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卵巢甾体激素和胚胎刺激对 E-钙黏蛋白和 N-钙黏蛋白的调节。

Modulation of E-Cadherin and N-Cadherin by ovarian steroids and embryonic stimuli.

机构信息

Molecular and Cellular Biology Laboratory, ICMR-National Institute for Research in Reproductive Health, Indian Council of Medical Research (ICMR), JM Street, Parel, Mumbai, 400012, India.

Molecular and Cellular Biology Laboratory, ICMR-National Institute for Research in Reproductive Health, Indian Council of Medical Research (ICMR), JM Street, Parel, Mumbai, 400012, India.

出版信息

Tissue Cell. 2021 Dec;73:101670. doi: 10.1016/j.tice.2021.101670. Epub 2021 Oct 21.

DOI:10.1016/j.tice.2021.101670
PMID:34710830
Abstract

Endometrium is a dynamic tissue that undergoes extensive remodelling to attain a receptive state which is further modulated in presence of an embryo for successful initiation of pregnancy. Cadherins are the proteins of the junctional complex of which E-cadherin (E-Cad) is crucial for maintaining epithelial cell state and integrity of the epithelial barrier; gain of N-cadherin (N-Cad) in epithelial cells leads to epithelial to mesenchymal transition (EMT). In the present study, we investigated the expression of E-Cad and N-Cad in the mouse endometrial luminal epithelium and its modulation by estrogen, progesterone, and embryonic stimuli. We observed that E-Cad is diffusely expressed in the luminal epithelium of mouse endometrium during the estrus stage and upon estrogen treatment. It is apico-laterally and basolaterally sorted at the diestrus stage and in response to the combined treatment of estrogen and progesterone. In 3D spheroids of human endometrial epithelial cells, combined treatment with estrogen and progesterone led to lateral sorting of E-Cad without any effects on its mRNA levels. at the time of embryo implantation, there is loss of E-Cad along with the gain of N-Cad and SNAIL expression suggestive of EMT in the luminal epithelium. This EMT is possibly driven by embryonic stimuli as treatment with estrogen and progesterone did not lead to the gain of N-Cad expression in the mouse endometrium in vivo or in human endometrial epithelial cells in vitro. In conclusion, the present study demonstrates that steroid hormones directly affect E-Cad sorting in the endometrial epithelium which undergo EMT in response to embryonic stimuli.

摘要

子宫内膜是一种具有广泛重塑能力的动态组织,通过重塑使其处于接受状态,在胚胎存在的情况下进一步调节,以成功启动妊娠。钙黏蛋白是连接复合体的蛋白,其中 E-钙黏蛋白(E-Cad)对于维持上皮细胞状态和上皮屏障的完整性至关重要;上皮细胞中 N-钙黏蛋白(N-Cad)的获得导致上皮细胞向间充质转化(EMT)。在本研究中,我们研究了 E-Cad 和 N-Cad 在小鼠子宫内膜腔上皮中的表达及其受雌激素、孕激素和胚胎刺激的调节。我们观察到,在发情期和雌激素处理期间,E-Cad 在小鼠子宫内膜的腔上皮中广泛表达。在发情期,E-Cad 在腔上皮的顶-侧和基底-侧被分拣;在孕激素处理下,E-Cad 在腔上皮中被分拣到基底-侧。在人类子宫内膜上皮细胞的 3D 球体中,雌激素和孕激素的联合处理导致 E-Cad 的侧向分拣,而对其 mRNA 水平没有影响。在胚胎着床时,E-Cad 的丢失伴随着 N-Cad 和 SNAIL 表达的增加,提示腔上皮发生 EMT。这种 EMT 可能是由胚胎刺激驱动的,因为雌激素和孕激素处理在体内不会导致小鼠子宫内膜或体外培养的人子宫内膜上皮细胞中 N-Cad 表达的增加。总之,本研究表明,甾体激素直接影响子宫内膜上皮细胞中 E-Cad 的分拣,这种分拣会在胚胎刺激下发生 EMT。

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