Department of Obstetrics and Gynaecology, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, 999077, China.
Shenzhen Key Laboratory of Fertility Regulation, The University of Hong Kong Shenzhen Hospital, Shenzhen, 518000, China.
Commun Biol. 2022 Oct 7;5(1):1064. doi: 10.1038/s42003-022-04044-x.
Human endometrium undergoes cycles of regeneration in women of reproductive age. The endometrial mesenchymal stromal/stem cells (eMSC) contribute to this process. Notch signaling is essential for homeostasis of somatic stem cells. However, its role in eMSC remains unclear. We show with gain- and loss-of-function experiments that activation of Notch signaling promotes eMSC maintenance, while inhibition induces opposite effect. The activation of Notch signaling better maintains eMSC in a quiescent state. However, these quiescent eMSC can re-enter the cell cycle depending on the Notch and Wnt activities in the microenvironment, suggesting a crosstalk between the two signaling pathways. We further show that the Notch signaling is involved in endometrial remodeling event in a mouse menstrual-like model. Suppression of Notch signaling reduces the proliferation of Notch1 label-retaining stromal cells and delays endometrial repair. Our data demonstrate the importance of Notch signaling in regulating the endometrial stem/progenitor cells in vitro and in vivo.
在育龄女性中,人类子宫内膜经历周期性再生。子宫内膜间质基质/干细胞(eMSC)有助于这一过程。Notch 信号对于体干细胞的稳态至关重要。然而,其在 eMSC 中的作用尚不清楚。我们通过功能获得和功能丧失实验表明,Notch 信号的激活促进 eMSC 的维持,而抑制则诱导相反的效果。Notch 信号的激活能更好地使 eMSC 处于静止状态。然而,这些静止的 eMSC 可以根据微环境中的 Notch 和 Wnt 活性重新进入细胞周期,表明这两种信号通路之间存在串扰。我们进一步表明,Notch 信号参与了小鼠月经样模型中的子宫内膜重塑事件。Notch 信号的抑制减少了 Notch1 标记保留基质细胞的增殖,并延迟了子宫内膜修复。我们的数据表明,Notch 信号在调节体外和体内子宫内膜干细胞/祖细胞方面具有重要作用。