Literature DB >> 11836344

Expression of PDS/Pds, the Pendred syndrome gene, in endometrium.

Koichi Suzuki1, Ines E Royaux, Lorraine A Everett, Atsumi Mori-Aoki, Sayuri Suzuki, Kazuaki Nakamura, Takafumi Sakai, Ryohei Katoh, Shuji Toda, Eric D Green, Leonard D Kohn.   

Abstract

Expression of the Pendred syndrome gene (PDS/Pds) is thought to be responsible for the iodide transport in the thyroid as well as the formation and function of the inner ear. Its mRNA is also expressed in the kidney and placenta. We report here that PDS and its encoded protein (pendrin) are also expressed in the endometrium. The RNA levels of rat PDS in the endometrium and kidney were much higher than those of the thyroid, opposite of the pattern of RNA expression in humans. In human endometrium, pendrin localization changed from the basal to apical surfaces of the epithelium during progression of the menstrual cycle. This suggests a possible role for pendrin in cationic ion transport required to maintain the physiological function of the endometrium. Since there is no evidence of endometrial abnormalities in patients with Pendred syndrome, it suggests the existence of a compensatory mechanisms for pendrin's function in the uterus.

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Year:  2002        PMID: 11836344     DOI: 10.1210/jcem.87.2.8390

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN: 0021-972X            Impact factor:   5.958


  18 in total

1.  Lack of pendrin HCO3- transport elevates vestibular endolymphatic [Ca2+] by inhibition of acid-sensitive TRPV5 and TRPV6 channels.

Authors:  Kazuhiro Nakaya; Donald G Harbidge; Philine Wangemann; Bruce D Schultz; Eric D Green; Susan M Wall; Daniel C Marcus
Journal:  Am J Physiol Renal Physiol       Date:  2007-01-02

2.  Atrophic thyroid follicles and inner ear defects reminiscent of cochlear hypothyroidism in Slc26a4-related deafness.

Authors:  Amiel A Dror; Danielle R Lenz; Shaked Shivatzki; Keren Cohen; Osnat Ashur-Fabian; Karen B Avraham
Journal:  Mamm Genome       Date:  2014-04-24       Impact factor: 2.957

3.  Origins and frequencies of SLC26A4 (PDS) mutations in east and south Asians: global implications for the epidemiology of deafness.

Authors:  H-J Park; S Shaukat; X-Z Liu; S H Hahn; S Naz; M Ghosh; H-N Kim; S-K Moon; S Abe; K Tukamoto; S Riazuddin; M Kabra; R Erdenetungalag; J Radnaabazar; S Khan; A Pandya; S-I Usami; W E Nance; E R Wilcox; S Riazuddin; A J Griffith
Journal:  J Med Genet       Date:  2003-04       Impact factor: 6.318

Review 4.  Transcriptional regulation of the pendrin gene.

Authors:  Julia Rozenfeld; Edna Efrati; Lior Adler; Osnat Tal; Stephen L Carrithers; Seth L Alper; Israel Zelikovic
Journal:  Cell Physiol Biochem       Date:  2011-11-16

Review 5.  Intrinsic regulation of thyroid function by thyroglobulin.

Authors:  Donald F Sellitti; Koichi Suzuki
Journal:  Thyroid       Date:  2014-01-17       Impact factor: 6.568

6.  Pendrin is a novel in vivo downstream target gene of the TTF-1/Nkx-2.1 homeodomain transcription factor in differentiated thyroid cells.

Authors:  Monica Dentice; Cristina Luongo; Antonia Elefante; Raffaele Ambrosio; Salvatore Salzano; Mariastella Zannini; Roberto Nitsch; Roberto Di Lauro; Guido Rossi; Gianfranco Fenzi; Domenico Salvatore
Journal:  Mol Cell Biol       Date:  2005-11       Impact factor: 4.272

7.  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

8.  Localization and functional studies of pendrin in the mouse inner ear provide insight about the etiology of deafness in pendred syndrome.

Authors:  Ines E Royaux; Inna A Belyantseva; Tao Wu; Bechara Kachar; Lorraine A Everett; Daniel C Marcus; Eric D Green
Journal:  J Assoc Res Otolaryngol       Date:  2003-09

9.  Acute regulation of the SLC26A3 congenital chloride diarrhoea anion exchanger (DRA) expressed in Xenopus oocytes.

Authors:  Marina N Chernova; Lianwei Jiang; Boris E Shmukler; Clifford W Schweinfest; Paola Blanco; Steven D Freedman; Andrew K Stewart; Seth L Alper
Journal:  J Physiol       Date:  2003-03-21       Impact factor: 5.182

10.  Two common and three novel PDS mutations in Thai patients with Pendred syndrome.

Authors:  T Snabboon; W Plengpanich; S Saengpanich; S Sirisalipoch; S Keelawat; S Sunthornyothin; W Khovidhunkit; S Suwanwalaikorn; V Sridama; V Shotelersuk
Journal:  J Endocrinol Invest       Date:  2007-12       Impact factor: 4.256

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