McNanley Anna R, Johnson Aimee M, Flynn Michael K, Wood Ronald W, Kennedy Scott D, Reeder Jay E
Department of Obstetrics and Gynecology, University of Rochester Medical Center, 601 Elmwood Avenue, PO Box 668, Rochester, NY 14642, USA.
Int Urogynecol J Pelvic Floor Dysfunct. 2009 Jan;20(1):19-25. doi: 10.1007/s00192-008-0723-7. Epub 2008 Sep 19.
The objective of this study was to report the initial anatomic, radiographic, and genetic evaluations of a novel form of spontaneous pelvic organ prolapse (S-POP) in mice. We observed S-POP in a colony of UPII-SV40T transgenic mice developed for studies on bladder cancer. We utilized magnetic resonance imaging and necropsy to characterize this finding. We have established a breeding colony to identify inheritance patterns and for future studies. Selective breeding isolated the S-POP phenotype from the transgene. In contrast to other animal models, the S-POP mouse does not require an obligatory antecedent event to manifest pelvic organ prolapse. Necropsy and imaging demonstrate significant displacement of the pelvic organs distal to the pelvic floor in both sexes. The appearance of the POP is similar to that seen in the human female phenotype. Preliminary breeding studies indicate an autosomal dominant inheritance pattern. This mouse may be an effective animal model for the study of POP in humans.
本研究的目的是报告对小鼠中一种新型自发性盆腔器官脱垂(S-POP)的初步解剖学、影像学和遗传学评估。我们在为膀胱癌研究培育的UPII-SV40T转基因小鼠群体中观察到了S-POP。我们利用磁共振成像和尸检来描述这一发现。我们建立了一个繁殖群体以确定遗传模式并用于未来的研究。选择性育种将S-POP表型与转基因分离。与其他动物模型不同,S-POP小鼠表现出盆腔器官脱垂不需要特定的先前事件。尸检和成像显示两性中盆腔器官在盆底远端均有明显移位。POP的外观与人类女性表型中所见相似。初步育种研究表明其为常染色体显性遗传模式。这种小鼠可能是研究人类POP的有效动物模型。