Chim Stephen S C, Shing Tristan K F, Hung Emily C W, Leung Tak-Yeung, Lau Tze-Kin, Chiu Rossa W K, Lo Y M Dennis
Centre for Research into Circulating Fetal Nucleic Acids, Li Ka Shing Institute of Health Sciences, The Chinese University of Hong Kong, Prince of Wales Hospital, Shatin, Hong Kong SAR, China.
Clin Chem. 2008 Mar;54(3):482-90. doi: 10.1373/clinchem.2007.097972. Epub 2008 Jan 24.
The discovery of circulating fetal nucleic acids in maternal plasma has opened up new possibilities for noninvasive prenatal diagnosis. MicroRNAs (miRNAs), a class of small RNAs, have been intensely investigated recently because of their important regulatory role in gene expression. Because nucleic acids of placental origin are released into maternal plasma, we hypothesized that miRNAs produced by the placenta would also be released into maternal plasma.
We systematically searched for placental miRNAs in maternal plasma to identify miRNAs that were at high concentrations in placentas compared with maternal blood cells and then investigated the stability and filterability of this novel class of pregnancy-associated markers in maternal plasma.
In a panel of TaqMan MicroRNA Assays available for 157 well-established miRNAs, 17 occurred at concentrations >10-fold higher in the placentas than in maternal blood cells and were undetectable in postdelivery maternal plasma. The 4 most abundant of these placental miRNAs (miR-141, miR-149, miR-299-5p, and miR-135b) were detectable in maternal plasma during pregnancy and showed reduced detection rates in postdelivery plasma. The plasma concentration of miR-141 increased as pregnancy progressed into the third trimester. Compared with mRNA encoded by CSH1 [chorionic somatomammotropin hormone 1 (placental lactogen)], miR-141 was even more stable in maternal plasma, and its concentration did not decrease after filtration.
We have demonstrated the existence of placental miRNAs in maternal plasma and provide some information on their stability and physical nature. These findings open up a new class of molecular markers for pregnancy monitoring.
母体血浆中循环胎儿核酸的发现为无创产前诊断开辟了新的可能性。微小RNA(miRNA)是一类小RNA,由于其在基因表达中起重要调节作用,近来受到了深入研究。因为胎盘来源的核酸会释放到母体血浆中,我们推测胎盘产生的miRNA也会释放到母体血浆中。
我们系统地在母体血浆中寻找胎盘miRNA,以鉴定与母体血细胞相比在胎盘中浓度较高的miRNA,然后研究这类新型妊娠相关标志物在母体血浆中的稳定性和可过滤性。
在一组可用于157种成熟miRNA的TaqMan微小RNA检测中,有17种在胎盘中的浓度比母体血细胞中高10倍以上,且在产后母体血浆中无法检测到。这些胎盘中最丰富的4种miRNA(miR-141、miR-149、miR-299-5p和miR-135b)在孕期母体血浆中可检测到,而在产后血浆中的检测率降低。随着妊娠进入晚期,miR-141的血浆浓度升高。与CSH1[绒毛膜生长催乳素1(胎盘催乳素)]编码的mRNA相比,miR-141在母体血浆中更稳定,过滤后其浓度也没有降低。
我们已经证明母体血浆中存在胎盘miRNA,并提供了一些关于其稳定性和物理性质的信息。这些发现为妊娠监测开辟了一类新的分子标志物。