Sinclair Adriane Watkins, Cao Mei, Shen Joel, Cooke Paul, Risbridger Gail, Baskin Laurence, Cunha Gerald R
Department of Urology, University of California San Francisco, 400 Parnassus Avenue, Box A610, San Francisco, CA 94143, United States.
Department of Physiological Sciences, University of Florida, Gainsville, FL 32610, United States.
Differentiation. 2016 Dec;92(5):306-317. doi: 10.1016/j.diff.2016.03.004. Epub 2016 Apr 5.
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, βERKO, 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.
尿道下裂是一种常见的畸形,其病因基于正常阴茎发育的紊乱。尽管对这种畸形的定义范围宽得令人难以接受,但小鼠此前一直被用作尿道下裂的模型。本文提出了小鼠尿道下裂的客观标准和定义。相应地,在胚胎12天至出生后20天(E12 - P20)接受己烯雌酚(DES)治疗的小鼠中,于出生后60天(P60)检查DES诱导的阴茎畸形。DES诱导的尿道下裂涉及尿道口畸形,在DES E12 - P10、DES P0 - P10和DES P5 - P15组中最为严重,而在其他治疗组中则较轻或不存在。在受DES影响最严重的小鼠中,可见阴茎与包皮之间有类似系带的腹侧束缚。DES E12 - P10、DES P0 - P10和DES P5 - P15组的阴茎内部形态也发生了改变(其他DES治疗组影响较小)。因此,DES的不良影响是DES治疗时期的函数,在P0 - P10时期最为严重。在“雌激素突变小鼠”(NERKI、βERKO、αERKO和AROM +)中,仅在血清雌激素经基因工程升高的AROM +雄性小鼠中出现尿道下裂。值得注意的是,小鼠尿道下裂仅在已知发生上皮融合事件的尿道口及其附近远端出现,而从未在阴茎中段出现,阴茎中段的尿道形成是通过完全不同的形态发生过程进行的。