Gao Fei, Lei Wei, Diao Hong-Lu, Hu Shi-Jun, Luan Li-Ming, Yang Zeng-Ming
Key Laboratory of the Ministry of Education for Cell Biology and Tumor Cell Engineering, College of Life Science, Xiamen University, Xiamen, China.
Fertil Steril. 2007 Oct;88(4 Suppl):1256-65. doi: 10.1016/j.fertnstert.2007.02.054. Epub 2007 May 11.
To examine the spatiotemporal expression and regulation of prostaglandin transporter (PGT), 15-hydroxy-PG dehydrogenase (15-PGDH), and carbonyl reductase 1 (CBR1) messenger RNA (mRNA) and protein in the mouse uterus during embryo implantation and in related models.
Experimental animal study.
University research laboratory.
ANIMAL(S): Sexually mature female Kunming strain white mice.
INTERVENTION(S): Delayed and activated implantation, artificial decidualization, and subcutaneous injection of progesterone (P) and E(2) in ovariectomized mouse.
MAIN OUTCOME MEASURE(S): The expression of mRNA and protein were detected by in situ hybridization and immunohistochemistry in mouse uterus.
RESULT(S): Prostaglandin transporter mRNA and protein were expressed in the subluminal stroma at implantation site on day 5 of pregnancy and then in decidua but were not detected at the interimplantation sites and in preimplantation or pseudopregnant uterus. The presence of an active blastocyst was required for PGT expression at the implantation site. Both 15-PGDH and CBR1 mRNA were detected in glandular epithelium on day 4 of pregnancies. The expression of 15-PGDH and CBR1 mRNA was also detected in postimplantation embryos.
CONCLUSION(S): These data suggest that differentially expressed PGT and 15-PGDH may participate in PG signaling in mouse uterus during implantation and decidualization.
研究前列腺素转运体(PGT)、15-羟基前列腺素脱氢酶(15-PGDH)和羰基还原酶1(CBR1)信使核糖核酸(mRNA)及蛋白在小鼠胚胎植入期子宫及相关模型中的时空表达及调控。
实验动物研究。
大学研究实验室。
性成熟的雌性昆明品系小白鼠。
延迟着床与激活着床、人工蜕膜化,以及对去卵巢小鼠皮下注射孕酮(P)和雌二醇(E2)。
采用原位杂交和免疫组化法检测小鼠子宫中mRNA和蛋白的表达。
妊娠第5天,PGT mRNA和蛋白在着床部位的腔下基质中表达,随后在蜕膜中表达,但在非着床部位、着床前或假孕子宫中未检测到。着床部位PGT表达需要有活性囊胚的存在。妊娠第4天,在腺上皮中检测到15-PGDH和CBR1 mRNA。在着床后胚胎中也检测到15-PGDH和CBR1 mRNA的表达。
这些数据表明,差异表达的PGT和15-PGDH可能在小鼠胚胎植入和蜕膜化过程中参与子宫内的PG信号传导。