PubMed.

  1. Article
  2. Observational
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  7. [Application of optogenetic technology in the research on olfactory bulb neural projection from advanced brain regions to regulate olfactory signal processing].Sheng wu yi xue gong cheng xue za zhi = Journal of biomedical engineering = Shengwu yixue gongchengxue zazhi · 2024
    Review
  8. Article
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  12. Review
  13. Article
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  18. Article
  19. Article
  20. Connectivity and dynamics in the olfactory bulb.PLoS computational biology · 2022
    Article

2 more citing papers are in PubMed but not listed here.

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

6 authors.

Gabriel LepousezPerception and Memory Laboratory, Neuroscience Department, Institut Pasteur and Centre National de la Recherche Scientifique Unité Mixte de Recherche 3571, F-75724 Paris, France; gabriel.lepousez@pasteur.fr pierre-marie.lledo@pasteur.fr.
Antoine NissantPerception and Memory Laboratory, Neuroscience Department, Institut Pasteur and Centre National de la Recherche Scientifique Unité Mixte de Recherche 3571, F-75724 Paris, France;
Alex K BryantPerception and Memory Laboratory, Neuroscience Department, Institut Pasteur and Centre National de la Recherche Scientifique Unité Mixte de Recherche 3571, F-75724 Paris, France;
Gilles GheusiPerception and Memory Laboratory, Neuroscience Department, Institut Pasteur and Centre National de la Recherche Scientifique Unité Mixte de Recherche 3571, F-75724 Paris, France; Laboratory of Experimental and Comparative Ethology, University of Paris 13, Sorbonne Paris Cité, F-93430 Villetaneuse, France; and Departments of.
Charles A GreerNeurobiology and Neurosurgery, Yale University School of Medicine, New Haven, CT 06520.
Pierre-Marie LledoPerception and Memory Laboratory, Neuroscience Department, Institut Pasteur and Centre National de la Recherche Scientifique Unité Mixte de Recherche 3571, F-75724 Paris, France; gabriel.lepousez@pasteur.fr pierre-marie.lledo@pasteur.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The production of new neurons in the olfactory bulb (OB) through adulthood is a major mechanism of structural and functional plasticity underlying learning-induced circuit remodeling. The recruitment of adult-born OB neurons depends not only on sensory input but also on the context in which the olfactory stimulus is received. Among the multiple steps of adult neurogenesis, the integration and survival of adult-born neurons are both strongly influenced by olfactory learning. Conversely, optogenetic stimulation of adult-born neurons has been shown to specifically improve olfactory learning and long-term memory. However, the nature of the circuit and the synaptic mechanisms underlying this reciprocal influence are not yet known. Here, we showed that olfactory learning increases the spine density in a region-restricted manner along the dendritic tree of adult-born granule cells (GCs). Anatomical and electrophysiological analysis of adult-born GCs showed that olfactory learning promotes a remodeling of both excitatory and inhibitory inputs selectively in the deep dendritic domain. Circuit mapping revealed that the malleable dendritic portion of adult-born neurons receives excitatory inputs mostly from the regions of the olfactory cortex that project back to the OB. Finally, selective optogenetic stimulation of olfactory cortical projections to the OB showed that learning strengthens these inputs onto adult-born GCs. We conclude that learning promotes input-specific synaptic plasticity in adult-born neurons, which reinforces the top-down influence from the olfactory cortex to early stages of olfactory information processing.

Indexed as

AnimalsDendritesMaleMemory, Long-TermMiceMice, TransgenicNeurogenesisNeuronal PlasticityOlfactory BulbOlfactory Pathwayscortico-bulbar projectionsglutamateinhibitory circuitspiriform cortexsensory systems

Identifiers

PMID25189772
PMCPMC4183341

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.