Placenta-derived exosomes continuously increase in maternal circulation over the first trimester of pregnancy

被引:375
作者
Sarker, Suchismita [1 ]
Scholz-Romero, Katherin [1 ]
Perez, Alejandra [2 ]
Illanes, Sebastian E. [1 ,2 ,3 ]
Mitchell, Murray D. [1 ]
Rice, Gregory E. [1 ,2 ]
Salomon, Carlos [1 ,2 ]
机构
[1] Univ Queensland, Royal Brisbane & Womens Hosp, UQ Ctr Clin Res, Ctr Clin Diagnost, Herston, Qld 4029, Australia
[2] Univ Los Andes, Dept Obstet & Gynaecol, Fac Med, Santiago, Chile
[3] Clin Davila, Perinatal Unit, Dept Obstet & Gynaecol, Santiago, Chile
关键词
Exosomes; Pregnancy; Placenta; Fetal-maternal exchange; SERUM ALKALINE-PHOSPHATASE; PLASMA; CELLS; BIOGENESIS; EXPRESSION; BIOMARKERS; ELEVATION; BLOOD; MIRNA;
D O I
10.1186/1479-5876-12-204
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
100103 [病原生物学]; 100218 [急诊医学];
摘要
Background: Human placenta releases specific nanovesicles (i.e. exosomes) into the maternal circulation during pregnancy, however, the presence of placenta-derived exosomes in maternal blood during early pregnancy remains to be established. The aim of this study was to characterise gestational age related changes in the concentration of placenta-derived exosomes during the first trimester of pregnancy (i.e. from 6 to 12 weeks) in plasma from women with normal pregnancies. Methods: A time-series experimental design was used to establish pregnancy-associated changes in maternal plasma exosome concentrations during the first trimester. A series of plasma were collected from normal healthy women (10 patients) at 6, 7, 8, 9, 10, 11 and 12 weeks of gestation (n = 70). We measured the stability of these vesicles by quantifying and observing their protein and miRNA contents after the freeze/thawing processes. Exosomes were isolated by differential and buoyant density centrifugation using a sucrose continuous gradient and characterised by their size distribution and morphology using the nanoparticles tracking analysis (NTA; Nanosight (TM)) and electron microscopy (EM), respectively. The total number of exosomes and placenta-derived exosomes were determined by quantifying the immunoreactive exosomal marker, CD63 and a placenta-specific marker (Placental Alkaline Phosphatase PLAP). Results: These nanoparticles are extraordinarily stable. There is no significant decline in their yield with the freeze/thawing processes or change in their EM morphology. NTA identified the presence of 50-150 nm spherical vesicles in maternal plasma as early as 6 weeks of pregnancy. The number of exosomes in maternal circulation increased significantly (ANOVA, p = 0.002) with the progression of pregnancy (from 6 to 12 weeks). The concentration of placenta-derived exosomes in maternal plasma (i.e. PLAP(+)) increased progressively with gestational age, from 6 weeks 70.6 +/- 5.7 pg/ml to 12 weeks 117.5 +/- 13.4 pg/ml. Regression analysis showed that weeks is a factor that explains for >70% of the observed variation in plasma exosomal PLAP concentration while the total exosome number only explains 20%. Conclusions: During normal healthy pregnancy, the number of exosomes present in the maternal plasma increased significantly with gestational age across the first trimester of pregnancy. This study is a baseline that provides an ideal starting point for developing early detection method for women who subsequently develop pregnancy complications, clinically detected during the second trimester. Early detection of women at risk of pregnancy complications would provide an opportunity to develop and evaluate appropriate intervention strategies to limit acute adverse sequel.
引用
收藏
页数:19
相关论文
共 42 条
[1]
APLIN JD, 1991, J CELL SCI, V99, P681
[2]
Morphologic and proteomic characterization of exosomes released by cultured extravillous trophoblast cells [J].
Atay, Safinur ;
Gercel-Taylor, Cicek ;
Kesimer, Mehmet ;
Taylor, Douglas D. .
EXPERIMENTAL CELL RESEARCH, 2011, 317 (08) :1192-1202
[3]
Positive placental staining for alkaline phosphatase corresponding with extreme elevation of serum alkaline phosphatase during pregnancy [J].
Bashiri A. ;
Katz O. ;
Maor E. ;
Sheiner E. ;
Pack I. ;
Mazor M. .
Archives of Gynecology and Obstetrics, 2007, 275 (3) :211-214
[4]
Human placental trophoblasts confer viral resistance to recipient cells [J].
Delorme-Axford, Elizabeth ;
Donker, Rogier B. ;
Mouillet, Jean-Francois ;
Chu, Tianjiao ;
Bayer, Avraham ;
Ouyang, Yingshi ;
Wang, Tianyi ;
Stolz, Donna B. ;
Sarkar, Saumendra N. ;
Morelli, Adrian E. ;
Sadovsky, Yoel ;
Coyne, Carolyn B. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2013, 110 (29) :12048-12053
[5]
The expression profile of C19MC microRNAs in primary human trophoblast cells and exosomes [J].
Donker, R. B. ;
Mouillet, J. F. ;
Chu, T. ;
Hubel, C. A. ;
Stolz, D. B. ;
Morelli, A. E. ;
Sadovsky, Yoel .
MOLECULAR HUMAN REPRODUCTION, 2012, 18 (08) :417-424
[6]
Multicolor Flow Cytometry and Nanoparticle Tracking Analysis of Extracellular Vesicles in the Plasma of Normal Pregnant and Pre-eclamptic Women [J].
Dragovic, Rebecca A. ;
Southcombe, Jennifer H. ;
Tannetta, Dionne S. ;
Redman, Christopher W. G. ;
Sargent, Ian L. .
BIOLOGY OF REPRODUCTION, 2013, 89 (06)
[7]
Placental insufficiency and its consequences [J].
Gagnon, R .
EUROPEAN JOURNAL OF OBSTETRICS GYNECOLOGY AND REPRODUCTIVE BIOLOGY, 2003, 110 :S99-S107
[8]
The Majority of MicroRNAs Detectable in Serum and Saliva Is Concentrated in Exosomes [J].
Gallo, Alessia ;
Tandon, Mayank ;
Alevizos, Ilias ;
Illei, Gabor G. .
PLOS ONE, 2012, 7 (03)
[9]
miRNA in Plasma Exosome is Stable under Different Storage Conditions [J].
Ge, Qinyu ;
Zhou, Youxia ;
Lu, Jiafeng ;
Bai, Yunfei ;
Xie, Xueying ;
Lu, Zuhong .
MOLECULES, 2014, 19 (02) :1568-1575
[10]
IN-VIVO INVESTIGATION OF THE PLACENTAL CIRCULATIONS BY DOPPLER ECHOGRAPHY [J].
JAUNIAUX, E ;
JURKOVIC, D ;
CAMPBELL, S .
PLACENTA, 1995, 16 (04) :323-331