Pollheimer J, Husslein P, Knöfler M
Department of Obstetrics and Gynecology, Medical University of Vienna, Waehringer Guertel 18-20, A-1090 Vienna, Austria.
Placenta. 2005 Apr;26 Suppl A:S42-5. doi: 10.1016/j.placenta.2004.12.005.
Endostatin, the C-terminal proteolytic fragment of the noncollagenous domain 1 (NC1) of the basement membrane protein collagen XVIII, inhibits cell proliferation and migration. Placental and decidual expression of the peptide suggested a role in angiogenesis and/or extravillous trophoblast differentiation. Here, we demonstrate that supernatants of trophoblastic SGHPL-5 cells, purified first trimester villous trophoblasts and villous explant cultures contain proteases which in vitro cleave 20kDa endostatin from purified, recombinant NC1 domains. However, supernatants of decidual and villous fibroblasts failed to generate the 20kDa endostatin fragment. Moreover, we show that recombinant endostatin inhibits invasion of SGHPL-5 cells through Matrigel invasion chambers. Since mesenchymal cells but not trophoblasts produce collagen XVIII we suspect that invasive trophoblasts may produce endostatin upon contacting the extracellular matrix deposited by decidual stromal cells. Generation of endostatin through trophoblast-derived proteases could play a role in the regulation of trophoblast invasiveness.
内皮抑素是基底膜蛋白胶原蛋白 XVIII 的非胶原结构域 1(NC1)的 C 末端蛋白水解片段,可抑制细胞增殖和迁移。该肽在胎盘和蜕膜中的表达表明其在血管生成和/或绒毛外滋养层细胞分化中发挥作用。在此,我们证明滋养层 SGHPL-5 细胞、纯化的孕早期绒毛滋养层细胞和绒毛外植体培养物的上清液中含有蛋白酶,这些蛋白酶在体外可从纯化的重组 NC1 结构域切割出 20kDa 的内皮抑素。然而,蜕膜和成纤维细胞的上清液未能产生 20kDa 的内皮抑素片段。此外,我们表明重组内皮抑素可抑制 SGHPL-5 细胞通过基质胶侵袭小室的侵袭。由于间充质细胞而非滋养层细胞产生胶原蛋白 XVIII,我们推测侵袭性滋养层细胞在接触蜕膜基质细胞沉积的细胞外基质时可能产生内皮抑素。通过滋养层来源的蛋白酶生成内皮抑素可能在调节滋养层侵袭性中发挥作用。