Literature DB >> 11182750

Regulation of the sodium iodide symporter by iodide in FRTL-5 cells.

P H Eng1, G R Cardona, M C Previti, W W Chin, L E Braverman.   

Abstract

OBJECTIVE: The acute decrease in iodide organification in the thyroid in response to excess iodide is termed the acute Wolff-Chaikoff effect and normal organification resumes in spite of continued high plasma iodide concentrations (escape from the acute Wolff-Chaikoff effect). We have recently reported that large doses of iodide given to rats chronically decrease the sodium/iodide symporter (NIS) mRNA and protein, suggesting that escape is due to a decrease in NIS and subsequent iodide transport. We have now studied the effect of excess iodide on NIS in FRTL-5 cells to further explore the mechanisms whereby excess iodide decreases NIS.
DESIGN: FRTL-5 cells were employed and were incubated in the presence or absence of various concentrations of iodide. NIS mRNA and protein and the turnover of NIS were assessed.
METHODS: NIS mRNA was measured by Northern analysis, NIS protein by Western analysis and NIS turnover by pulse-chase labeling experiments.
RESULTS: Iodide (10(-) mol/l) had no effect on NIS mRNA in FRTL-5 cells at 24 and 48 h compared with cells cultured in the absence of iodide. However, excess iodide decreased NIS protein by 50% of control values at 24 h and by 70% at 48 h. This effect of iodide was dose dependent. Pulse-chase experiments demonstrated that there was no effect of iodide on new NIS protein synthesis and that the turnover of NIS protein in the presence of iodide was 27% faster than in the absence of added iodide.
CONCLUSIONS: Excess iodide does not decrease NIS mRNA in FRTL-5 cells but does decrease NIS protein, suggesting that in this in vitro thyroid cell model iodide modulates NIS, at least in part, at a post-transcriptional level. This iodide-induced decrease in NIS protein appears to be due, at least partially, to an increase in NIS protein turnover.

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Year:  2001        PMID: 11182750     DOI: 10.1530/eje.0.1440139

Source DB:  PubMed          Journal:  Eur J Endocrinol        ISSN: 0804-4643            Impact factor:   6.664


  20 in total

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2.  Decreased radioiodine uptake of FRTL-5 cells after (131)I incubation in vitro: molecular biological investigations indicate a cell cycle-dependent pathway.

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Review 3.  The biology of the sodium iodide symporter and its potential for targeted gene delivery.

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Review 4.  Recent insights into the cell biology of thyroid angiofollicular units.

Authors:  Ides M Colin; Jean-François Denef; Benoit Lengelé; Marie-Christine Many; Anne-Catherine Gérard
Journal:  Endocr Rev       Date:  2013-01-24       Impact factor: 19.871

5.  Strong association of high urinary iodine with thyroid nodule and papillary thyroid cancer.

Authors:  Fang Wang; Yangang Wang; Luan Wang; Xiuxiu Wang; Chun Sun; Mingzhao Xing; Wenjuan Zhao
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6.  Regulation of thyroid oxidative state by thioredoxin reductase has a crucial role in thyroid responses to iodide excess.

Authors:  Suzana G Leoni; Edna T Kimura; Pilar Santisteban; Antonio De la Vieja
Journal:  Mol Endocrinol       Date:  2011-09-08

7.  Excess iodide induces an acute inhibition of the sodium/iodide symporter in thyroid male rat cells by increasing reactive oxygen species.

Authors:  Alejandro A Arriagada; Eduardo Albornoz; Ma Cecilia Opazo; Alvaro Becerra; Gonzalo Vidal; Carlos Fardella; Luis Michea; Nancy Carrasco; Felipe Simon; Alvaro A Elorza; Susan M Bueno; Alexis M Kalergis; Claudia A Riedel
Journal:  Endocrinology       Date:  2015-01-16       Impact factor: 4.736

8.  The Na+/I- symporter mediates active iodide uptake in the intestine.

Authors:  Juan Pablo Nicola; Cécile Basquin; Carla Portulano; Andrea Reyna-Neyra; Monika Paroder; Nancy Carrasco
Journal:  Am J Physiol Cell Physiol       Date:  2008-12-03       Impact factor: 4.249

9.  Dietary iodide controls its own absorption through post-transcriptional regulation of the intestinal Na+/I- symporter.

Authors:  Juan Pablo Nicola; Andrea Reyna-Neyra; Nancy Carrasco; Ana Maria Masini-Repiso
Journal:  J Physiol       Date:  2012-09-24       Impact factor: 5.182

10.  Iodide excess regulates its own efflux: a possible involvement of pendrin.

Authors:  Jamile Calil-Silveira; Caroline Serrano-Nascimento; Peter Andreas Kopp; Maria Tereza Nunes
Journal:  Am J Physiol Cell Physiol       Date:  2016-01-20       Impact factor: 4.249

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