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在着床期间,孕酮刺激子宫中降钙素基因的表达。

Progesterone stimulates calcitonin gene expression in the uterus during implantation.

作者信息

Ding Y Q, Zhu L J, Bagchi M K, Bagchi I C

机构信息

Population Council, New York, New York 10021.

出版信息

Endocrinology. 1994 Nov;135(5):2265-74. doi: 10.1210/endo.135.5.7956949.

Abstract

Implantation of the mammalian embryo into the wall of the uterus is regulated by a timely interplay of the ovarian hormones, estrogen and progesterone. These hormones orchestrate a set of modifications in the uterine endometrium that transforms it from a nonreceptive to a receptive phase allowing the implantation of the developing blastocyst. The molecular and cellular mechanisms underlying this complex process, however, remain largely unknown. To investigate the endocrine basis of uterine receptivity, we employed a gene expression screen technique to identify factors whose expressions are modulated in the rat uterus in response to estrogen and progesterone at the onset of implantation. Here we report that the expression of calcitonin, a peptide hormone involved in calcium homeostasis, is markedly enhanced in the uterus during pregnancy. By Northern blot analysis, we show that the synthesis of calcitonin messenger RNA is induced at the time of implantation. Immunocytochemistry with calcitonin antibody demonstrates further that the peptide is localized in the glandular epithelial cells of the uterus. The antiprogestin drug RU486, which is known to block implantation, abolishes calcitonin expression, suggesting a regulatory role for progesterone in this process. Consistent with this observation, progesterone significantly stimulates calcitonin messenger RNA and protein synthesis in the uteri of ovariectomized animals. Our study, therefore, identifies calcitonin as a stage- and cell-specific marker of progesterone action in the uterus during pregnancy. Estrogen exhibits no significant effect on calcitonin expression when administered alone to ovariectomized animals. However, a low dose of estrogen synergizes with progesterone, and a high dose antagonizes progesterone-mediated gene induction. Both estrogen and progesterone, therefore, modulate calcitonin gene expression in the uterus. The stage-specific regulation of calcitonin is apparently determined by the relative concentrations and the sequences of appearance of these two hormones and possibly other as yet unknown regulatory factors during pregnancy. We propose that calcitonin, a known regulator of calcium levels in the bone and kidney, may play an important regulatory role in the uterus of pregnant animals during the early events leading to implantation of the embryo.

摘要

哺乳动物胚胎植入子宫壁是由卵巢激素雌激素和孕酮适时相互作用来调节的。这些激素协调子宫内膜发生一系列变化,使其从非接受期转变为接受期,从而允许发育中的囊胚植入。然而,这一复杂过程背后的分子和细胞机制在很大程度上仍不清楚。为了研究子宫接受性的内分泌基础,我们采用基因表达筛选技术来鉴定在植入开始时,大鼠子宫中其表达受雌激素和孕酮调节的因子。在此我们报告,降钙素(一种参与钙稳态的肽类激素)在妊娠期间子宫中的表达显著增强。通过Northern印迹分析,我们表明在植入时诱导了降钙素信使核糖核酸的合成。用降钙素抗体进行免疫细胞化学进一步证明该肽定位于子宫的腺上皮细胞中。已知能阻断植入的抗孕激素药物RU486消除了降钙素的表达,提示孕酮在此过程中起调节作用。与这一观察结果一致,孕酮显著刺激去卵巢动物子宫中降钙素信使核糖核酸和蛋白质的合成。因此,我们的研究确定降钙素是妊娠期间子宫中孕酮作用的阶段和细胞特异性标志物。单独给去卵巢动物施用雌激素时,对降钙素表达没有显著影响。然而,低剂量雌激素与孕酮协同作用,高剂量则拮抗孕酮介导的基因诱导。因此,雌激素和孕酮都调节子宫中降钙素基因的表达。降钙素的阶段特异性调节显然是由这两种激素在妊娠期间的相对浓度和出现顺序以及可能其他尚未知的调节因子决定的。我们提出,降钙素作为骨和肾中已知的钙水平调节因子,可能在妊娠动物子宫中导致胚胎植入的早期事件中发挥重要调节作用。

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