Comparison of Reproductive Function in Female TgMISIIR-TAg Transgenic and Wildtype C57BL/6 Mice

• Published in: Comparative medicine Vol. 69; no. 1; pp. 16 - 21
• Main Authors: Hoyer, Patricia B, Rice, Photini F, Howard, Caitlin C, Koevary, Jennifer W, Dominguez Cooks, Joceline P, Hutchens, Gabrielle V, Chambers, Setsuko K, Craig, Zelieann R, Connolly, Denise C, Barton, Jennifer K
• Format: Journal Article
• Language: English
• Published: United States American Association for Laboratory Animal Science 01.02.2019
• Subjects: Animals; Cyclohexenes - toxicity; Estrus - drug effects; Female; Mice; Mice, Inbred C57BL; Mice, Transgenic; Original Research; Ovarian Follicle - drug effects; Pharmacogenomic Variants; Reproduction - drug effects; Reproduction - genetics; Vinyl Compounds - toxicity
• ISSN: 1532-0820; 2769-819X
• DOI: 10.30802/AALAS-CM-18-000008

Transgenic TgMISIIR-TAg (TAg) mice express the oncogenic virus SV40 in Mullerian epithelial cells. Female TAg mice spontaneously develop epithelial ovarian carcinoma, the most common type of ovarian cancer in women. Female TAg mice are infertile, but the reason has not been determined. We therefore investigated whether female TAg mice undergo puberty, demonstrate follicular development, maintain regular cycles, and ovulate. Ovarian cancers in women commonly develop after menopause. The occupational chemical 4-vinylcyclohexene diepoxide (VCD) accelerates follicle degeneration in the ovaries of rats and mice, causing early ovarian failure. We therefore used VCD dosing of mice to develop an animal model for menopause. The purpose of this study was to characterize reproductive parameters in female TAg mice and to investigate whether the onset of ovarian failure due VCD dosing differed between female TAg and WT C57BL/6 mice. As in WT female mice, TAg female mice underwent puberty (vaginal opening) and developed cyclicity in patterns that were similar between the groups. Vehicle-only TAg mice had fewer ovulations (numbers of corpora lutea) than WT animals. VCD exposure delayed the onset of puberty (day of first estrus) in TAg as compared with WT mice. Morphologic evaluation of ovaries revealed many more degenerating follicles in TAg mice than WT mice, and more VCD-dosed TAg mice were in ovarian failure than VCD-dosed WT mice. These results suggest that despite showing similar onset of sexual maturation, TAg mice have increased follicular degeneration and fewer ovulations than WT. These features may contribute to the inability of female TAg mice to reproduce.