Cong Jing, Diao Hong-Lu, Zhao Yue-Chao, Ni Hua, Yan Yun-Qin, Yang Zeng-Ming
College of Life Sciences, Northeast Agricultural University, Harbin 150030, People's Republic of China.
Reproduction. 2006 Jan;131(1):139-51. doi: 10.1530/rep.1.00861.
It has been shown that both prostaglandin I2 (PGI2) and PGE2 are essential for mouse implantation, whereas only PGE2 is required for hamster implantation. To date, the expression and regulation of cyclooxygenase (COX) and prostaglandin E synthase (PGES), which are responsible for PGE2 production, have not been reported in the rat. The aim of this study was to examine the expression pattern and regulation of COX-1, COX-2, membrane-associated PGES-1 (mPGES-1), mPGES-2 and cytosolic PGES (cPGES) in rat uterus during early pregnancy and pseudopregnancy, and under delayed implantation. At implantation site on day 6 of pregnancy, COX-1 immunostaining was highly visible in the luminal epithelium, and COX-2 immunostaining was clearly observed in the subluminal stroma. Both mPGES-1 mRNA and protein were only observed in the subluminal stroma surrounding the implanting blastocyst at the implantation site on day 6 of pregancy , but were not seen in the inter-implantation site on day 6 of pregnancy and on day 6 of pseudopregnancy. Our data suggest that the presence of an active blastocyst is required for mPGES-1 expression at the implantation site. When pregnant rats on day 5 were treated with nimesulide for 24 h, mPGES-1 protein expression was completely inhibited. cPGES immunostaining was clearly observed in the luminal epithelium and subluminal stromal cells immediately surrounding the implanting blastocyst on day 6 of pregnancy. mPGES-2 immunostaining was clearly seen in the luminal epithelium at the implantation site. Additionally, immunostaining for prostaglandin I synthase (PGIS) was also strongly detected at the implantation site. In conclusion, our results indicate that PGE2 and PGI2 should have a very important role in rat implantation.
研究表明,前列腺素I2(PGI2)和前列腺素E2(PGE2)对小鼠着床均至关重要,而仓鼠着床仅需PGE2。迄今为止,尚未见有关负责PGE2生成的环氧化酶(COX)和前列腺素E合酶(PGES)在大鼠中的表达及调控的报道。本研究旨在检测妊娠早期、假孕及延迟着床状态下大鼠子宫中COX-1、COX-2、膜相关PGES-1(mPGES-1)、mPGES-2和胞质PGES(cPGES)的表达模式及调控情况。在妊娠第6天的着床部位,COX-1免疫染色在腔上皮中高度可见,COX-2免疫染色在腔下基质中清晰可见。mPGES-1 mRNA和蛋白仅在妊娠第6天着床部位围绕着床胚泡的腔下基质中观察到,而在妊娠第6天的非着床部位及假孕第6天未见。我们的数据表明,着床部位mPGES-1的表达需要活性胚泡的存在。妊娠第5天的大鼠用尼美舒利处理24小时后,mPGES-1蛋白表达被完全抑制。妊娠第6天,cPGES免疫染色在紧邻着床胚泡的腔上皮和腔下基质细胞中清晰可见。mPGES-2免疫染色在着床部位的腔上皮中清晰可见。此外,在着床部位也强烈检测到前列腺素I合酶(PGIS)的免疫染色。总之,我们的结果表明PGE2和PGI2在大鼠着床中应具有非常重要的作用。