Yu Yang, Wang Leilei, Liu Tong, Guan Hongbo
Department of Gynecology and Obstetrics, Shengjing Hospital of China Medical University, Shenyang 110004, People's Republic of China.
Department of Gynecology and Obstetrics, Shengjing Hospital of China Medical University, Shenyang 110004, People's Republic of China.
Biochem Biophys Res Commun. 2015 Jul 31;463(3):285-91. doi: 10.1016/j.bbrc.2015.05.052. Epub 2015 May 20.
Preeclampsia is a devastating pregnancy-related syndrome characterized by the onset of hypertension, proteinuria and edema. Insufficient invasion of trophoblasts is well-known to be correlated with preeclampsia development. The present study was performed to investigate the functional role microRNA (miRNA)-204 in trophoblastic invasion in vitro. We here found that the invasive capabilities of BeWo and JEG3 trophoblast-like cells were suppressed by miR-204 mimics, whereas enhanced by its inhibitor. Matrix metalloproteinase-9 (MMP9) was first confirmed to play a role in regulating trophoblast invasion through loss- or gain-of-function experiment. Notably, we demonstrated MMP9 as a direct target of miR-204 in BeWo cells by using the dual-luciferase assay. Moreover, forced overexpression of MMP9 was noted to partly attenuate the inhibitory effects of miR-204 on BeWo cell invasion. Taken together, our study indicates that miR-204 may contribute to the development of preeclampsia by inhibiting trophoblastic invasion, and that MMP9 is involved in miR-204-mediated trophoblast cell invasion. Our study suggests miR-204 as a novel therapeutic target for preeclampsia.
子痫前期是一种严重的妊娠相关综合征,其特征为高血压、蛋白尿和水肿的出现。众所周知,滋养细胞浸润不足与子痫前期的发展相关。本研究旨在探讨微小RNA(miRNA)-204在体外滋养细胞浸润中的功能作用。我们在此发现,miR-204模拟物抑制了BeWo和JEG3滋养层样细胞的侵袭能力,而其抑制剂则增强了这种能力。通过功能丧失或功能获得实验,首次证实基质金属蛋白酶-9(MMP9)在调节滋养细胞侵袭中发挥作用。值得注意的是,我们通过双荧光素酶测定法证明MMP9是BeWo细胞中miR-204的直接靶点。此外,MMP9的强制过表达部分减弱了miR-204对BeWo细胞侵袭的抑制作用。综上所述,我们的研究表明,miR-204可能通过抑制滋养细胞侵袭而促进子痫前期的发展,并且MMP9参与了miR-204介导的滋养细胞侵袭。我们的研究提示miR-204作为子痫前期的一个新的治疗靶点。