College of Animal Science, Zhejiang University, 866 Yuhangtang Road, 310058, Hangzhou, P. R. China.
Zhejiang Animal Husbandry Techniques Extension Station, 310020, Hangzhou, P. R. China.
Reprod Biol Endocrinol. 2021 Jan 7;19(1):2. doi: 10.1186/s12958-020-00689-7.
The establishment of uterine receptivity is essential for embryo implantation initiation and involves a significant morphological transformation in the endometrial epithelial cells (EECs). The remodeling of junctional complexes and membrane-associated cytoskeleton is crucial for epithelial transformation. However, little is known about how this process is regulated in EECs during the receptive phase. ARHGAP19 is a Rho GTPase-activating protein that participates in various cytoskeletal-related events, including epithelial morphogenesis. Here, we investigated the role of ARHGAP19 in endometrial epithelial transformation during the establishment of uterine receptivity. The upstream regulator of ARHGAP19 was also investigated.
ARHGAP19 expression was examined in mouse uteri during early pregnancy and in human EEC lines. The role of ARHGAP19 was investigated by manipulating its expression in EECs. The effect of ARHGAP19 on junctional proteins in EECs was examined by western blotting and immunofluorescence. The effect of ARHGAP19 on microvilli was examined by scanning electron microscopy. The upstream microRNA (miRNA) was predicted using online databases and validated by the dual-luciferase assay. The in vivo and in vitro effect of miRNA on endogenous ARHGAP19 was examined by uterine injection of miRNA agomirs and transfection of miRNA mimics or inhibitors.
ARHGAP19 was upregulated in the receptive mouse uteri and human EECs. Overexpression of ARHGAP19 in non-receptive EECs downregulated the expression of junctional proteins and resulted in their redistribution. Meanwhile, upregulating ARHGAP19 reorganized the cytoskeletal structure of EECs, leading to a decline of microvilli and changes in cell configuration. These changes weakened epithelial cell polarity and promoted the transition of non-receptive EECs to a receptive phenotype. Besides, miR-192-5p, a miRNA that plays a key role in maintaining epithelial properties, was validated as an upstream regulator of ARHGAP19.
These results suggested that ARHGAP19 may contribute to the transition of EECs from a non-receptive to a receptive state by regulating the remodeling of junctional proteins and membrane-associated cytoskeleton.
胚胎着床启动的关键是子宫接受性的建立,这涉及到子宫内膜上皮细胞(EECs)的显著形态转变。连接复合体和膜相关细胞骨架的重塑对于上皮细胞转化至关重要。然而,对于接受期 EEC 中这一过程是如何被调控的,我们知之甚少。ARHGAP19 是一种 Rho GTPase 激活蛋白,参与包括上皮形态发生在内的各种细胞骨架相关事件。在这里,我们研究了 ARHGAP19 在子宫接受性建立过程中对子宫内膜上皮细胞转化的作用。还研究了 ARHGAP19 的上游调节因子。
在早孕小鼠子宫和人 EEC 系中检测 ARHGAP19 的表达。通过在 EEC 中操纵其表达来研究 ARHGAP19 的作用。通过 Western blot 和免疫荧光法检测 ARHGAP19 对 EEC 中连接蛋白的影响。通过扫描电子显微镜观察 ARHGAP19 对微绒毛的影响。使用在线数据库预测上游 microRNA(miRNA),并通过双荧光素酶测定进行验证。通过 miRNA 激动剂子宫内注射和 miRNA 模拟物或抑制剂转染,研究 miRNA 对内源性 ARHGAP19 的体内和体外作用。
ARHGAP19 在接受性小鼠子宫和人 EEC 中上调。在非接受性 EEC 中过表达 ARHGAP19 会下调连接蛋白的表达并导致其重新分布。同时,上调 ARHGAP19 重组 EEC 的细胞骨架结构,导致微绒毛减少和细胞形态改变。这些变化削弱了上皮细胞极性,促进了非接受性 EEC 向接受性表型的转变。此外,miR-192-5p,一种在维持上皮特性中起关键作用的 miRNA,被验证为 ARHGAP19 的上游调节因子。
这些结果表明,ARHGAP19 可能通过调节连接蛋白和膜相关细胞骨架的重塑,促进 EEC 从非接受状态向接受状态的转变。