Long Jing, Huang Yan, Tang Zhengshan, Shan Yali, Feng Dou, Wang Wenqin, Liu Juan, Huang Ying, Gu Hang, Guo Dewei, Yao Ruojin, Ni Xin
Department of Gynecology and Obstetrics, Xiangya Hospital Central South University, Changsha 410008, China.
National International Joint Research Center for Medical Metabolomics, Xiangya Hospital Central South University, Changsha 410008, China.
Antioxidants (Basel). 2022 Jul 31;11(8):1505. doi: 10.3390/antiox11081505.
We have previously demonstrated that placental 11β-hydroxysteroid dehydrogenase type 2 (11β-HSD2) dysfunction contributes to PE pathogenesis. We sought to elucidate molecular mechanisms underlying 11β-HSD2 dysfunction-induced PE and to seek potential therapeutic targets using a 11β-HSD2 dysfunction-induced PE-like rat model as well as cultured extravillous trophoblasts (EVTs) since PE begins with impaired function of EVTs. In 11β-HSD2 dysfunction-induced PE-like rat model, we revealed that placental mitochondrial dysfunction occurred, which was associated with mitDNA instability and impaired mitochondrial dynamics, such as decreased optic atrophy 1 (OPA1) expression. MitoTEMPO treatment significantly alleviated the hallmark of PE-like features and improved mitDNA stability and mitochondrial dynamics in the placentas of rat PE-like model. In cultured human EVTs, we found that 11β-HSD2 dysfunction led to mitochondrial dysfunction and disrupted mtDNA stability. MitoTEMPO treatment improved impaired invasion and migration induced by 11β-HSD2 dysfunction in cultured EVTs. Further, we revealed that OPA1 was one of the key factors that mediated 11β-HSD2 dysfunction-induced excess ROS production, mitochondrial dysfunction and mtDNA reduction. Our data indicates that 11β-HSD2 dysfunction causes mitochondrial dysfunctions, which impairs trophoblast function and subsequently results in PE development. Our study immediately highlights that excess ROS is a potential therapeutic target for PE.
我们之前已经证明,胎盘2型11β-羟基类固醇脱氢酶(11β-HSD2)功能障碍与子痫前期的发病机制有关。由于子痫前期始于绒毛外滋养层细胞(EVT)功能受损,我们试图阐明11β-HSD2功能障碍诱导子痫前期的分子机制,并使用11β-HSD2功能障碍诱导的子痫前期样大鼠模型以及培养的绒毛外滋养层细胞(EVT)寻找潜在的治疗靶点。在11β-HSD2功能障碍诱导的子痫前期样大鼠模型中,我们发现胎盘线粒体功能障碍发生,这与线粒体DNA(mitDNA)不稳定和线粒体动力学受损有关,如视神经萎缩蛋白1(OPA1)表达降低。MitoTEMPO治疗显著减轻了子痫前期样特征的标志,并改善了子痫前期样大鼠模型胎盘的mitDNA稳定性和线粒体动力学。在培养的人EVT中,我们发现11β-HSD2功能障碍导致线粒体功能障碍并破坏线粒体DNA稳定性。MitoTEMPO治疗改善了11β-HSD2功能障碍在培养的EVT中诱导的侵袭和迁移受损。此外,我们发现OPA1是介导11β-HSD2功能障碍诱导的过量活性氧(ROS)产生、线粒体功能障碍和线粒体DNA减少的关键因素之一。我们的数据表明,11β-HSD2功能障碍导致线粒体功能障碍,损害滋养层细胞功能,随后导致子痫前期的发展。我们的研究立即突出了过量ROS是子痫前期的一个潜在治疗靶点。