Laboratory of Genetics, NIA/NIH-IRP, 251 Bayview blvd, room 10B014, Baltimore, Maryland 21224, USA.
Nat Commun. 2013;4:1843. doi: 10.1038/ncomms2861.
During female reproductive life, ovarian follicle reserve is reduced by maturation and atresia until menopause ensues. Foxo3 is required to maintain the ovarian reserve in mice. Here we show that overexpression of constitutively active FOXO3 can increase ovarian reproductive capacity in mice. We find increased follicle numbers and decreased gonadotropin levels in aging FOXO3-transgenic mice compared with wild-type littermates, suggesting maintenance of a greater ovarian reserve. Based on cumulative progeny in aging animals, we find 31-49% increased fertility in transgenic females. The gene expression profile of Foxo3-/- knockout ovaries appears older than that of wild-type littermates, and the transgene induces a younger-looking profile, restoring much of the wild-type transcriptome. This is the first gain-of-function model of augmented reproductive reserve in mice, thus emphasizing the role of Foxo3 as a guardian of the ovarian follicle pool in mammals and a potential determinant of the onset of menopause.
在女性生殖生命过程中,卵巢卵泡储备通过成熟和闭锁而减少,直到绝经发生。Foxo3 是维持小鼠卵巢储备所必需的。在这里,我们显示过表达组成型激活的 FOXO3 可以增加小鼠的卵巢生殖能力。与野生型同窝仔相比,我们发现衰老的 FOXO3 转基因小鼠的卵泡数量增加,促性腺激素水平降低,提示卵巢储备得到维持。基于衰老动物的累积后代,我们发现转基因雌性的生育能力增加了 31-49%。Foxo3-/- 基因敲除卵巢的基因表达谱比野生型同窝仔更显老,而转基因诱导出更年轻的表型,恢复了大部分野生型转录组。这是在小鼠中增强生殖储备的首个功能获得模型,因此强调了 Foxo3 作为哺乳动物卵巢卵泡库的守护者和绝经发生的潜在决定因素的作用。