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在着床期小鼠子宫中血管生成素-3 的差异表达和调控。

Differential expression and regulation of angiopoietin-3 in mouse uterus during preimplantation period.

机构信息

College of Animal Science and Veterinary Medicine, Jilin University, Changchun, P R China.

出版信息

J Exp Zool B Mol Dev Evol. 2012 Jun;318(4):316-24. doi: 10.1002/jez.b.22449.

DOI:10.1002/jez.b.22449
PMID:22821867
Abstract

Angiogenesis is necessary for successful implantation and decidualization. This study was to investigate the differential expression of angiopoietin-3 (Ang-3) in mouse uterus during early pregnancy and its regulation by steroid hormones using in situ hybridization and reverse transcription polymerase chain reaction (RT-PCR). There was no detectable Ang-3 mRNA signal on days 1-5 of pregnancy by in situ hybridization. On day 6 of pregnancy, a low level of Ang-3 mRNA signal was seen in the primary decidua. Ang-3 mRNA expression gradually increased on days 7 and 8 of pregnancy along with the development of decidua, and its expression scope was also expanded. The RT-PCR result indicated that Ang-3 mRNA expression was low on days 1-4 of pregnancy. On day 5, as embryo implanted, Ang-3 mRNA was highly expressed in mouse uterus, and the expression gradually increased on days 6-8 of pregnancy, with peak level on day 8 of pregnancy. Similarly, Ang-3 mRNA was also strongly expressed in decidualized cells under artificial decidualization. Compared with the delayed uterus, a high level of Ang-3 mRNA expression was detected in activated implantation uterus by RT-PCR. In the ovariectomized mouse uterus, Ang-3 mRNA expression increased and reached the highest level at 12 hr after injection of estrogen, progesterone, and estrogen plus progesterone, respectively. These results suggest that Ang-3 may play an important role during the process of mouse decidualization. Both estrogen and progesterone can induce the expression of Ang-3 in ovariectomized mouse uterus.

摘要

血管生成对于成功着床和蜕膜化是必要的。本研究旨在通过原位杂交和反转录聚合酶链反应(RT-PCR)技术,研究血管生成素-3(Ang-3)在小鼠子宫早期妊娠中的差异表达及其受类固醇激素的调控。通过原位杂交,在妊娠第 1-5 天未检测到 Ang-3 mRNA 信号。在妊娠第 6 天,初级蜕膜中可见低水平的 Ang-3 mRNA 信号。随着蜕膜的发育,Ang-3 mRNA 表达在妊娠第 7 天和第 8 天逐渐增加,其表达范围也扩大。RT-PCR 结果表明,妊娠第 1-4 天 Ang-3 mRNA 表达水平较低。第 5 天,胚胎着床时,小鼠子宫中 Ang-3 mRNA 表达水平较高,且在妊娠第 6-8 天逐渐增加,妊娠第 8 天达到高峰。同样,在人工蜕膜化的蜕膜化细胞中,Ang-3 mRNA 也强烈表达。与延迟子宫相比,通过 RT-PCR 检测到激活的着床子宫中 Ang-3 mRNA 表达水平较高。在卵巢切除小鼠的子宫中,Ang-3 mRNA 的表达增加,在分别注射雌激素、孕酮和雌激素加孕酮 12 小时后达到最高水平。这些结果表明,Ang-3 在小鼠蜕膜化过程中可能发挥重要作用。雌激素和孕酮均可诱导卵巢切除小鼠子宫中 Ang-3 的表达。

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