Detection and characterization of placental microRNAs in maternal plasma
- PMID: 18218722
- DOI: 10.1373/clinchem.2007.097972
Detection and characterization of placental microRNAs in maternal plasma
Abstract
Background: 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.
Methods: 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.
Results: 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.
Conclusion: 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.
Similar articles
-
Dysregulation of Placental miRNA in Maternal Obesity Is Associated With Pre- and Postnatal Growth.J Clin Endocrinol Metab. 2017 Jul 1;102(7):2584-2594. doi: 10.1210/jc.2017-00089. J Clin Endocrinol Metab. 2017. PMID: 28368446
-
Identification of pregnancy-associated microRNAs in maternal plasma.Clin Chem. 2010 Nov;56(11):1767-71. doi: 10.1373/clinchem.2010.147660. Epub 2010 Aug 20. Clin Chem. 2010. PMID: 20729298
-
Characterization of placenta-specific microRNAs in fetal growth restriction pregnancy.Prenat Diagn. 2013 Mar;33(3):214-22. doi: 10.1002/pd.4045. Epub 2013 Jan 27. Prenat Diagn. 2013. PMID: 23354729
-
Circulating microRNAs as clinical biomarkers in the predictions of pregnancy complications.Biomed Res Int. 2015;2015:294954. doi: 10.1155/2015/294954. Epub 2015 Jan 29. Biomed Res Int. 2015. PMID: 25699269 Free PMC article. Review.
-
MicroRNAs in Pregnancy and Gestational Diabetes Mellitus: Emerging Role in Maternal Metabolic Regulation.Curr Diab Rep. 2017 May;17(5):35. doi: 10.1007/s11892-017-0856-5. Curr Diab Rep. 2017. PMID: 28378294 Review.
Cited by
-
Circulating miRNAs: cell-cell communication function?Front Genet. 2013 Jun 28;4:119. doi: 10.3389/fgene.2013.00119. Print 2013. Front Genet. 2013. PMID: 23825476 Free PMC article.
-
The Role of Cluster C19MC in Pre-Eclampsia Development.Int J Mol Sci. 2022 Nov 10;23(22):13836. doi: 10.3390/ijms232213836. Int J Mol Sci. 2022. PMID: 36430313 Free PMC article. Review.
-
MicroRNA profiling: approaches and considerations.Nat Rev Genet. 2012 Apr 18;13(5):358-69. doi: 10.1038/nrg3198. Nat Rev Genet. 2012. PMID: 22510765 Free PMC article. Review.
-
The potential of circulating extracellular small RNAs (smexRNA) in veterinary diagnostics-Identifying biomarker signatures by multivariate data analysis.Biomol Detect Quantif. 2015 Sep 19;5:15-22. doi: 10.1016/j.bdq.2015.08.001. eCollection 2015 Sep. Biomol Detect Quantif. 2015. PMID: 27077039 Free PMC article.
-
EVs-miRNA: The New Molecular Markers for Chronic Respiratory Diseases.Life (Basel). 2022 Oct 5;12(10):1544. doi: 10.3390/life12101544. Life (Basel). 2022. PMID: 36294979 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical