Fujito Naoya, Samura Osamu, Miharu Norio, Tanigawa Miho, Hyodo Maki, Kudo Yoshiki
Department of Obstetrics and Gynecology, Graduate School of Biomedical Sciences, Hiroshima University, Hiroshima, Japan.
Hiroshima J Med Sci. 2006 Mar;55(1):9-15.
In this study we have investigated whether quantitative analysis of placental mRNAs in maternal plasma provides a way to monitor placental status. We measured plasma concentrations of human chorionic gonadotropin beta-subunit (betahCG) and human placental lactogen (hPL) mRNAs as previously reported mRNAs and pregnancy associated plasma protein A (PAPP-A), placenta-specific 1 (PLAC1) and glial cells-missing 1 (GCM1) mRNAs, which have not been measured during the course of normal pregnancy. Firstly, peripheral blood was obtained at various times from healthy pregnant women to clarify the time course of placental mRNAs. Secondly, blood was obtained from women with pre-eclampsia and gestational age-matched controls to examine whether placental mRNAs change in pre-eclampsia. Plasma was separated from these samples for extraction of RNA, followed by reverse transcription polymerse chain reaction analysis. Median concentrations of PLAC1 and GCM1 mRNA in plasma of pre-eclamptic subjects respectively were 1625 and 2141 copies/ml, significantly higher than 195 and 881 copies/ml, the values for controls (Mann-Whitney test, p<0.001). No significant difference was seen in hPL, betahCG, or PAPP-A mRNA concentration between pre-eclamptic and control groups. Plasma PLAC1 and GCM1 mRNAs appear promising as noninvasively measurable molecular markers for pre-eclampsia.
在本研究中,我们调查了母体血浆中胎盘mRNA的定量分析是否能提供一种监测胎盘状态的方法。我们测量了血浆中人绒毛膜促性腺激素β亚基(βhCG)和人胎盘催乳素(hPL)的mRNA浓度,这两种mRNA是此前已报道过的,同时还测量了妊娠相关血浆蛋白A(PAPP-A)、胎盘特异性1(PLAC1)和神经胶质细胞缺失1(GCM1)的mRNA浓度,在正常妊娠过程中尚未对这些mRNA进行过测量。首先,在不同时间从健康孕妇获取外周血,以明确胎盘mRNA的时间进程。其次,从患有先兆子痫的女性及其孕周匹配的对照组获取血液,以检查先兆子痫时胎盘mRNA是否发生变化。从这些样本中分离出血浆用于RNA提取,随后进行逆转录聚合酶链反应分析。先兆子痫患者血浆中PLAC1和GCM1 mRNA的中位数浓度分别为1625和2141拷贝/毫升,显著高于对照组的195和881拷贝/毫升(Mann-Whitney检验,p<0.001)。先兆子痫组和对照组之间hPL、βhCG或PAPP-A mRNA浓度未见显著差异。血浆PLAC1和GCM1 mRNA有望成为先兆子痫的无创可测分子标志物。