Department of Obstetrics and Gynecology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430022, China.
Department of Obstetrics and Gynecology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430022, China.
Biochem Biophys Res Commun. 2020 Jul 5;527(4):915-921. doi: 10.1016/j.bbrc.2020.05.032. Epub 2020 May 16.
The migration and invasion of trophoblasts during early pregnancy in known to play an important role in placental development, which ensures the oxygen and nutrients to the fetus. Accumulating evidences suggest that Delta-Like 4(DLL4)-Notch signaling may be involved in the process of trophoblast regulation. However, the potential role of DLL4-Notch signaling as well as its molecular mechanism in trophoblast controlling has not been fully studied. This study is designed to investigate the effects of DLL4-Notch signaling on trophoblast functions in human extravillous trophoblast cell line, HTR-8/SVneo. The possible molecular mechanism of DLL4-Notch signaling in trophoblast was also explored. We observed that activation of DLL4-Notch signaling enhanced cell migration and invasion ability while blockage of DLL4-Notch signaling impaired. Control of DLL4-Notch signaling did not affect cell viability. The expression of EphrinB2 was regulated by DLL4-Notch signaling. In addition, up-regulation of EphrinB2 resulted in the similar effects on trophoblast cell functions as DLL4-Notch signaling activation. Moreover, activation of DLL4-Notch signaling reversed the negative impact of EphrinB2 knock-down on trophoblasts migration and invasion. Our study suggested that DLL4-Notch signaling involved in the regulation of trophoblast migration and invasion, which may be induced by direct regulation of EphrinB2 expression.
已知滋养层细胞在早期妊娠中的迁移和侵袭在胎盘发育中起着重要作用,这确保了胎儿的氧气和营养供应。越来越多的证据表明,Delta 样配体 4(DLL4)-Notch 信号可能参与滋养层调节过程。然而,DLL4-Notch 信号在滋养层调控中的潜在作用及其分子机制尚未得到充分研究。本研究旨在探讨 DLL4-Notch 信号对人绒毛外滋养层细胞系 HTR-8/SVneo 中滋养层功能的影响。还探索了 DLL4-Notch 信号在滋养层中的可能分子机制。我们观察到 DLL4-Notch 信号的激活增强了细胞迁移和侵袭能力,而 DLL4-Notch 信号的阻断则削弱了这种能力。控制 DLL4-Notch 信号不影响细胞活力。EphrinB2 的表达受 DLL4-Notch 信号调控。此外,上调 EphrinB2 的表达对滋养层细胞功能产生了类似于 DLL4-Notch 信号激活的相似影响。此外,DLL4-Notch 信号的激活逆转了 EphrinB2 敲低对滋养层迁移和侵袭的负面影响。本研究表明,DLL4-Notch 信号参与了滋养层迁移和侵袭的调节,这可能是通过 EphrinB2 表达的直接调节来实现的。