Cited by 272Thyroid Disorders and TreatmentsThyroid Cancer Diagnosis and TreatmentChemical Analysis and Environmental Impact

Post-transcriptional regulation of the sodium/iodide symporter by thyrotropin

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Riedel, Claudia, Levy, Orlie, Carrasco, Nancy·2001·Journal of Biological Chemistry

Abstract

The Na(+)/I(-) symporter (NIS) is a key plasma membrane glycoprotein that mediates active I(-) transport in the thyroid gland (Dai, G., Levy, O., and Carrasco, N. (1996) Nature 379, 458-460), the first step in thyroid hormone biogenesis. Whereas relatively little is known about the mechanisms by which thyrotropin (TSH), the main hormonal regulator of thyroid function, regulates NIS activity, post-transcriptional events have been suggested to play a role (Kaminsky, S. M., Levy, O., Salvador, C., Dai, G., and Carrasco, N. (1994) Proc. Natl. Acad. Sci. U. S. A. 91, 3789-3793). Here we show that TSH induces de novo NIS biosynthesis and modulates the long NIS half-life ( approximately 5 days). In addition, we demonstrate that TSH is required for NIS targeting to or retention in the plasma membrane. We further show that NIS is a phosphoprotein and that TSH modulates its phosphorylation pattern. These results provide strong evidence of the major role played by post-transcriptional events in the regulation of NIS by TSH. Beyond their inherent interest, it is also of medical significance that these TSH-dependent regulatory mechanisms may be altered in the large proportion of thyroid cancers in which NIS is predominantly expressed in intracellular compartments, instead of being properly targeted to the plasma membrane.

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  • TSH can increase the half-life of NIS protein and plasma membrane translocation, possibly mediated by TSH-stimulated NIS phosphorylation.

    “It has been demonstrated that TSH can increase the half-life of NIS protein and plasma membrane translocation, which may be mediated by TSH-stimulated NIS phosphorylation (165).”

    From Intrathyroidal feedforward and feedback network regulating thyroid hormone synthesis and secretion (2022) · cites this paper as [165]

    The Results report that NIS half-life was approximately 5 days with TSH versus 3 days without it, and that TSH regulates NIS distribution at the cell surface. The Discussion says TSH is required for targeting NIS to and/or retaining it at the plasma membrane, but explicitly leaves those possibilities unresolved. It also shows TSH-dependent phosphorylation changes while treating a role for phosphorylation in targeting as a question for future investigation, not an established mechanism. (LLM, conf=0.86)

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Research works printed but not linked: 25

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Authors
Riedel, C., Levy, O., & Carrasco, N.
Affiliations
Albert Einstein College of Medicine (US)
Corresponding author
Carrasco, Nancy
Venue
Journal of Biological Chemistry
Publisher
Elsevier BV
Published
2001-06
Volume
276
Issue
24
Pages
21458-21463
ISSN
0021-9258 (ISSN-L)
OpenAlex
W2062536748
Cited by
272
References
0
Citations by year
2026: 7 · 2025: 5 · 2024: 2 · 2023: 5 · 2022: 8 · 2021: 9 · 2020: 6 · 2019: 9 · 2018: 10 · 2017: 13 · 2016: 11 · 2015: 15 · 2014: 11 · 2013: 12 · 2012: 15
FWCI
8.66
Type
journal article
Language
en
Open access
Locations
  • Journal of Biological Chemistry (publishedVersion, cc-by)
  • PubMed (publishedVersion)
Funders
National Institute of Diabetes and Digestive and Kidney Diseases (R01DK041544, DK 07218, DK41544, T32DK007218)
Topics
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Thyroid Disorders and Treatments
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Thyroid Cancer Diagnosis and Treatment
  • Physical Sciences › Environmental Science › Health, Toxicology and Mutagenesis › Chemical Analysis and Environmental Impact
Keywords
sodium iodide symporter, thyroid-stimulating hormone, post-transcriptional regulation, iodide transport, protein phosphorylation, protein half-life, plasma membrane targeting, thyroid cancer
MeSH terms
Sodium-Iodide Symporters, Animals, Biological Transport, Carrier Proteins, Cell Line, Cell Membrane, Half-Life, Iodides, Kinetics, Membrane Proteins, Phosphoproteins, Phosphorylation, Protein Processing, Post-Translational, Thyroid Gland, Thyrotropin, Symporters, Rats

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