Characterization of placenta-specific microRNAs in fetal growth restriction pregnancy

被引:134
作者
Higashijima, Ai [1 ]
Miura, Kiyonori [1 ]
Mishima, Hiroyuki [1 ]
Kinoshita, Akira [1 ]
Jo, Ozora [1 ]
Abe, Shuhei [1 ]
Hasegawa, Yuri [1 ]
Miura, Shoko [1 ]
Yamasaki, Kentaro [1 ]
Yoshida, Atsushi [1 ]
Yoshiura, Koh-ichiro [1 ]
Masuzaki, Hideaki [1 ]
机构
[1] Nagasaki Univ, Grad Sch Biomed Sci, Nagasaki 852, Japan
基金
日本学术振兴会;
关键词
MATERNAL PLASMA; IDENTIFICATION; CIRCULATION; EXPRESSION; PREECLAMPSIA; RNAS;
D O I
10.1002/pd.4045
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Objective The aim of this study was to characterize placenta-specific microRNAs in fetal growth restriction (FGR) pregnancy. Method Placenta-specific miRNAs were identified by next-generation sequencing analysis. Subsequently, quantitative real-time reverse-transcription polymerase chain reaction was used to identify FGR placenta-specific miRNAs whose level of expression was significantly decreased in FGR placenta (n=45) compared with uncomplicated placenta (n=50). FGR pregnancy-associated, placenta-specific microRNAs were identified in maternal plasma after delivery at significantly decreased concentrations, and their circulating levels in maternal plasma was compared between FGR pregnancies (n=10) and uncomplicated pregnancies (n=10). Results Out of the ten placenta-specific microRNAs that we identified, seven placenta-specific microRNAs (hsa-miR-518b, hsa-miR-1323, hsa-miR-516b, hsa-miR-515-5p, hsa-miR-520h, hsa-miR-519d, and hsa-miR-526b) from the chromosome 19 microRNA cluster were identified as FGR placenta-specific microRNAs. Four FGR placenta-specific microRNAs (hsa-miR-518b, hsa-miR-1323, hsa-miR-520h, and hsa-miR-519d) were confirmed as FGR pregnancy-associated, placenta-specific miRNAs, but their circulating levels in maternal plasma showed no significant differences between FGR pregnancy and uncomplicated pregnancy. Conclusion Our data suggest that reduced expression in placenta of certain FGR placenta-specific miRNAs is associated with FGR and that the discrepancy between expression in FGR placenta and their circulating levels in maternal plasma will be crucial to understanding how placenta-specific microRNAs are released into the maternal circulation. (c) 2013 John Wiley & Sons, Ltd.
引用
收藏
页码:214 / 222
页数:9
相关论文
共 34 条
[1]   Growth and body composition in very young SGA children [J].
Argente, Jesus ;
Mehls, Otto ;
Barrios, Vicente .
PEDIATRIC NEPHROLOGY, 2010, 25 (04) :679-685
[2]   Bisphenol A exposure leads to specific microRNA alterations in placental cells [J].
Avissar-Whiting, Michele ;
Veiga, Keila R. ;
Uhl, Kristen M. ;
Maccani, Matthew A. ;
Gagne, Luc A. ;
Moen, Erika L. ;
Marsit, Carmen J. .
REPRODUCTIVE TOXICOLOGY, 2010, 29 (04) :401-406
[3]   Identification of hundreds of conserved and nonconserved human microRNAs [J].
Bentwich, I ;
Avniel, A ;
Karov, Y ;
Aharonov, R ;
Gilad, S ;
Barad, O ;
Barzilai, A ;
Einat, P ;
Einav, U ;
Meiri, E ;
Sharon, E ;
Spector, Y ;
Bentwich, Z .
NATURE GENETICS, 2005, 37 (07) :766-770
[4]   Anti-inflammatory therapy in an ovine model of fetal hypoxia induced by single umbilical artery ligation [J].
Bertucci, Micka C. ;
Loose, Jan M. ;
Wallace, Euan M. ;
Jenkin, Graham ;
Miller, Suzanne L. .
REPRODUCTION FERTILITY AND DEVELOPMENT, 2011, 23 (02) :346-352
[5]   Detection and characterization of placental MicroRNAs in maternal plasma [J].
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 .
CLINICAL CHEMISTRY, 2008, 54 (03) :482-490
[6]   Pregnancy-Associated MicroRNAs in Maternal Plasma: A Channel for Fetal-Maternal Communication? [J].
Chiu, Rossa W. K. ;
Lo, Y. M. Dennis .
CLINICAL CHEMISTRY, 2010, 56 (11) :1656-1657
[7]   Do DNA microarrays have their future behind them? [J].
Coppee, Jean-Yves .
MICROBES AND INFECTION, 2008, 10 (09) :1067-1071
[8]   Microparticles: major transport vehicles for distinct microRNAs in circulation [J].
Diehl, Philipp ;
Fricke, Alba ;
Sander, Laura ;
Stamm, Johannes ;
Bassler, Nicole ;
Htun, Nay ;
Ziemann, Mark ;
Helbing, Thomas ;
El-Osta, Assam ;
Jowett, Jeremy B. M. ;
Peter, Karlheinz .
CARDIOVASCULAR RESEARCH, 2012, 93 (04) :633-644
[9]   Restricted fetal growth in sudden intrauterine unexplained death [J].
Froen, JF ;
Gardosi, JO ;
Thurmann, A ;
Francis, A ;
Stray-Pedersen, B .
ACTA OBSTETRICIA ET GYNECOLOGICA SCANDINAVICA, 2004, 83 (09) :801-807
[10]  
Ghidini A, 1996, Obstet Gynecol Surv, V51, P376, DOI 10.1097/00006254-199606000-00023