Skip Navigation

This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (28)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Zhong, X. Y.
Right arrow Articles by Hahn, S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Zhong, X. Y.
Right arrow Articles by Hahn, S.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Molecular Human Reproduction, Vol. 8, No. 9, 864-870, September 2002
© 2002 European Society of Human Reproduction and Embryology


Implantation and pregnancy

Cell-free fetal DNA in the maternal circulation does not stem from the transplacental passage of fetal erythroblasts

Xiao Yan Zhong, Wolfgang Holzgreve and Sinuhe Hahn,1

1 Laboratory for Prenatal Medicine, Department of Obstetrics and Gynecology, University of Basel, Schanzenstrasse 46, CH 4031, Switzerland

Fetal cells, specifically fetal erythroblasts, as well as cell-free fetal DNA are present in the maternal circulation. Both are currently being investigated as a means for the non-invasive risk-free analysis of fetal genetic traits. The origin of this cell-free fetal DNA in the maternal circulation is currently unclear. Since numerous fetal erythroblasts have been demonstrated to exhibit an apoptotic phenotype in the form of fragmented nuclear DNA, it has been proposed that such trafficking fetal cells may be a possible source. This hypothesis is supported by reports of elevated numbers of fetal erythroblast and cell-free fetal DNA concentrations in pregnancies affected by pre-eclampsia or polyhydramnios. To address this question, we have examined fetal erythroblast numbers and cell-free DNA concentrations in the same maternal blood samples. Our study, performed on both normal and pathologically-affected pregnancies, indicates that no correlation exists between these two fetal cellular and molecular species. This is most evident in pregnancies affected by onset of preterm labour, where significant elevations in cell-free fetal DNA concentrations were detected without any concomitant elevation in fetal erythroblast numbers. Our data therefore suggest that an alternative cell type is the source of cell-free fetal DNA. Furthermore, it appears that the release of cell-free fetal DNA from this cell type is affected by pathological placental conditions which are not associated with an increase in fetal cell trafficking.

fetal cells/fetal DNA/maternal blood

1 To whom correspondence should be addressed. E-mail: shahn{at}uhbs.ch


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Ann. N. Y. Acad. Sci.Home page
Y. LI, W. HOLZGREVE, E. DI NARO, A. VITUCCI, and S. HAHN
Cell-Free DNA in Maternal Plasma: Is It All a Question of Size?
Ann. N.Y. Acad. Sci., September 1, 2006; 1075: 81 - 87.
[Abstract] [Full Text] [PDF]


Home page
Ann. N. Y. Acad. Sci.Home page
A. FARINA, M. CONCU, I. BANZOLA, A. TEMPESTA, S. VAGNONI, S. GABRIELLI, M. MATTIOLI, P. CARINCI, G. PILU, D. MORANO, et al.
PLAC1 mRNA in Maternal Blood Correlates with Doppler Waveform in Uterine Arteries in Normal Pregnancies at the Second and Third Trimester.
Ann. N.Y. Acad. Sci., September 1, 2006; 1075: 130 - 136.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Pathol.Home page
M. L. Tjoa, T. Cindrova-Davies, O. Spasic-Boskovic, D. W. Bianchi, and G. J. Burton
Trophoblastic Oxidative Stress and the Release of Cell-Free Feto-Placental DNA
Am. J. Pathol., August 1, 2006; 169(2): 400 - 404.
[Abstract] [Full Text] [PDF]


Home page
Hum Reprod UpdateHome page
F. Z. Bischoff, D. E. Lewis, and J. L. Simpson
Cell-free fetal DNA in maternal blood: kinetics, source and structure
Hum. Reprod. Update, January 1, 2005; 11(1): 59 - 67.
[Abstract] [Full Text] [PDF]


Home page
Ann. N. Y. Acad. Sci.Home page
T. WATAGANARA and D. W. BIANCHI
Fetal Cell-Free Nucleic Acids in the Maternal Circulation: New Clinical Applications
Ann. N.Y. Acad. Sci., June 1, 2004; 1022(1): 90 - 99.
[Abstract] [Full Text] [PDF]


Home page
Hum ReprodHome page
E. Flori, B. Doray, E. Gautier, M. Kohler, P. Ernault, J. Flori, and J.M. Costa
Circulating cell-free fetal DNA in maternal serum appears to originate from cyto- and syncytio-trophoblastic cells. Case report
Hum. Reprod., March 1, 2004; 19(3): 723 - 724.
[Abstract] [Full Text] [PDF]


Home page
Clin. Chem.Home page
M. Smid, S. Galbiati, A. Vassallo, D. Gambini, A. Ferrari, G. Restagno, E. Viora, M. Pagliano, S. Calza, M. Ferrari, et al.
Fetal DNA in Maternal Plasma in Twin Pregnancies
Clin. Chem., September 1, 2003; 49(9): 1526 - 1528.
[Full Text] [PDF]


Home page
Clin. Chem.Home page
L. Y.S. Chan, T. N. Leung, K.C. A. Chan, H.-L. Tai, T. K. Lau, E. M.C. Wong, and Y.M. D. Lo
Serial Analysis of Fetal DNA Concentrations in Maternal Plasma in Late Pregnancy
Clin. Chem., April 1, 2003; 49(4): 678 - 680.
[Full Text] [PDF]


Home page
Obstet GynecolHome page
I. Hoesli, M. Danek, D. Lin, Y. Li, S. Hahn, and W. Holzgreve
Circulating Erythroblasts in Maternal Blood Are Not Elevated Before Onset of Preterm Labor
Obstet. Gynecol., November 1, 2002; 100(5): 992 - 996.
[Abstract] [Full Text] [PDF]



Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.