Godbole Geeta, Suman Pankaj, Malik Ankita, Galvankar Mosami, Joshi Niraj, Fazleabas Asgerally, Gupta Satish Kumar, Modi Deepak
Molecular and Cellular Biology Laboratory, National Institute for Research in Reproductive Health, Indian Council of Medical Research, Parel, Mumbai 400012, India.
Reproductive Cell Biology Laboratory, National Institute of Immunology, New Delhi 110067, India.
Endocrinology. 2017 Aug 1;158(8):2618-2633. doi: 10.1210/en.2017-00032.
An important step toward successful pregnancy involves invasion of the trophoblast cells into the decidua for placentation. Herein, we show that in the human and baboon decidua HOXA10 expression is downregulated after implantation and that this reduction is most prominent in the decidual cells juxtaposed to the invading placental villi. The supernatants derived from HOXA10-depleted human decidual cells increase the invasiveness of the trophoblast cell lines ACH-3P and JEG3 in vitro; this increase is due to higher expression and activity of matrix metalloproteases (MMPs) and reduced expression of tissue inhibitors of MMPs in both the cell lines. The proinvasive ability of HOXA10-depleted decidual cells is due to increased levels and secretion of leukemia inhibitor factor (LIF) and interleukin (IL)-6. Both these cytokines individually promote invasion of ACH-3P and JEG3 cell by increasing the activities of MMPs and decreasing mRNA levels of TIMPs. Finally, we demonstrate that the supernatants derived from HOXA10-depleted decidual cell-phosphorylated STAT3 (Tyr 705) and knocking down STAT3 in ACH-3P and JEG3 cells restrained the invasion mediated by supernatants derived from HOXA10-depleted decidual cells. These results imply that STAT3 activity is essential and sufficient to promote invasion in response to downregulation of HOXA10 in decidual cells. We propose that downregulation of HOXA10 in the decidual cells promotes the expression of LIF and IL-6, which, in a paracrine manner, activates STAT3 in the trophoblast cells, leading to an increase in MMPs to facilitate invasion.
成功怀孕的一个重要步骤是滋养层细胞侵入蜕膜以进行胎盘形成。在此,我们表明,在人类和狒狒的蜕膜中,HOXA10的表达在着床后下调,并且这种降低在与侵入的胎盘绒毛相邻的蜕膜细胞中最为明显。源自HOXA10缺失的人蜕膜细胞的上清液在体外增加了滋养层细胞系ACH-3P和JEG3的侵袭性;这种增加是由于两种细胞系中基质金属蛋白酶(MMPs)的表达和活性更高,以及MMP组织抑制剂的表达降低。HOXA10缺失的蜕膜细胞的促侵袭能力归因于白血病抑制因子(LIF)和白细胞介素(IL)-6水平和分泌的增加。这两种细胞因子各自通过增加MMPs的活性和降低TIMPs的mRNA水平来促进ACH-3P和JEG3细胞的侵袭。最后,我们证明,源自HOXA10缺失的蜕膜细胞的上清液使STAT3(Tyr 705)磷酸化,并且在ACH-3P和JEG3细胞中敲低STAT3可抑制源自HOXA10缺失的蜕膜细胞的上清液介导的侵袭。这些结果表明,STAT3活性对于响应蜕膜细胞中HOXA10的下调促进侵袭是必不可少且足够的。我们提出,蜕膜细胞中HOXA10的下调促进了LIF和IL-6的表达,它们以旁分泌方式激活滋养层细胞中的STAT3,导致MMPs增加以促进侵袭。