Department of Biological Science and Technology, National Pingtung University of Science and Technology, Pingtung, Taiwan.
Department of Obstetrics and Gynecology, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung, Taiwan.
Biomed J. 2022 Feb;45(1):179-189. doi: 10.1016/j.bj.2021.01.004. Epub 2021 Jan 16.
Previous studies have demonstrated that high levels of estradiol (E2) impair blastocyst implantation through effects on the endometrium; however, whether high E2 directly affects blastocysts is not well established. The present study sought to clarify the direct impacts of high E2 levels on blastocysts in vitro.
ICR virgin albino mice were used. Using an in-vitro 8-day blastocyst culture model, immunofluorescence staining for the estrogen receptor (ER), blastocyst outgrowth assays, differential staining and TUNEL assays of blastocysts, and embryo transfer, we investigated the main outcomes of exposure to different E2 concentrations (10 to 10 M) in vitro and in vivo.
ERα and ERβ expression were detected in pre-implantation stage embryos. In vitro exposure of blastocysts to 10 M E2 for 24 h followed by 7 days culture in the absence of E2 caused severe inhibition of implantation and post-implantation development. The late adverse effects of E2 on post-implantation development still occurred at concentrations of 10 to 10 M. In addition, blastocyst proliferation was reduced and apoptotic cells were increased following exposure to 10 M E2. Using an in vivo embryo-transfer model, we also showed that treatment with high E2 resulted in fewer implantation sites (38% vs. 72% in control) and greater resorption of implanted blastocysts (81% vs. 38% in control).
Exposure to high E2 concentrations in vitro is deleterious to blastocyst implantation and early post-implantation development, mainly owing to direct impacts of E2 on implanting blastocysts. In clinical assisted reproductive technique (ART), high serum E2 concentrations not only affects the endometrium, but also affects blastocysts directly at the period of implantation.
先前的研究表明,高水平的雌二醇(E2)通过对子宫内膜的影响而损害囊胚着床;然而,高水平的 E2 是否直接影响囊胚尚未得到充分证实。本研究旨在阐明高水平的 E2 对体外囊胚的直接影响。
本研究使用 ICR 处女白化小鼠。通过体外 8 天囊胚培养模型、雌激素受体(ER)的免疫荧光染色、囊胚孵育试验、囊胚的差异染色和 TUNEL 检测以及胚胎移植,我们研究了不同浓度 E2(10-10 M)在体外和体内暴露的主要结局。
在着床前胚胎中检测到 ERα 和 ERβ 的表达。体外将囊胚暴露于 10 M E2 24 小时,然后在无 E2 的情况下培养 7 天,导致着床和植入后发育严重抑制。E2 对植入后发育的晚期不良影响仍发生在 10-10 M 的浓度下。此外,暴露于 10 M E2 后,囊胚增殖减少,凋亡细胞增加。使用体内胚胎移植模型,我们还表明,高 E2 处理导致着床部位减少(对照组为 72%,实验组为 38%),植入囊胚的吸收增加(对照组为 38%,实验组为 81%)。
体外暴露于高浓度 E2 对囊胚着床和早期植入后发育是有害的,主要是由于 E2 对植入囊胚的直接影响。在临床辅助生殖技术(ART)中,高血清 E2 浓度不仅影响子宫内膜,而且在着床期直接影响囊胚。