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The glucocorticoid-activating enzyme 11ß-hydroxysteroid dehydrogenase type 1 catalyzes the activation of testosterone.
Oestlund, Imken; Snoep, Jacky; Schiffer, Lina; Wabitsch, Martin; Arlt, Wiebke; Storbeck, Karl-Heinz.
Afiliação
  • Oestlund I; Department of Biochemistry, Stellenbosch University, Stellenbosch, South Africa.
  • Snoep J; Department of Biochemistry, Stellenbosch University, Stellenbosch, South Africa; Molecular Cell Biology, Vrije Universiteit Amsterdam, Amsterdam, the Netherlands.
  • Schiffer L; Institute of Metabolism and Systems Research, University of Birmingham, Birmingham, UK.
  • Wabitsch M; Division of Pediatric Endocrinology and Diabetes, University Hospital of Ulm, Ulm, Germany.
  • Arlt W; Institute of Metabolism and Systems Research, University of Birmingham, Birmingham, UK; Institute of Clinical Sciences, Faculty of Medicine, Imperial College, London, UK; Medical Research Council Laboratory of Medical Sciences, London, UK.
  • Storbeck KH; Department of Biochemistry, Stellenbosch University, Stellenbosch, South Africa; Institute of Metabolism and Systems Research, University of Birmingham, Birmingham, UK. Electronic address: storbeck@sun.ac.za.
J Steroid Biochem Mol Biol ; 236: 106436, 2024 02.
Article em En | MEDLINE | ID: mdl-38035948
Testosterone biosynthesis from its precursor androstenedione is thought to be exclusively catalysed by the 17ß-hydroxysteroid dehydrogenases-HSD17B3 in testes, and AKR1C3 in the ovary, adrenal and peripheral tissues. Here we show for the first time that the glucocorticoid activating enzyme 11ß-hydroxysteroid dehydrogenase type 1 (HSD11B1) can also catalyse the 17ß-reduction of androstenedione to testosterone, using a combination of in vitro enzyme kinetic assays, mathematical modelling, and molecular docking analysis. Furthermore, we show that co-expression of HSD11B1 and AKR1C3 increases testosterone production several-fold compared to the rate observed with AKR1C3 only, and that HSD11B1 is likely to contribute significantly to testosterone production in peripheral tissues.
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Testosterona / Androstenodiona Limite: Female / Humans Idioma: En Revista: J Steroid Biochem Mol Biol Assunto da revista: BIOLOGIA MOLECULAR / BIOQUIMICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: África do Sul

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Testosterona / Androstenodiona Limite: Female / Humans Idioma: En Revista: J Steroid Biochem Mol Biol Assunto da revista: BIOLOGIA MOLECULAR / BIOQUIMICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: África do Sul