Activation and inactivation of thyroid hormone by deiodinases: Local action with general consequences
Open accessAbstract
The thyroid hormone plays a fundamental role in the development, growth, and metabolic homeostasis in all vertebrates by affecting the expression of different sets of genes. A group of thioredoxin fold-containing selenoproteins known as deiodinases control thyroid hormone action by activating or inactivating the precursor molecule thyroxine that is secreted by the thyroid gland. These pathways ensure regulation of the availability of the biologically active molecule T3, which occurs in a time-and tissue-specific fashion. In addition, because cells and plasma are in equilibrium and deiodination affects central thyroid hormone regulation, these local deiodinase-mediated events can also affect systemic thyroid hormone economy, such as in the case of non-thyroidal illness. Heightened interest in the field has been generated following the discovery that the deiodinases can be a component in both the Sonic hedgehog signaling pathway and the TGR-5 signaling cascade, a G-protein-coupled receptor for bile acids. These new mechanisms involved in deiodinase regulation indicate that local thyroid hormone activation and inactivation play a much broader role than previously thought.
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In muscle, local conversion of T4 to T3 by DIO2 is important for muscle function both in rodents and in humans.
“In muscle, local conversion of T4 toT3 by DIO2 is important for muscle function both in rodents and in humans [4, 26, 27].”
From An update on non-thyroidal illness syndrome (2021) · cites this paper as [27]
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References 227 · Cited by 207
- Authors
- Gereben, B., Zeöld, A., Dentice, M., Salvatore, D., & Bianco, A. C.
- Affiliations
- HUN-REN Institute of Experimental Medicine (HU)
- University of Naples Federico II (IT)
- Brigham and Women's Hospital (US)
- Corresponding author
- Bianco, A. C.
- Venue
- Cellular and Molecular Life Sciences
- Published
- 2007-11-09
- Volume
- 65
- Issue
- 4
- Pages
- 570-590
- ISSN
- 1420-682X (ISSN-L)
- 1420-9071
- PMC
- PMC11131710
- OpenAlex
- W2047308744
- Semantic Scholar
- 981bc03b004152622e07006c66256fc2e0219506
- Cited by
- 207
- References
- 227
- Citations by year
- 2026: 4 · 2025: 9 · 2024: 8 · 2023: 5 · 2022: 16 · 2021: 10 · 2020: 8 · 2019: 16 · 2018: 12 · 2017: 13 · 2016: 10 · 2015: 12 · 2014: 15 · 2013: 9 · 2012: 10
- FWCI
- 8.80
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Cellular and Molecular Life Sciences (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- American Society for Biochemistry and Molecular Biology
- Fogarty International Center (TW006467, R03TW006467)
- National Institute of Diabetes and Digestive and Kidney Diseases (DK 65055, DK77148, R01DK065055, DK 58538, R01DK077148)
- Topics
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Thyroid Disorders and Treatments
- Health Sciences › Nursing › Nutrition and Dietetics › Selenium in Biological Systems
- Physical Sciences › Environmental Science › Health, Toxicology and Mutagenesis › Chemical Analysis and Environmental Impact
- Keywords
- thyroid hormones, deiodinases, thyroxine, triiodothyronine, selenoproteins, thyroid hormone regulation, low T3 syndrome, Sonic hedgehog signaling, bile acid signaling
- MeSH terms
- Animals, Brain, Cell Membrane, Endoplasmic Reticulum, Enzyme Activation, Humans, Hypothyroidism, Iodide Peroxidase, Kinetics, Models, Molecular, Protein Conformation, Reference Values, Antithyroid Agents, Thyroid Hormones, Polymorphism, Single Nucleotide
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