Lack of accelerated ovarian aging in a follicle-stimulating hormone receptor haploinsufficiency model

Abstract

AbstractFollicle-stimulation hormone (FSH) and FSH receptor (FSHR) signaling is essential for lifelong ovarian and endocrine functions in females. Previous studies have reported thatFshrhaploinsufficiency in female mice led to accelerated ovarian aging, including anticipated progressive fertility decline, irregular estrus cycles, increased follicular atresia and premature ovarian failure at 7 to 9 months of age. Interestingly, these phenotypes resemble key characteristics of human menopause and thusFshrhaploinsufficiency was proposed as a promising research mouse model of menopause. However, theFshrhaploinsufficiency model had not been fully explored, especially at the molecular level. In this study, we characterized the ovarian and endocrine functions of aFshrheterozygous knockout allele that was generated on the C57BL/6 genetic background as part of the Knockout Mouse Project (KOMP). Based on our analyses of these mice using a breeding assay, ovarian tissue histology and serum hormone quantifications (i.e. FSH, AMH, INHA) analyses, the KOMPFshrheterozygous knockout female mice do not show the anticipated phenotypes of ovarian aging in terms of fertility and endocrine function. We further confirmed that the expression ofFshris unaltered in the ovaries of the KOMPFshrheterozygous knockout animals compared to wild-type. Together, our data suggests that the KOMPFshrheterozygous knockout strain does not recapitulate the previously reported ovarian aging phenotypes associated to another model ofFshrhaploinsufficiency.