Your browser doesn't support javascript.
loading
Mice lacking ß-carotene-15,15'-dioxygenase exhibit reduced serum testosterone, prostatic androgen receptor signaling, and prostatic cellular proliferation.
Smith, Joshua W; Ford, Nikki A; Thomas-Ahner, Jennifer M; Moran, Nancy E; Bolton, Eric C; Wallig, Matthew A; Clinton, Steven K; Erdman, John W.
Afiliación
  • Smith JW; Division of Nutritional Sciences, University of Illinois at Urbana-Champaign, Urbana, Illinois.
  • Ford NA; Division of Nutritional Sciences, University of Illinois at Urbana-Champaign, Urbana, Illinois.
  • Thomas-Ahner JM; Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio.
  • Moran NE; Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio.
  • Bolton EC; Department of Molecular and Integrative Physiology, University of Illinois at Urbana-Champaign, Urbana, Illinois.
  • Wallig MA; Division of Nutritional Sciences, University of Illinois at Urbana-Champaign, Urbana, Illinois.
  • Clinton SK; Department of Veterinary Pathobiology, University of Illinois at Urbana-Champaign, Urbana, Illinois.
  • Erdman JW; Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio.
Am J Physiol Regul Integr Comp Physiol ; 311(6): R1135-R1148, 2016 12 01.
Article en En | MEDLINE | ID: mdl-27629887
ß-Carotene-15,15'-dioxygenase (BCO1) cleaves dietary carotenoids at the central 15,15' double bond, most notably acting on ß-carotene to yield retinal. However, Bco1 disruption also impacts diverse physiological end points independent of dietary carotenoid feeding, including expression of genes controlling androgen metabolism. Using the Bco1-/- mouse model, we sought to probe the effects of Bco1 disruption on testicular steroidogenesis, prostatic androgen signaling, and prostatic proliferation. Male wild-type (WT) and Bco1-/- mice were raised on carotenoid-free AIN-93G diets before euthanasia between 10 and 14 wk of age. Weights of the prostate and seminal vesicles were significantly lower in Bco1-/- than in WT mice (-18% and -29%, respectively). Serum testosterone levels in Bco1-/- mice were significantly reduced by 73%. Bco1 disruption significantly reduced Leydig cell number and decreased testicular mRNA expression of Hsd17b3, suggesting inhibition of testicular testosterone synthesis. Immunofluorescent staining of the androgen receptor (AR) in the dorsolateral prostate lobes of Bco1-/- mice revealed a decrease in AR nuclear localization. Analysis of prostatic morphology suggested decreases in gland size and secretion. These findings were supported by reduced expression of the proliferation marker Ki-67 in Bco1-/- prostates. Expression analysis of 200 prostate cancer- and androgen-related genes suggested that Bco1 loss significantly disrupted prostatic androgen receptor signaling, cell cycle progression, and proliferation. This is the first demonstration that Bco1 disruption lowers murine circulating testosterone levels and thereby reduces prostatic androgen receptor signaling and prostatic cellular proliferation, further supporting the role of this protein in processes more diverse than carotenoid cleavage.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Próstata / Testosterona / Receptores Androgénicos / Beta-Caroteno 15,15'-Monooxigenasa Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Am J Physiol Regul Integr Comp Physiol Asunto de la revista: FISIOLOGIA Año: 2016 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Próstata / Testosterona / Receptores Androgénicos / Beta-Caroteno 15,15'-Monooxigenasa Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Am J Physiol Regul Integr Comp Physiol Asunto de la revista: FISIOLOGIA Año: 2016 Tipo del documento: Article Pais de publicación: Estados Unidos