McGill University Health CentreMontreal, Quebec, Canada.
Division of Experimental MedicineMcGill University, Montreal, Quebec, Canada.
Reproduction. 2018 Jan;155(1):93-102. doi: 10.1530/REP-17-0436. Epub 2017 Oct 24.
Six members of the Wnt family are expressed in the female reproductive tract. Their collective function ensures proper development of the uterus, preparing it for pregnancy during adulthood. Here, we take advantage of the fact that a prerequisite for all Wnt secretion, is located on the X chromosome, to generate females that were mosaic for throughout the reproductive tract. females were mated with progesterone receptor ()-Cre males ( ) to generate females that were heterozygous for Porcupine in all tissues of the female reproductive tract, resulting in mosaicism due to random X-inactivation. We demonstrated that mosaic females are extremely subfertile and exhibit a large spectrum of phenotypes ranging from morphologically normal uteri to uteri with extremely enlarged cystic glands. Decreased fertility in Porcupine mosaic females was not associated with phenotype severity and was observed regardless of whether or not cystic glands were enlarged. By crossing-in a GFP reporter on the wild-type X chromosome, we were able to correlate endometrial gland hyperplasia with a mostly mutant stroma, demonstrating the role of stromal Wnts in the regulation of endometrial gland proliferation. Finally, we demonstrated that fertility issues within mosaic females were due to a reduced response to estrogen and to abnormal Tcf/Lef signaling across the mesometrial-anti-mesometrial axis during the window of implantation.
Wnt 家族的六个成员在女性生殖道中表达。它们的集体功能确保了子宫的正常发育,为成年后的怀孕做好准备。在这里,我们利用这样一个事实,即所有 Wnt 分泌的前提条件都位于 X 染色体上,从而产生了整个生殖道都存在 Wnt 分泌缺陷的雌性嵌合体。这些 雌性与孕激素受体 ( )-Cre 雄性 ( ) 交配,以产生所有雌性生殖道组织中 Porcupine 杂合的雌性,由于随机 X 染色体失活而导致嵌合体。我们证明,Porcupine 嵌合体雌性的生育能力极低,并表现出从形态正常的子宫到子宫囊性腺极度增大的广泛表型范围。Porcupine 嵌合体雌性的生育力下降与表型严重程度无关,无论囊性腺是否增大都观察到这种情况。通过在野生型 X 染色体上交叉引入 GFP 报告基因,我们能够将子宫内膜腺增生与主要为 突变的基质相关联,证明了基质 Wnt 在调节子宫内膜腺增生中的作用。最后,我们证明了嵌合体雌性的生育问题是由于对雌激素的反应降低以及在植入窗口期间沿系膜-反系膜轴的 Tcf/Lef 信号异常所致。