Evidence map›Paper›PMID 31647533›Full record

ArticleCerebral cortex (New York, N.Y. : 1991)2020

Functional Integration of Neuronal Precursors in the Adult Murine Piriform Cortex.

Bruno Benedetti, Dominik Dannehl, Richard König, Simona Coviello, Christina Kreutzer, Pia Zaunmair, Dominika Jakubecova, Thomas M Weiger, Ludwig Aigner, Juan Nacher and 2 more

Abstract read
In one paragraph

Article in Cerebral cortex (New York, N.Y. : 1991), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing 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

37 citing papers in PubMed.

  1. Review
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  11. Generation of a Dcx-CreERGenesis (New York, N.Y. : 2000) · 2024
    Article
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  13. Review
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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

12 authors.

Bruno BenedettiSpinal Cord Injury and Tissue Regeneration Center Salzburg, 5020 Salzburg, Austria.
Dominik DannehlSpinal Cord Injury and Tissue Regeneration Center Salzburg, 5020 Salzburg, Austria.
Richard KönigSpinal Cord Injury and Tissue Regeneration Center Salzburg, 5020 Salzburg, Austria.
Simona CovielloBIOTECMED, Universitat de València and Center for Collaborative Research on Mental Health CIBERSAM, 46100 València, Spain.
Christina KreutzerSpinal Cord Injury and Tissue Regeneration Center Salzburg, 5020 Salzburg, Austria.
Pia ZaunmairSpinal Cord Injury and Tissue Regeneration Center Salzburg, 5020 Salzburg, Austria.
Dominika JakubecovaSpinal Cord Injury and Tissue Regeneration Center Salzburg, 5020 Salzburg, Austria.
Thomas M WeigerDepartment of Biosciences, University of Salzburg, 5020 Salzburg, Austria.
Ludwig AignerSpinal Cord Injury and Tissue Regeneration Center Salzburg, 5020 Salzburg, Austria.
Juan NacherBIOTECMED, Universitat de València and Center for Collaborative Research on Mental Health CIBERSAM, 46100 València, Spain.
Maren EngelhardtInstitute of Neuroanatomy, CBTM, Medical Faculty Mannheim, Heidelberg University, 68167 Mannheim, Germany.
Sébastien Couillard-DesprésSpinal Cord Injury and Tissue Regeneration Center Salzburg, 5020 Salzburg, Austria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The extent of functional maturation and integration of nonproliferative neuronal precursors, becoming neurons in the adult murine piriform cortex, is largely unexplored. We thus questioned whether precursors eventually become equivalent to neighboring principal neurons or whether they represent a novel functional network element. Adult brain neuronal precursors and immature neurons (complex cells) were labeled in transgenic mice (DCX-DsRed and DCX-CreERT2 /flox-EGFP), and their cell fate was characterized with patch clamp experiments and morphometric analysis of axon initial segments. Young (DCX+) complex cells in the piriform cortex of 2- to 4-month-old mice received sparse synaptic input and fired action potentials at low maximal frequency, resembling neonatal principal neurons. Following maturation, the synaptic input detected on older (DCX-) complex cells was larger, but predominantly GABAergic, despite evidence of glutamatergic synaptic contacts. Furthermore, the rheobase current of old complex cells was larger and the maximal firing frequency was lower than those measured in neighboring age-matched principal neurons. The striking differences between principal neurons and complex cells suggest that the latter are a novel type of neuron and new coding element in the adult brain rather than simple addition or replacement for preexisting network components.

Indexed as

AnimalsCell DifferentiationDoublecortin ProteinGene Expression Regulation, DevelopmentalMiceMice, TransgenicMicrotubule-Associated ProteinsNeural Stem CellsNeurogenesisNeuronsNeuropeptidesPiriform CortexDcx protein, mouseDoublecortin ProteinMicrotubule-Associated ProteinsNeuropeptidesadult neurogenesisaxon initial segmentcomplex cellsdoublecortintangled cells

Identifiers

PMID31647533
PMCPMC7132906

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.