Androgens and mammalian male reproductive tract development
One of the main functions of androgen is in the sexually dimorphic development of the male reproductive tissues. During embryogenesis, androgen determines the morphogenesis of male specific organs, such as the epididymis, seminal vesicle, prostate and penis. Despite the critical function of androgen...
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Veröffentlicht in: | Biochimica et biophysica acta 2015-02, Vol.1849 (2), p.163-170 |
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Sprache: | eng |
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Zusammenfassung: | One of the main functions of androgen is in the sexually dimorphic development of the male reproductive tissues. During embryogenesis, androgen determines the morphogenesis of male specific organs, such as the epididymis, seminal vesicle, prostate and penis. Despite the critical function of androgens in masculinization, the downstream molecular mechanisms of androgen signaling are poorly understood. Tissue recombination experiments and tissue specific androgen receptor (AR) knockout mouse studies have revealed epithelial or mesenchymal specific androgen-AR signaling functions. These findings also indicate that epithelial–mesenchymal interactions are a key feature of AR specific activity, and paracrine growth factor action may mediate some of the effects of androgens. This review focuses on mouse models showing the interactions of androgen and growth factor pathways that promote the sexual differentiation of reproductive organs. Recent studies investigating context dependent AR target genes are also discussed. This article is part of a Special Issue entitled: Nuclear receptors in animal development.
•Androgen dependent development of epididymis, prostate and external genitalia•Phenotypic analyses of various tissue-specific AR KO mice•Androgen regulates male organ masculinization via epithelial–mesenchymal interaction.•Growth factors regulate male organ formation by epithelial–mesenchymal interaction.•Genome-wide analyses for AR target in vivo are prospective to understand AR actions. |
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ISSN: | 1874-9399 0006-3002 1876-4320 |
DOI: | 10.1016/j.bbagrm.2014.05.020 |