Evidence map›Paper›PMID 24378336›Full record

ArticleDevelopmental biology2014

BDNF and NT4 play interchangeable roles in gustatory development.

Tao Huang, Robin F Krimm

Abstract read
In one paragraph

Article in Developmental biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.5field-weighted citation impact, top 20% of its field
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

11 citing papers in PubMed, 16 citations in OpenAlex.

  1. Wiring the senses: Factors that regulate peripheral axon pathfinding in sensory systems.Developmental dynamics : an official publication of the American Association of Anatomists · 2023
    Review
  2. Article
  3. Article
  4. Neurotrophic Factors and Their Potential Applications in Tissue Regeneration.Archivum immunologiae et therapiae experimentalis · 2016
    Review
  5. Article
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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

2 authors at 1 institution in 1 country.

Tao HuangDepartment of Anatomical Sciences and Neurobiology, University of Louisville School of Medicine, Louisville, KY 40292, USA.
Robin F KrimmDepartment of Anatomical Sciences and Neurobiology, University of Louisville School of Medicine, Louisville, KY 40292, USA. Electronic address: rfkrim01@louisville.edu.
University of Louisville · US

Funding

Regulation of taste neuron morphology and functionR01DC007176 · NIDCD · UNIVERSITY OF LOUISVILLE · PI Robin Frances Krimm · 2005 to 2026
$8.1M
Neurotrophin receptor regulation of taste developmentR01DC009418 · NIDCD · UNIVERSITY OF LOUISVILLE · PI KRIMM, ROBIN FRANCES, MINICHIELLO, LILIANA · 2009 to 2012
$1.1M
NIDCD NIH HHS DC007176NIDCD NIH HHS DC009418NIDCD NIH HHS R01 DC007176NIDCD NIH HHS R01 DC009418
6 · The paper itself

Abstract

A limited number of growth factors are capable of regulating numerous developmental processes, but how they accomplish this is unclear. The gustatory system is ideal for examining this issue because the neurotrophins brain-derived neurotrophic factor (BDNF) and neurotrophin-4 (NT4) have different developmental roles although both of them activate the same receptors, TrkB and p75. Here we first investigated whether the different roles of BDNF and NT4 are due to their differences in temporal and spatial expression patterns. Then, we asked whether or not these two neurotrophins exert their unique roles on the gustatory system by regulating different sets of downstream genes. By using Bdnf(Nt4/Nt4) mice, in which the coding region for BDNF is replaced with NT4, we examined whether the different functions of BDNF and NT4 are interchangeable during taste development. Our results demonstrated that NT4 could mediate most of the unique roles of BDNF during taste development. Specifically, caspase-3-mediated cell death, which was increased in the geniculate ganglion in Bdnf(-/-) mice, was rescued in Bdnf(Nt4/Nt4) mice. In BDNF knockout mice, tongue innervation was disrupted, and gustatory axons failed to reach their targets. However, disrupted innervation was rescued and target innervation is normal when NT4 replaced BDNF. Genome wide expression analyses revealed that BDNF and NT4 mutant mice exhibited different gene expression profiles in the gustatory (geniculate) ganglion. Compared to wild type, the expression of differentiation-, apoptosis- and axon guidance-related genes was changed in BDNF mutant mice, which is consistent with their different roles during taste development. However, replacement of BDNF by NT4 rescued these gene expression changes. These findings indicate that the functions of BDNF and NT4 in taste development are interchangeable. Spatial and temporal differences in BDNF and NT4 expression can regulate differential gene expression in vivo and determine their specific roles during development.

Indexed as

Analysis of VarianceAnimalsBrain-Derived Neurotrophic FactorCarbocyaninesGene Expression ProfilingGene Expression Regulation, DevelopmentalGeniculate GanglionImmunohistochemistryLaser Capture MicrodissectionMiceMice, KnockoutMicroarray AnalysisNerve Growth FactorsReal-Time Polymerase Chain ReactionReverse Transcriptase Polymerase Chain ReactionTaste1,1'-dioleyl-3,3,3',3'-tetramethylindocarbocyanineBrain-Derived Neurotrophic FactorCarbocyaninesNerve Growth Factorsneurotrophin 4Brain derived neurotrophic factorGeniculate ganglion neuronsNeurotrophin-4NeurotrophinsTaste

Identifiers

PMID24378336
PMCPMC3950349
OpenAlexW2120534912

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.