Obstetrics and Gynecology Hospital, Fudan University, Shanghai, PR China; Shanghai Key Laboratory of Female Reproductive Endocrine Related Diseases, Shanghai, PR China.
Placenta. 2013 Nov;34(11):1044-52. doi: 10.1016/j.placenta.2013.07.070. Epub 2013 Sep 17.
The expression of human leucocyte antigen-G (HLA-G) in trophoblasts plays a crucial role in successful embryonic implantation, and reduced HLA-G expression might contribute to adverse obstetric outcomes. In this study, we silenced HLA-G expression using RNA interference in JEG-3 cells, resulting in a notably attenuated invasion capacity of the cells in a Transwell assay; however, no alterations in cell proliferation or apoptosis were observed. The down-regulation of HLA-G dampened the activation of signal transducer and activator of transcription 3 (STAT3), whereas the up-regulation of HLA-G promoted STAT3 activation and invasion in JEG-3 cells treated with human galectin-1. Most importantly, interleukin-6 (IL-6), but not galectin-1, was shown to rescue invasion deficiency in a dose-dependent manner. Thus, we demonstrate that HLA-G is able to regulate JEG-3 cell invasion by influencing STAT3 activation, which may underlie the implantation defects accompanying HLA-G hypo-expression in pre-eclampsia.
人类白细胞抗原-G(HLA-G)在滋养细胞中的表达对于成功的胚胎着床起着至关重要的作用,而 HLA-G 表达的减少可能导致不良的产科结局。在这项研究中,我们使用 RNA 干扰沉默了 JEG-3 细胞中的 HLA-G 表达,结果在 Transwell 分析中明显减弱了细胞的侵袭能力;然而,细胞增殖或凋亡没有观察到变化。HLA-G 的下调抑制了信号转导和转录激活因子 3(STAT3)的激活,而 JEG-3 细胞中 HLA-G 的上调促进了 STAT3 的激活和侵袭,这些细胞用人类半乳糖凝集素-1 处理。最重要的是,白细胞介素-6(IL-6)而不是半乳糖凝集素-1,能够以剂量依赖的方式挽救侵袭缺陷。因此,我们证明 HLA-G 能够通过影响 STAT3 的激活来调节 JEG-3 细胞的侵袭,这可能是子痫前期中 HLA-G 低表达导致着床缺陷的基础。