Literature DB >> 20834201

Absence of primary hypothyroidism and goiter in Slc26a4 (-/-) mice fed on a low iodine diet.

D Calebiro1, P Porazzi, M Bonomi, S Lisi, A Grindati, D De Nittis, L Fugazzola, M Marinò, G Bottà, L Persani.   

Abstract

BACKGROUND: Mutations in the SLC26A4 gene, coding for the anion transporter pendrin, are responsible for Pendred syndrome, characterized by congenital sensorineural deafness and dyshormonogenic goiter. The physiological role of pendrin in the thyroid is still unclear and the lack of a thyroid phenotype in some patients with SLC26A4 mutations and in Slc26a4 (-/-) mice indicate the existence of environmental or individual modifiers able to compensate for pendrin inactivation in the thyroid. Since pendrin can transport iodide in vitro, variations in iodide supply have been claimed to account for the thyroid phenotype associated with pendrin defects. AIM: The Slc26a4 (-/-) mouse model was used to test the hypothesis that iodide supply may influence the penetrance and expressivity of SLC26A4 mutations.
MATERIALS AND METHODS: Slc26a4 (-/-) and (+/+) mice were fed up to 6 months on a standard or low iodine diet and were evaluated for thyroid structural abnormalities or biochemical hypothyroidism.
RESULTS: A 27-fold iodide restriction induced similar modifications in thyroid histology, but no differences in thyroid size, T4 or TSH levels were observed between between Slc26a4 (-/-) and (+/+) mice, either in standard conditions and during iodine restriction.
CONCLUSIONS: Iodide restriction is not able to induce a thyroid phenotype in Slc26a4 (-/-) mice. These experimental data, together with those coming from a review of familial Pendred cases leaving in regions either with low or sufficient iodide supply, support the idea that the expression of thyroid phenotype in Pendred syndrome is more powerfully influenced by individual factors than by dietary iodide.

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Year:  2010        PMID: 20834201     DOI: 10.3275/7262

Source DB:  PubMed          Journal:  J Endocrinol Invest        ISSN: 0391-4097            Impact factor:   4.256


  37 in total

1.  Clinical and molecular analysis of three Mexican families with Pendred's syndrome.

Authors:  O Gonzalez Trevino; O Karamanoglu Arseven; C J Ceballos; V I Vives; R C Ramirez; V V Gomez; G Medeiros-Neto; P Kopp
Journal:  Eur J Endocrinol       Date:  2001-06       Impact factor: 6.664

2.  Pendrin, encoded by the Pendred syndrome gene, resides in the apical region of renal intercalated cells and mediates bicarbonate secretion.

Authors:  I E Royaux; S M Wall; L P Karniski; L A Everett; K Suzuki; M A Knepper; E D Green
Journal:  Proc Natl Acad Sci U S A       Date:  2001-03-27       Impact factor: 11.205

3.  Targeted disruption of mouse Pds provides insight about the inner-ear defects encountered in Pendred syndrome.

Authors:  L A Everett; I A Belyantseva; K Noben-Trauth; R Cantos; A Chen; S I Thakkar; S L Hoogstraten-Miller; B Kachar; D K Wu; E D Green
Journal:  Hum Mol Genet       Date:  2001-01-15       Impact factor: 6.150

4.  Molecular analysis of the Pendred's syndrome gene and magnetic resonance imaging studies of the inner ear are essential for the diagnosis of true Pendred's syndrome.

Authors:  L Fugazzola; D Mannavola; N Cerutti; M Maghnie; F Pagella; P Bianchi; G Weber; L Persani; P Beck-Peccoz
Journal:  J Clin Endocrinol Metab       Date:  2000-07       Impact factor: 5.958

5.  Expression of pendrin and the Pendred syndrome (PDS) gene in human thyroid tissues.

Authors:  J M Bidart; C Mian; V Lazar; D Russo; S Filetti; B Caillou; M Schlumberger
Journal:  J Clin Endocrinol Metab       Date:  2000-05       Impact factor: 5.958

6.  Loss of cochlear HCO3- secretion causes deafness via endolymphatic acidification and inhibition of Ca2+ reabsorption in a Pendred syndrome mouse model.

Authors:  Philine Wangemann; Kazuhiro Nakaya; Tao Wu; Rajanikanth J Maganti; Erin M Itza; Joel D Sanneman; Donald G Harbidge; Sara Billings; Daniel C Marcus
Journal:  Am J Physiol Renal Physiol       Date:  2007-02-13

7.  Pendred syndrome: phenotypic variability in two families carrying the same PDS missense mutation.

Authors:  S Masmoudi; I Charfedine; M Hmani; M Grati; A M Ghorbel; A Elgaied-Boulila; M Drira; J P Hardelin; H Ayadi
Journal:  Am J Med Genet       Date:  2000-01-03

8.  Long-term follow-up in patients with Pendred syndrome: vestibular, auditory and other phenotypes.

Authors:  Makoto Sugiura; Eisuke Sato; Tsutomu Nakashima; Junko Sugiura; Atsushi Furuhashi; Takahiko Yoshino; Atsuo Nakayama; Naoyoshi Mori; Hideki Murakami; Shinji Naganawa
Journal:  Eur Arch Otorhinolaryngol       Date:  2005-03-04       Impact factor: 2.503

9.  Two frequent missense mutations in Pendred syndrome.

Authors:  P Van Hauwe; L A Everett; P Coucke; D A Scott; M L Kraft; C Ris-Stalpers; C Bolder; B Otten; J J de Vijlder; N L Dietrich; A Ramesh; S C Srisailapathy; A Parving; C W Cremers; P J Willems; R J Smith; E D Green; G Van Camp
Journal:  Hum Mol Genet       Date:  1998-07       Impact factor: 6.150

10.  Phenocopies for deafness and goiter development in a large inbred Brazilian kindred with Pendred's syndrome associated with a novel mutation in the PDS gene.

Authors:  P Kopp; O K Arseven; L Sabacan; T Kotlar; J Dupuis; H Cavaliere; C L Santos; J L Jameson; G Medeiros-Neto
Journal:  J Clin Endocrinol Metab       Date:  1999-01       Impact factor: 5.958

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  11 in total

Review 1.  The Sodium/Iodide Symporter (NIS): Molecular Physiology and Preclinical and Clinical Applications.

Authors:  Silvia Ravera; Andrea Reyna-Neyra; Giuseppe Ferrandino; L Mario Amzel; Nancy Carrasco
Journal:  Annu Rev Physiol       Date:  2017-02-10       Impact factor: 19.318

Review 2.  Thyroid iodide efflux: a team effort?

Authors:  Peying Fong
Journal:  J Physiol       Date:  2011-10-10       Impact factor: 5.182

Review 3.  The Renal Physiology of Pendrin-Positive Intercalated Cells.

Authors:  Susan M Wall; Jill W Verlander; Cesar A Romero
Journal:  Physiol Rev       Date:  2020-07-01       Impact factor: 37.312

4.  TSH regulates pendrin membrane abundance and enhances iodide efflux in thyroid cells.

Authors:  Liuska Pesce; Aigerim Bizhanova; Juan Carlos Caraballo; Whitney Westphal; Maria L Butti; Alejandro Comellas; Peter Kopp
Journal:  Endocrinology       Date:  2011-11-22       Impact factor: 4.736

5.  The pendrin anion exchanger gene is transcriptionally regulated by uroguanylin: a novel enterorenal link.

Authors:  Julia Rozenfeld; Osnat Tal; Orly Kladnitsky; Lior Adler; Edna Efrati; Stephen L Carrithers; Seth L Alper; Israel Zelikovic
Journal:  Am J Physiol Renal Physiol       Date:  2011-11-30

Review 6.  The Na+/I- symporter (NIS): mechanism and medical impact.

Authors:  Carla Portulano; Monika Paroder-Belenitsky; Nancy Carrasco
Journal:  Endocr Rev       Date:  2013-12-04       Impact factor: 19.871

7.  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

8.  Influence of dietary iodine deficiency on the thyroid gland in Slc26a4-null mutant mice.

Authors:  Tomoyuki Iwata; Tadao Yoshida; Masaaki Teranishi; Yoshiharu Murata; Yoshitaka Hayashi; Yasuhiko Kanou; Andrew J Griffith; Tsutomu Nakashima
Journal:  Thyroid Res       Date:  2011-06-20

9.  An extremely high dietary iodide supply forestalls severe hypothyroidism in Na+/I- symporter (NIS) knockout mice.

Authors:  Giuseppe Ferrandino; Rachel R Kaspari; Andrea Reyna-Neyra; Nabil E Boutagy; Albert J Sinusas; Nancy Carrasco
Journal:  Sci Rep       Date:  2017-07-13       Impact factor: 4.379

10.  Mutation Screening and Functional Study of SLC26A4 in Chinese Patients with Congenital Hypothyroidism

Authors:  Chang-Run Zhang; Yuan-Ping Shi; Cao-Xu Zhang; Feng Sun; Wen-Jiao Zhu; Rui-Jia Zhang; Ya Fang; Qian-Yue Zhang; Chen-Yan Yan; Ying-Xia Ying; Shuang-Xia Zhao; Huai-Dong Song
Journal:  J Clin Res Pediatr Endocrinol       Date:  2021-09-21
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