Yasui Y, Yamaguchi M, Jikihara H, Yamamoto T, Kanzaki T, Murata Y
Department of Specific Organ Regulation, Osaka University Graduate School of Medicine, Suita, Japan.
Endocr J. 2001 Jun;48(3):397-401. doi: 10.1507/endocrj.48.397.
The aims of this study were to determine whether the human placenta and decidua express PRL-releasing peptide (PrRP) mRNA and whether PrRP regulates PRL secretion from cultured human decidual cells. PrRP gene expression was analyzed by reverse transcription (RT)-PCR, and the level of the gene expression was quantified by a ribonuclease protection assay. PrRP gene expression was detected in both the placenta and decidua. These tissues expressed PrRP mRNA throughout pregnancy and the level of PrRP mRNA expression somewhat increased during midpregnancy. Placental and decidual cells also expressed PrRP mRNA, in vitro. To determine whether PrRP affects decidual PRL secretion, human endometrial stromal cells and decidual cells were cultured and treated with or without 1 microM PrRP31. PrRP31 did not affect PRL secretion in either short or long term incubation. Moreover, the RT-PCR analysis indicated that human decidua does not express the PrRP receptor, hGR3, mRNA. These findings suggest that PrRP produced by the human placenta and decidua does not affect decidual PRL secretion due to a lack of the receptor, and that it may play other roles during pregnancy.
本研究的目的是确定人胎盘和蜕膜是否表达催乳素释放肽(PrRP)mRNA,以及PrRP是否调节培养的人蜕膜细胞的催乳素分泌。通过逆转录(RT)-PCR分析PrRP基因表达,并通过核糖核酸酶保护试验定量基因表达水平。在胎盘和蜕膜中均检测到PrRP基因表达。这些组织在整个孕期均表达PrRP mRNA,且PrRP mRNA表达水平在妊娠中期有所增加。胎盘细胞和蜕膜细胞在体外也表达PrRP mRNA。为了确定PrRP是否影响蜕膜催乳素分泌,培养人子宫内膜基质细胞和蜕膜细胞,并分别用1 microM PrRP31处理或不处理。PrRP31在短期或长期孵育中均不影响催乳素分泌。此外,RT-PCR分析表明,人蜕膜不表达PrRP受体hGR3 mRNA。这些发现表明,由于缺乏受体,人胎盘和蜕膜产生的PrRP不影响蜕膜催乳素分泌,并且它可能在孕期发挥其他作用。