Du Xingrong, Dong Yongli, Shi Hao, Li Jiang, Kong Shanshan, Shi Donghua, Sun Ling V, Xu Tian, Deng Kejing, Tao Wufan
State Key Laboratory of Genetic Engineering and National Center for International Research of Development and Disease, Institute of Developmental Biology and Molecular Medicine, School of Life Sciences, Fudan University, Shanghai, China.
State Key Laboratory of Genetic Engineering and National Center for International Research of Development and Disease, Institute of Developmental Biology and Molecular Medicine, School of Life Sciences, Fudan University, Shanghai, China; Howard Hughes Medical Institute, Department of Genetics, Yale University School of Medicine, New Haven, Connecticut, United States of America.
PLoS One. 2014 Mar 4;9(3):e90701. doi: 10.1371/journal.pone.0090701. eCollection 2014.
The placenta is essential for survival and growth of the fetus because it promotes the delivery of nutrients and oxygen from the maternal circulation as well as fetal waste disposal. Mst1 and Mst2 (Mst1/2), key components of the mammalian hpo/Mst signaling pathway, encode two highly conserved Ser/Thr kinases and play important roles in the prevention of tumorigenesis and autoimmunity, control of T cell development and trafficking, and embryonic development. However, their functions in placental development are not fully understood, and the underlying cellular and molecular mechanisms remain elusive. Here, we investigated the functions of Mst1/2 in mouse placental development using both conventional and conditional (endothelial) Mst1/2 double knockout mice. We found that the number of trophoblast giant cells dramatically increased while spongiotrophoblast cells almost completely disappeared in Mst1/2 deficient placentas. We showed that Mst1/2 deficiency down regulated the expression of Mash2, which is required for suppressing the differentiation of trophoblast giant cells. Furthermore, we demonstrated that endothelial-specific deletion of Mst1/2 led to impaired placental labyrinthine vasculature and embryonic lethality at E11.5, but neither affected vasculature in yolk sac and embryo proper nor endocardium development. Collectively, our findings suggest that Mst1/2 regulate placental development by control of trophoblast cell differentiation and labyrinthine vasculature at midgestation and Mst1/2 control labyrinth morphogenesis in trophoblast- and fetal endothelial-dependent manners. Thus, our studies have defined novel roles of Mst1/2 in mouse placental development.
胎盘对于胎儿的存活和生长至关重要,因为它促进了母体循环中营养物质和氧气的输送以及胎儿废物的排出。Mst1和Mst2(Mst1/2)是哺乳动物hpo/Mst信号通路的关键组成部分,编码两种高度保守的丝氨酸/苏氨酸激酶,在预防肿瘤发生和自身免疫、控制T细胞发育和运输以及胚胎发育中发挥重要作用。然而,它们在胎盘发育中的功能尚未完全了解,其潜在的细胞和分子机制仍然难以捉摸。在这里,我们使用传统的和条件性(内皮)Mst1/2双敲除小鼠研究了Mst1/2在小鼠胎盘发育中的功能。我们发现,在Mst1/2缺陷的胎盘中,滋养层巨细胞的数量显著增加,而海绵滋养层细胞几乎完全消失。我们表明,Mst1/2缺陷下调了Mash2的表达,而Mash2是抑制滋养层巨细胞分化所必需的。此外,我们证明,内皮特异性缺失Mst1/2会导致胎盘迷路血管受损,并在E11.5时导致胚胎死亡,但既不影响卵黄囊和胚胎本身的血管,也不影响心内膜发育。总的来说,我们的研究结果表明,Mst1/2在妊娠中期通过控制滋养层细胞分化和迷路血管来调节胎盘发育,并且Mst1/2以滋养层和胎儿内皮依赖的方式控制迷路形态发生。因此,我们的研究确定了Mst1/2在小鼠胎盘发育中的新作用。