Evidence map›Paper›PMID 31513589›Full record

ArticlePloS one2019

Ontogenetic expression of thyroid hormone signaling genes: An in vitro and in vivo species comparison.

Kyla M Walter, Katharina Dach, Keri Hayakawa, Susanne Giersiefer, Heike Heuer, Pamela J Lein, Ellen Fritsche

Open access · goldAbstract readComparative Study
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.4field-weighted citation impact, top 17% 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

12 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Risk Factors from Pregnancy to Adulthood in Multiple Sclerosis Outcome.International journal of molecular sciences · 2022
    Review
  10. Article
  11. Article
  12. Review
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

7 authors at 2 institutions in 2 countries.

Kyla M WalterDepartment of Molecular Biosciences, University of California-Davis, School of Veterinary Medicine, Davis, CA, United States of America.ORCID 0000-0001-5420-3813
Katharina DachIUF-Leibniz Research Institute for Environmental Medicine, Dusseldorf, Germany.
Keri HayakawaDepartment of Molecular Biosciences, University of California-Davis, School of Veterinary Medicine, Davis, CA, United States of America.
Susanne GiersieferIUF-Leibniz Research Institute for Environmental Medicine, Dusseldorf, Germany.
Heike HeuerIUF-Leibniz Research Institute for Environmental Medicine, Dusseldorf, Germany.
Pamela J LeinDepartment of Molecular Biosciences, University of California-Davis, School of Veterinary Medicine, Davis, CA, United States of America.
Ellen FritscheIUF-Leibniz Research Institute for Environmental Medicine, Dusseldorf, Germany.ORCID 0000-0002-7454-679X
Leibniz Institute of Environmental Medicine · DEUniversity of California, Davis · US

Funding

ENVIRONMENTAL TOXICOLOGYT32ES007059 · NIEHS · UNIVERSITY OF CALIFORNIA DAVIS · PI Laura S Van Winkle · 1985 to 2026
$7.9M
NIEHS NIH HHS T32 ES007059
6 · The paper itself

Abstract

Thyroid hormone (TH) is essential for brain development. While disruption of TH signaling by environmental chemicals has been discussed as a mechanism of developmental neurotoxicity (DNT) for more than a decade, there remains a paucity of information linking specific TH disrupting chemicals to adverse neurodevelopmental outcomes. This data gap reflects, in part, the fact that the molecular machinery of TH signaling is complex and varies according to cell type and developmental time. Thus, establishing a baseline of the ontogenetic profile of expression of TH signaling molecules in relevant cell types is critical for developing in vitro and alternative systems-based models for screening TH disrupting chemicals for DNT. Here, we characterize the transcriptomic profile of molecules critical to TH signaling across three species-human, rat, and zebrafish-in vitro and in vivo across different stages of neurodevelopment. Our data indicate that while cultured human and rat neural progenitor cells, primary cultures of rat cortical cells, and larval zebrafish all express a fairly comprehensive transcriptome of TH signaling molecules, the spatiotemporal expression profiles as well as the responses to TH vary across species and developmental stages. The data presented here provides a roadmap for identifying appropriate in vitro and in simpler systems-based models for mechanistic studies and screening of chemicals that alter neurodevelopment via interference with TH action.

Indexed as

Gene Regulatory NetworksAnimalsCells, CulturedFemaleGene Expression ProfilingGene Expression Regulation, DevelopmentalHumansIn Vitro TechniquesLarvaMaleNeurogenesisOptogeneticsPrimary Cell CultureRatsSignal TransductionThyroid HormonesThyroid HormonesZebrafish Proteins

Identifiers

PMID31513589
PMCPMC6742404
OpenAlexW2972528694

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.