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着床期小鼠子宫内膜中钙结合蛋白D-9k信使核糖核酸的表达

Expression of calcium binding protein D-9k messenger RNA in the mouse uterine endometrium during implantation.

作者信息

Tatsumi K, Higuchi T, Fujiwara H, Nakayama T, Itoh K, Mori T, Fujii S, Fujita J

机构信息

Department of Gynecology and Obstetrics, Faculty of Medicine, Kyoto University, Japan.

出版信息

Mol Hum Reprod. 1999 Feb;5(2):153-61. doi: 10.1093/molehr/5.2.153.

Abstract

To investigate the molecular mechanisms of implantation, we constructed a cDNA library of mouse uteri enriched with pregnancy-induced genes by subtractive hybridization and polymerase chain reaction (PCR). One of the isolated clones was the cDNA for the calcium binding protein D-9k (Cabp9k), which is considered to regulate intracytoplasmic concentration and transport of free calcium ions. Northern blot and in-situ hybridization analyses demonstrated that the Cabp9k mRNA was expressed in the endometrial epithelia, both luminal and glandular, in the uterus at the time of implantation. On pregnancy day 5 it was detected in the luminal, but not in the glandular, epithelia. In the oophorectomized adult mice, progesterone enhanced Cabp9k mRNA expression in the uterus, whereas oestrogen did not. Consistent with this, a nucleotide change was identified in the first intron of mouse Cabp9k gene corresponding to the oestrogen responsive element in the rat Cabp9k gene. Transfer of embryos into the uterine cavity of pseudopregnant mice reduced the expression of Cabp9k mRNA in the glandular epithelium, suggesting that Cabp9k mRNA expression is also regulated by embryonal signal(s). These findings demonstrated that Cabp9k mRNA is expressed in the endometrial epithelia during the implantation period under the control of progesterone and the presence of embryo, and suggest that CaBP9k plays a role in implantation by regulating the local calcium concentrations.

摘要

为了研究着床的分子机制,我们通过消减杂交和聚合酶链反应(PCR)构建了富含妊娠诱导基因的小鼠子宫cDNA文库。分离得到的一个克隆是钙结合蛋白D-9k(Cabp9k)的cDNA,该蛋白被认为可调节游离钙离子的胞浆浓度和转运。Northern印迹和原位杂交分析表明,Cabp9k mRNA在着床时子宫的腔上皮和腺上皮中均有表达。在妊娠第5天,在腔上皮中检测到了Cabp9k mRNA,但在腺上皮中未检测到。在去卵巢的成年小鼠中,孕酮可增强子宫中Cabp9k mRNA的表达,而雌激素则不能。与此一致的是,在小鼠Cabp9k基因的第一个内含子中发现了一个核苷酸变化,该变化与大鼠Cabp9k基因中的雌激素反应元件相对应。将胚胎移植到假孕小鼠的子宫腔中可降低腺上皮中Cabp9k mRNA的表达,这表明Cabp9k mRNA的表达也受胚胎信号的调节。这些发现表明,Cabp9k mRNA在着床期在孕酮和胚胎存在的控制下于子宫内膜上皮中表达,并提示CaBP9k通过调节局部钙浓度在着床中发挥作用。

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