Chen Yao-Yu, Chuang Pei-Yun, Chen Chie-Pein, Chiu Yueh-Ho, Lo Hsiao-Fan, Cheong Mei-Leng, Huang Jyun-Yuang, Kuo Pao-Lin, Chen Hungwen
Graduate Institute of Biochemical Sciences, National Taiwan University, Taipei 106, Taiwan.
Division of High Risk Pregnancy, Mackay Memorial Hospital, Taipei 104, Taiwan.
J Biol Chem. 2014 Aug 15;289(33):22958-22968. doi: 10.1074/jbc.M114.576744. Epub 2014 Jul 7.
Human trophoblast invasion of decidualized endometrium is essential for placentation and is tightly regulated and involves trophoblast-decidual cell interaction. High temperature requirement A4 (HtrA4) is a secreted serine protease highly expressed in the invasive extravillous trophoblasts that invade decidua. In contrast, both HtrA1 and HtrA3 have been shown to inhibit trophoblast invasion. Here we provide evidence that decidua-secreted HtrA1 and HtrA3 antagonize HtrA4-mediated trophoblast invasion. We demonstrated that HtrA1 and HtrA3 interact with and degrade HtrA4 and thereby inhibit trophoblast-like JAR cell invasion. Specifically, HtrA1 and HtrA3 expression is up-regulated under decidualization conditions in endometrial stromal and epithelial cells, T-HESCs and Ishikawa cells, respectively. Conditioned media from these two cell lines after decidualization treatment suppress HtrA4-expressing JAR cell invasion in an HtrA1- or HtrA3-dependent manner. Co-culture of the HtrA4-expressing JAR cells with decidualization stimuli-treated T-HESC or Ishikawa monolayer also impairs JAR cell invasion, which can be reversed by HtrA1 or HtrA3 knockdown, supporting that HtrA1 and HtrA3 are crucial for trophoblast-decidual cell interaction in the control of trophoblast invasion. Our study reveals a novel regulatory mechanism of trophoblast invasion through physical and functional interaction between HtrA family members.
人滋养层细胞侵入蜕膜化的子宫内膜对于胎盘形成至关重要,且受到严格调控,涉及滋养层细胞与蜕膜细胞的相互作用。高温需求蛋白A4(HtrA4)是一种分泌型丝氨酸蛋白酶,在侵入蜕膜的侵袭性绒毛外滋养层细胞中高度表达。相比之下,HtrA1和HtrA3均已被证明可抑制滋养层细胞的侵袭。在此,我们提供证据表明,蜕膜分泌的HtrA1和HtrA3可拮抗HtrA4介导的滋养层细胞侵袭。我们证明,HtrA1和HtrA3与HtrA4相互作用并使其降解,从而抑制滋养层样JAR细胞的侵袭。具体而言,在蜕膜化条件下,HtrA1和HtrA3的表达分别在子宫内膜基质细胞和上皮细胞、T-HESC细胞和石川细胞中上调。蜕膜化处理后的这两种细胞系的条件培养基以HtrA1或HtrA3依赖的方式抑制表达HtrA4的JAR细胞的侵袭。将表达HtrA4的JAR细胞与经蜕膜化刺激处理的T-HESC细胞或石川细胞单层共培养也会损害JAR细胞的侵袭,而HtrA1或HtrA3基因敲低可逆转这种损害,这支持了HtrA1和HtrA3在控制滋养层细胞侵袭的滋养层细胞与蜕膜细胞相互作用中起关键作用。我们的研究揭示了一种通过HtrA家族成员之间的物理和功能相互作用来调控滋养层细胞侵袭的新机制。