基质金属蛋白酶2和9在小鼠子宫着床和油诱导脱胎化过程中的表达。

B M Bany, M B Harvey, G A Schultz
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引用次数: 57

摘要

在着床过程中,基质金属蛋白酶被认为在子宫内膜脱个体化的组织重塑和胚胎侵袭中发挥作用。本研究的目的是进一步表征基质金属蛋白酶2和9在小鼠早期妊娠和油诱导脱胎化子宫中的表达。northern blot检测妊娠和油致去胎化子宫中基质金属蛋白酶2的mRNA编码。妊娠第5 ~ 8天着床部位编码基质金属蛋白酶2的mRNA稳态浓度与着床间区相比变化不显著,但在人工诱导脱胎化过程中,受刺激子宫角的mRNA稳态浓度显著低于未受刺激子宫角。在油诱导脱胎化的子宫中也检测到编码基质金属蛋白酶9的mRNA,但在妊娠子宫中未检测到。其浓度在油致脱个体化子宫角中显著高于对照子宫角。免疫组化在妊娠早期和油变性子宫中检测到免疫反应性基质金属蛋白酶2和9,定位于子宫内膜间质,但染色逐渐变弱,在发生脱变性的区域无染色。在妊娠第8天和脱个体诱导72 h后,基质金属蛋白酶2和9蛋白主要存在于肌层附近未脱个体的基质细胞区域。在植入节段,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子宫分离的子宫内膜间质细胞是否表达基质金属蛋白酶2和9。Northern blot和明胶酶谱分析显示,这些培养细胞表达基质金属蛋白酶2和9,转化生长因子β 1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基质金属蛋白酶2和9在子宫着床和人工诱导脱个体化过程中的表达。
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Expression of matrix metalloproteinases 2 and 9 in the mouse uterus during implantation and oil-induced decidualization.

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.

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