Wong Becky S Y, Liu Shiying, Schultz Gilbert A, Rancourt Derrick E
Department of Biochemistry and Molecular Biology, University of Calgary Health Sciences Centre, Calgary, Canada.
Mol Reprod Dev. 2002 Apr;61(4):453-9. doi: 10.1002/mrd.10113.
During implantation, a balance of factors regulates the invasive properties of the embryo and the anti-invasive properties of uterine decidua. Although antiproteinases such as the metalloproteinase inhibitor TIMP-3 are thought to play critical roles in preventing the overaggressive invasion of trophoblasts, the mechanism of antiproteinase regulation is unknown. Recently, the prohormone convertase SPC-6 has been found to be co-expressed in embryo-proximal decidua in association with TIMP-3. As members of this serine proteinase family are known to activate latent TGFbeta family members which regulate decidual TIMP-3 levels, we sought to characterize the expression of SPC-6 during pregnancy and artificial decidualization. In this study, we demonstrate that the zone of SPC-6 gene expression exhibits a great degree of temporal and spatial overlap with TIMP-3 gene expression in uterine decidua from E5.5 through to E8.5. Like TIMP-3, we demonstrate that SPC-6 expression is induced during the decidual cell response using an in vivo model of artificial decidualization. Both the secreted and membrane bound forms of SPC-6 are expressed throughout the period of decidualization, suggesting that SPC-6 may play multiple roles during this developmental period. This is confirmed by our observation of the movement of SPC-6 expression to the presumptive placental region, as TIMP-3 expression regresses at the implantation site.
在植入过程中,多种因素相互平衡,调节胚胎的侵入特性和子宫蜕膜的抗侵入特性。尽管诸如金属蛋白酶抑制剂TIMP-3等抗蛋白酶被认为在防止滋养层过度侵袭中起关键作用,但其调节机制尚不清楚。最近,发现激素原转化酶SPC-6与TIMP-3共同在胚胎近端蜕膜中表达。由于已知该丝氨酸蛋白酶家族的成员可激活调节蜕膜TIMP-3水平的潜伏TGFβ家族成员,我们试图表征妊娠和人工蜕膜化过程中SPC-6的表达情况。在本研究中,我们证明从E5.5到E8.5,子宫蜕膜中SPC-6基因表达区域与TIMP-3基因表达在时间和空间上有很大程度的重叠。与TIMP-3一样,我们利用人工蜕膜化的体内模型证明,SPC-6表达在蜕膜细胞反应过程中被诱导。在整个蜕膜化期间,SPC-6的分泌形式和膜结合形式均有表达,这表明SPC-6在这一发育阶段可能发挥多种作用。随着TIMP-3表达在植入部位消退,SPC-6表达向推定胎盘区域移动,这一观察结果证实了上述结论。