Evidence map›Paper›PMID 22634734›Full record

ReviewBiochimica et biophysica acta2013

The deiodinases and the control of intracellular thyroid hormone signaling during cellular differentiation.

Monica Dentice, Alessandro Marsili, Annmarie Zavacki, P Reed Larsen, Domenico Salvatore

Open access · hybridAbstract readReview
In one paragraph

Review in Biochimica et biophysica acta, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
5.7field-weighted citation impact, top 3% 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

60 citing papers in PubMed, 140 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Reducing uncertainties in quantitative adverse outcome pathways by analysis of thyroid hormone in the neonatal rat brain.Toxicological sciences : an official journal of the Society of Toxicology · 2023
    Article
  11. The Physiological Functions and Polymorphisms of Type II Deiodinase.Endocrinology and metabolism (Seoul, Korea) · 2023
    Review
  12. Review
  13. Article
  14. Review
  15. Review
  16. Review
  17. Selenium and selenoproteins in thermogenic adipocytes.Archives of biochemistry and biophysics · 2022
    Review
  18. Thyroid hormone signaling in the intestinal stem cells and their niche.Cellular and molecular life sciences : CMLS · 2022
    Review
  19. Insights into the Mechanism of Human Deiodinase 1.International journal of molecular sciences · 2022
    Article
  20. High rates of (treated) hypothyroidism among chronic migraine patients consulting a specialized headache clinic: are we missing something?Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2022
    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

5 authors at 4 institutions in 2 countries.

Monica DenticeDepartment of Molecular and Clinical Endocrinology and Oncology, University of Naples Federico II, Italy.
Alessandro Marsili
Annmarie Zavacki
P Reed Larsen
Domenico Salvatore
Brigham and Women's Hospital · USCeinge Biotecnologie Avanzate (Italy) · ITHarvard University · USUniversity of Naples Federico II · IT

Funding

PHYSIOLOGY OF THYROID HORMONE-DEPENDENT GENE EXPRESSIONR01DK044128 · NIDDK · BRIGHAM AND WOMEN'S HOSPITAL · PI LARSEN, PHILIP REED, ZAVACKI, ANN M · 1992 to 2018
$6.8M
PHYSIOLOGICAL ROLE OF THYROXINE-BINDING PROTEINSR01DK036256 · NIDDK · BRIGHAM AND WOMEN'S HOSPITAL · PI LARSEN, PHILIP REED · 1986 to 2011
$4.7M
NIDDK NIH HHS DK036256NIDDK NIH HHS DK044128NIDDK NIH HHS R01 DK036256NIDDK NIH HHS R01 DK044128Telethon GGP11185
6 · The paper itself

Abstract

backgroundThyroid hormone influences gene expression in virtually all vertebrates. Its action is initiated by the activation of T4 to T3, an outer ring deiodination reaction that is catalyzed by the type 1 or the type 2 iodothyronine selenodeiodinases (D1 or D2). Inactivation of T4 and T3 occurs via inner ring deiodination catalyzed by the type 3 iodothyronine selenodeiodinases (D3). The T4 concentration is generally quite stable in human plasma, with T3 levels also remaining constant. Deiodinase actions are tightly regulated in both pre- and post-natal life when they are required to make local adjustments of intracellular T3 concentrations in a precise spatio- and temporal manner. Although all the signals governing the dynamic expression of deiodinases in specific cell types are not known, many important regulatory factors have been deciphered. SCOPE OF REVIEW: This review provides striking examples from the recent literature illustrating how the expression of D2 and D3 is finely tuned during maturation of different organs, and how their action play a critical role in different settings to control intracellular T3 availability. MAJOR

conclusionsEmerging evidence indicates that in various cell contexts, D2 and D3 are expressed in a dynamic balance, in which the expression of one enzyme is coordinately regulated with that of the other to tightly control intracellular T3 levels commensurate with cell requirements at that time. GENERAL SIGNIFICANCE: Deiodinases control TH action in a precise spatio-temporal fashion thereby providing a novel mechanism for the local paracrine and autocrine regulation of TH action. This remarkable tissue-specific regulation of intracellular thyroid status remains hidden due to the maintenance of constant circulating TH concentrations by the hypothalamic-pituitary-thyroid axis. This article is part of a Special Issue entitled Thyroid hormone signalling.

Indexed as

AnimalsCell DifferentiationHumansIodide PeroxidaseSignal TransductionThyroid HormonesIodide PeroxidaseThyroid Hormones

Identifiers

PMID22634734
PMCPMC3670672
OpenAlexW2008390809

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.