Literature DB >> 23562556

Cloning and functional characterization of the mouse sodium-dependent organic anion transporter Soat (Slc10a6).

Gary Grosser1, Daniela Fietz, Sabine Günther, Katharina Bakhaus, Helene Schweigmann, Bernhard Ugele, Ralph Brehm, Ernst Petzinger, Martin Bergmann, Joachim Geyer.   

Abstract

The sodium-dependent organic anion transporter SOAT is a member of the Solute Carrier Family SLC10. In man, this carrier is predominantly expressed in the testis and has transport activity for sulfoconjugated steroid hormones. Here, we report on cloning, expression analysis and functional characterization of the mouse Soat (mSoat) and compare its characteristics with the human SOAT carrier. Quantitative mRNA expression analysis for mSoat in male mice revealed very high expression in lung and further high expression in testis and skin. Immunohistochemical studies showed expression of the mSoat protein in bronchial epithelial cells of the lung, in primary and secondary spermatocytes as well as round spermatids within the seminiferous tubules of the testis, in the epidermis of the skin, and in the urinary epithelium of the bladder. Stably transfected mSoat-HEK293 cells revealed sodium-dependent transport for dehydroepiandrosterone sulfate (DHEAS), estrone-3-sulfate, and pregnenolone sulfate (PREGS) with apparent Km values of 60.3μM, 2.1μM, and 2.5μM, respectively. In contrast to human SOAT, which has a preference for DHEAS as a substrate, mSoat exhibits the highest transport rate for PREGS, likely reflecting differences in the steroid pattern between both species. In conclusion, although certain differences between human SOAT and mSoat exist regarding quantitative gene expression in endocrine and non-endocrine tissues, as well as in the transport kinetics for steroid sulfates, in general, both can be regarded as homologous carriers.
Copyright © 2013 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  DHEAS; Mouse; Pregnenolone sulfate; SOAT; Steroid sulfates; Transport

Mesh:

Substances:

Year:  2013        PMID: 23562556     DOI: 10.1016/j.jsbmb.2013.03.009

Source DB:  PubMed          Journal:  J Steroid Biochem Mol Biol        ISSN: 0960-0760            Impact factor:   4.292


  6 in total

1.  Inflammation-associated upregulation of the sulfated steroid transporter Slc10a6 in mouse liver and macrophage cell lines.

Authors:  Astrid Kosters; Demesew F Abebe; Julio C Felix; Paul A Dawson; Saul J Karpen
Journal:  Hepatol Res       Date:  2015-11-19       Impact factor: 4.288

2.  Transgenerational transmission of asthma risk after exposure to environmental particles during pregnancy.

Authors:  David J Gregory; Lester Kobzik; Zhiping Yang; Connor C McGuire; Alexey V Fedulov
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2017-05-11       Impact factor: 5.464

3.  Role of the Steroid Sulfate Uptake Transporter Soat (Slc10a6) in Adipose Tissue and 3T3-L1 Adipocytes.

Authors:  Emre Karakus; Andreas Schmid; Silke Leiting; Bärbel Fühler; Andreas Schäffler; Thilo Jakob; Joachim Geyer
Journal:  Front Mol Biosci       Date:  2022-04-28

4.  Expression, sorting and transport studies for the orphan carrier SLC10A4 in neuronal and non-neuronal cell lines and in Xenopus laevis oocytes.

Authors:  Stephanie Schmidt; Marcela Moncada; Simone Burger; Joachim Geyer
Journal:  BMC Neurosci       Date:  2015-06-19       Impact factor: 3.288

5.  Estrone-3-Sulfate Stimulates the Proliferation of T47D Breast Cancer Cells Stably Transfected With the Sodium-Dependent Organic Anion Transporter SOAT (SLC10A6).

Authors:  Emre Karakus; Daniel Zahner; Gary Grosser; Regina Leidolf; Cemal Gundogdu; Alberto Sánchez-Guijo; Stefan A Wudy; Joachim Geyer
Journal:  Front Pharmacol       Date:  2018-08-21       Impact factor: 5.810

6.  Substrate Specificities and Inhibition Pattern of the Solute Carrier Family 10 Members NTCP, ASBT and SOAT.

Authors:  Gary Grosser; Simon Franz Müller; Michael Kirstgen; Barbara Döring; Joachim Geyer
Journal:  Front Mol Biosci       Date:  2021-05-17
  6 in total

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