Evidence map›Paper›PMID 23261763›Full record

ArticleExperimental neurology2013

Anterograde trafficking of neurotrophin-3 in the adult olfactory system in vivo.

Huan Liu, Michael Lu, Kathleen M Guthrie

Abstract read
In one paragraph

Article in Experimental neurology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
  2. Review
  3. Cellular Diversity and Regeneration in Taste Buds.Current opinion in physiology · 2021
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. 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

3 authors.

Huan LiuDepartment of Basic Biomedical Science, College of Medicine, Florida Atlantic University, Boca Raton, FL 33431, USA.
Michael Lu
Kathleen M Guthrie

Funding

MBRS Support of Continuous Research Excellence at FAUS06GM073621 · NIGMS · FLORIDA ATLANTIC UNIVERSITY · PI NARAYANAN, RAMASWAMY · 2005 to 2008
$3.4M
BDNF over-expression and olfactory neurogenesisR15DC012425 · NIDCD · FLORIDA ATLANTIC UNIVERSITY · PI GUTHRIE, KATHLEEN M · 2012 to 2012
$429k
Trafficking of neurotrophic factors in the forebrain in vivo using viral construcR15DC010485 · NIDCD · FLORIDA ATLANTIC UNIVERSITY · PI GUTHRIE, KATHLEEN M · 2009 to 2009
$215k
NIDCD NIH HHS DC010485NIDCD NIH HHS R15 DC010485NIDCD NIH HHS R15 DC012425NIGMS NIH HHS GM073621NIGMS NIH HHS S06 GM073621
6 · The paper itself

Abstract

The olfactory system continuously incorporates new neurons into functional circuits throughout life. Axons from olfactory sensory neurons (OSNs) in the nasal cavity synapse on mitral, tufted and periglomerular (PG) cells in the main olfactory bulb, and low levels of turnover within the OSN population results in ingrowth of new axons under normal physiological conditions. Subpopulations of bulb interneurons are continually eliminated by apoptosis, and are replaced by new neurons derived from progenitors in the adult forebrain subventricular zone. Integration of new neurons, including PG cells that are contacted by sensory axons, leads to ongoing reorganization of adult olfactory bulb circuits. The mechanisms regulating this adaptive structural plasticity are not all known, but the process is reminiscent of early nervous system development. Neurotrophic factors have well-established roles in controlling neuronal survival and connectivity during development, leading to speculation that trophic interactions between OSNs and their target bulb neurons may mediate some of these same processes in adults. A number of different trophic factors and their cognate receptors are expressed in the adult olfactory pathway. Neurotrophin-3 (NT3) is among these, as reflected by beta-galactosidase expression in transgenic reporter mice expressing lacZ under the NT3 promoter. Using a combination of approaches, including immunocytochemistry, real-time PCR of laser-captured RNA, and adenovirus-mediated gene transfer of NT3 fusion peptides in vivo, we demonstrate that OSNs express and anterogradely transport NT3 to the olfactory bulb. We additionally observe that in mice treated with adenovirus encoding NT3 tagged with hemagglutinin (HA), a subset of bulb neurons expressing the TrkC neurotrophin receptor are immunoreactive for HA, suggesting their acquisition of the fusion peptide from infected sensory neurons. Our results therefore provide evidence that OSNs may serve as an afferent source of trophic signals for the adult mouse olfactory bulb.

Indexed as

AnimalsBrain-Derived Neurotrophic FactorCells, CulturedChlorocebus aethiopsCOS CellsEnzyme-Linked Immunosorbent AssayFemaleFluorescent DyesGanglia, SpinalGreen Fluorescent ProteinsHippocampusIn Vitro TechniquesLaser Capture MicrodissectionMiceMice, Inbred C57BLMicroscopy, ImmunoelectronBrain-Derived Neurotrophic FactorFluorescent DyesGreen Fluorescent ProteinsNerve Tissue ProteinsNeurotrophin 3Recombinant Fusion ProteinsRNA, MessengerSecretogranin II

Identifiers

PMID23261763
PMCPMC3570701

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Registered trials

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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.