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Mouse hypospadias: A critical examination and definition.
Sinclair, Adriane Watkins; Cao, Mei; Shen, Joel; Cooke, Paul; Risbridger, Gail; Baskin, Laurence; Cunha, Gerald R.
Afiliación
  • Sinclair AW; Department of Urology, University of California San Francisco, 400 Parnassus Avenue, Box A610, San Francisco, CA 94143, United States.
  • Cao M; Department of Urology, University of California San Francisco, 400 Parnassus Avenue, Box A610, San Francisco, CA 94143, United States.
  • Shen J; Department of Urology, University of California San Francisco, 400 Parnassus Avenue, Box A610, San Francisco, CA 94143, United States.
  • Cooke P; Department of Physiological Sciences, University of Florida, Gainsville, FL 32610, United States.
  • Risbridger G; Monash Institute of Reproduction and Development, Monash University, Monash Medical Centre, Clayton, Victoria, Australia.
  • Baskin L; Department of Urology, University of California San Francisco, 400 Parnassus Avenue, Box A610, San Francisco, CA 94143, United States.
  • Cunha GR; Department of Urology, University of California San Francisco, 400 Parnassus Avenue, Box A610, San Francisco, CA 94143, United States. Electronic address: gerald.cunha@ucsf.edu.
Differentiation ; 92(5): 306-317, 2016 12.
Article en En | MEDLINE | ID: mdl-27068029
ABSTRACT
Hypospadias is a common malformation whose etiology is based upon perturbation of normal penile development. The mouse has been previously used as a model of hypospadias, despite an unacceptably wide range of definitions for this malformation. The current paper presents objective criteria and a definition of mouse hypospadias. Accordingly, diethylstilbestrol (DES) induced penile malformations were examined at 60 days postnatal (P60) in mice treated with DES over the age range of 12 days embryonic to 20 days postnatal (E12-P20). DES-induced hypospadias involves malformation of the urethral meatus, which is most severe in DES E12-P10, DES P0-P10 and DES P5-P15 groups, and less so or absent in the other treatment groups. A frenulum-like ventral tether between the penis and the prepuce was seen in the most severely affected DES-treated mice. Internal penile morphology was also altered in the DES E12-P10, DES P0-P10 and DES P5-P15 groups (with little effect in the other DES treatment groups). Thus, adverse effects of DES are a function of the period of DES treatment and most severe in the P0-P10 period. In "estrogen mutant mice" (NERKI, ßERKO, αERKO and AROM+) hypospadias was only seen in AROM+ male mice having genetically-engineered elevation is serum estrogen. Significantly, mouse hypospadias was only seen distally at and near the urethral meatus where epithelial fusion events are known to take place and never in the penile midshaft, where urethral formation occurs via an entirely different morphogenetic process.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Pene / Desarrollo Embrionario / Hipospadias / Morfogénesis Tipo de estudio: Prognostic_studies Límite: Animals / Humans / Male Idioma: En Revista: Differentiation Año: 2016 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Pene / Desarrollo Embrionario / Hipospadias / Morfogénesis Tipo de estudio: Prognostic_studies Límite: Animals / Humans / Male Idioma: En Revista: Differentiation Año: 2016 Tipo del documento: Article País de afiliación: Estados Unidos
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