...
首页> 外文期刊>Journal of reproduction and fertility >Temporal- and hormone-dependent changes in uterine sensitization for the decidual cell reaction and decidualization in vitro of rat endometrial stromal cells
【24h】

Temporal- and hormone-dependent changes in uterine sensitization for the decidual cell reaction and decidualization in vitro of rat endometrial stromal cells

机译:子宫内膜基质细胞蜕膜细胞反应和体外蜕膜的子宫敏感性的时间和激素依赖性变化

获取原文

摘要

The ability of endometrial stromal cells from nonsensitized rat uteri to undergo decidualization in vitro was investigated. Cells were obtained by enzymatic dispersion from uteri of ovariectomized, steroid-treated rats at the equivalent of day 4, 5 or 6 of pseudopregnancy, or on day 5 from rats treated with 0, 0.3 or 1.0 μg oestradiol (low, intermediate or high doses of oestradiol, respectively) on day 4, and cultured for 24, 48 or 72 h. Decidualization in vivo, as assessed by uterine mass 5 days after the unilateral intrauterine injection of 100 μl sesame oil, was maximal for rats receiving the deciduogenic stimulus on day 5 and treated with the intermediate dose of oestradiol. Under control conditions in vitro, alkaline phosphatase (ALP) activity, the increase in ALP activity with time, and prostaglandin E2 (PGE2) accumulation in the medium were greatest for cells from maximally sensitized uteri. Indomethacin, an inhibitor of PG synthesis, reduced PGE2 accumulation to barely detectable amounts, and decreased ALP activity, especially in cells from maximally sensitized uteri, indicating that endogenous PG production contributed to the increase in ALP activity in these cells. The addition of PGE2 with indomethacin increased ALP activities. However, ALP activities were lower for cells derived from nonsensitized uteri when compared with cells from maximally sensitized uteri. These results suggest that endometrial stromal cells from nonsensitized uteri have a reduced capacity to undergo decidualization in vitro, and that this reduced capacity is not explained by differences in PGE2 production.
机译:研究了来自非致敏大鼠子宫的子宫内膜间质细胞体外蜕膜化的能力。通过酶促分散从卵巢切除,经类固醇治疗的大鼠子宫中获得的细胞,相当于假孕的第4、5或6天,或在第5天从接受0、0.3或1.0μg雌二醇(低,中或高剂量)治疗的大鼠中获得在第4天,分别进行一次雌二醇培养,并培养24、48或72小时。单侧宫腔内注射100μl芝麻油5天后通过子宫肿块评估,在体内的蜕膜形成对于第5天接受了十聚体刺激并用中等剂量的雌二醇治疗的大鼠最大。在体外控制条件下,碱性磷酸酶(ALP)活性,ALP活性随时间的增加以及培养基中前列腺素E2(PGE2)的积累对于最大敏化子宫的细胞最大。吲哚美辛是PG合成的抑制剂,特别是在来自最大致敏子宫的细胞中,将PGE2的积累减少到几乎无法检测到的水平,并且ALP活性降低,表明内源性PG的产生有助于这些细胞中ALP活性的增加。与吲哚美辛一起添加PGE2可提高ALP活性。然而,与最大敏感性子宫细胞相比,非敏感性子宫细胞的ALP活性较低。这些结果表明,来自非致敏子宫的子宫内膜基质细胞的体外蜕膜化能力降低,并且这种降低的能力不能通过PGE2产生的差异来解释。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号