TY - JOUR
T1 - Comparison of Reproductive Function in Female TgMISIIR-TAg Transgenic and Wildtype C57BL/6 Mice
AU - Hoyer, Patricia B.
AU - Rice, Photini F.
AU - Howard, Caitlin C.
AU - Koevary, Jennifer W.
AU - Dominguez Cooks, Joceline P.
AU - Hutchens, Gabrielle V.
AU - Chambers, Setsuko K.
AU - Craig, Zelieann R.
AU - Connolly, Denise C.
AU - Barton, Jennifer K.
N1 - Funding Information: Support for this study was provided in part by a grant from the National Institutes of Health 1R01CA195723, the UACC Support Grant, P30CA023074, the FCCC Core Grant NCI P30 CA006927, as well as charitable donations (to DCC’s laboratory) from the Roberta Dubrow Fund, the Teal Tea Foundation, the Bucks County Board of Associates and the Main Line Board of Associates. The TgMISIIR-TAg mice at Fox Chase are bred, maintained and genotyped with the assistance of the FCCC P30 CA006927-supported Laboratory Animal and Genomic Facilities. Publisher Copyright: © 2019 American Association for Laboratory Animal Science. All right reserved.
PY - 2019/2
Y1 - 2019/2
N2 - 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.
AB - 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.
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U2 - https://doi.org/10.30802/AALAS-CM-18-000008
DO - https://doi.org/10.30802/AALAS-CM-18-000008
M3 - Article
C2 - 30591091
SN - 1532-0820
VL - 69
SP - 16
EP - 21
JO - Comparative medicine
JF - Comparative medicine
IS - 1
ER -