Bany B M, Harvey M B, Schultz G A
Department of Biochemistry and Molecular Biology, University of Calgary, Calgary, Alberta, Canada T2N 4N1.
J Reprod Fertil. 2000 Sep;120(1):125-34. doi: 10.1530/jrf.0.1200125.
During implantation, matrix metalloproteinases are believed to play roles in the tissue remodelling that accompanies decidualization in the endometrium and in embryo invasion. The objective of this study was to characterize further the expression of matrix metalloproteinases 2 and 9 in the mouse uterus during early pregnancy and oil-induced decidualization. mRNA encoding matrix metalloproteinase 2 was detected in pregnant uteri and uteri undergoing oil-induced decidualization by northern blot analyses. The steady-state concentrations of mRNA encoding matrix metalloproteinase 2 did not change significantly in implantation compared with inter-implantation areas on days 5-8 of pregnancy but were significantly lower in stimulated compared with non-stimulated uterine horns during artificially induced decidualization. mRNA encoding matrix metalloproteinase 9 was also detected in uteri undergoing oil-induced decidualization but not in pregnant uteri. Its concentration was significantly greater in uterine horns undergoing oil-induced decidualization compared with control horns. Immunoreactive matrix metalloproteinases 2 and 9 were detected in the uterus during early pregnancy and oil-induced decidualization by immunohistochemistry, localized to the endometrial stroma, but the staining progressively became weaker and was absent in areas that had undergone decidualization. By day 8 of pregnancy and 72 h after the induction of decidualization, matrix metalloproteinase 2 and 9 proteins remained mainly in the region of non-decidualized stromal cells adjacent to the myometrium. In implantation segments, they were also localized to the region of the trophoblast giant cells. The second objective of the present study was to determine whether endometrial stromal cells isolated from uteri sensitized for decidualization express matrix metalloproteinases 2 and 9. Northern blot analyses and gelatin zymography showed that these cultured cells expressed matrix metalloproteinase 2 and 9, and that transforming growth factor beta1 significantly increased matrix metalloproteinase 9 expression. The results of the present study further characterize matrix metalloproteinases 2 and 9 expression in the uterus during implantation and artificially induced decidualization.
在植入过程中,基质金属蛋白酶被认为在子宫内膜蜕膜化及胚胎侵入所伴随的组织重塑中发挥作用。本研究的目的是进一步表征妊娠早期和油诱导蜕膜化过程中小鼠子宫中基质金属蛋白酶2和9的表达情况。通过Northern印迹分析在妊娠子宫和经历油诱导蜕膜化的子宫中检测到了编码基质金属蛋白酶2的mRNA。在妊娠第5 - 8天,与非植入区域相比,植入部位编码基质金属蛋白酶2的mRNA稳态浓度没有显著变化,但在人工诱导蜕膜化过程中,与未刺激的子宫角相比,刺激后的子宫角中该mRNA浓度显著降低。在经历油诱导蜕膜化的子宫中也检测到了编码基质金属蛋白酶9的mRNA,但在妊娠子宫中未检测到。与对照子宫角相比,经历油诱导蜕膜化的子宫角中其浓度显著更高。通过免疫组织化学在妊娠早期和油诱导蜕膜化过程中的子宫中检测到了免疫反应性基质金属蛋白酶2和9,定位于子宫内膜基质,但染色逐渐变弱,在已经发生蜕膜化的区域消失。到妊娠第8天和诱导蜕膜化72小时后,基质金属蛋白酶2和9蛋白主要仍存在于与子宫肌层相邻的未蜕膜化基质细胞区域。在植入节段中,它们也定位于滋养层巨细胞区域。本研究的第二个目的是确定从对蜕膜化敏感的子宫中分离的子宫内膜基质细胞是否表达基质金属蛋白酶2和9。Northern印迹分析和明胶酶谱分析表明,这些培养细胞表达基质金属蛋白酶2和9,并且转化生长因子β1显著增加基质金属蛋白酶9的表达。本研究结果进一步表征了植入和人工诱导蜕膜化过程中子宫中基质金属蛋白酶2和9的表达情况。