Document Detail

High frequency of fetal cells within a primitive stem cell population in maternal blood.
MedLine Citation:
PMID:  18238907     Owner:  NLM     Status:  MEDLINE    
BACKGROUND: During pregnancy, fetal cells enter the maternal bloodstream resulting in fetal cell microchimerism. The fetal cells persist in the mother for decades and colonize a variety of maternal organs. They are associated with maternal autoimmune diseases and may also participate in tissue repair. The identity of the microchimeric cells is not certain but they must be able to persist long-term and have potential for multitissue differentiation. METHODS AND RESULTS: Here we tested the hypothesis that the fetal microchimeric cells are primitive stem cells, represented by CD34+ adherent cells, which have a wide potential for differentiation. We isolated these stem cells from the blood of pregnant females (n = 25) and detected fetal cells of the correct gender, using fluorescence in situ hybridization, in a high proportion (71% male fetuses and 90% female fetuses; false positive rate 11%, false negative rate 29%) of cases. By RT-PCR, we demonstrated that the cells express Oct-4, Nanog and Rex-1. No fetal cells were detected in the mononuclear or total CD34+ cell populations but high frequencies (mean 11.8%) of fetal cells were detected in the adherent CD34+ cell population. CONCLUSIONS: These results identify adherent CD34+ stem cells as candidate fetal microchimeric cells, which are capable of sustaining the fetal cell population in the long term and have the ability to colonize multiple tissues and organs.
Magued A Mikhail; Hanane M'Hamdi; Jonathan Welsh; Natasa Levicar; Stephen B Marley; Joanna P Nicholls; Nagy A Habib; Louay S Louis; Nicholas M Fisk; Myrtle Y Gordon
Related Documents :
12473207 - Cml leukapheresis products can be enriched for cd34+ cells and simultaneously depleted ...
18770857 - Flow cytometry of the side population (sp).
9103417 - Prethymic cd34+ progenitors capable of developing into t cells are not committed to the...
11602407 - Engraftment potential into nod/scid mice of cd34+ cells derived from human fetal liver ...
2302737 - Early production of a chemotactic factor to t lymphocytes by peritoneal macrophages.
22701517 - An initial in vitro investigation into the potential therapeutic use of supt1 cells to ...
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't     Date:  2008-01-31
Journal Detail:
Title:  Human reproduction (Oxford, England)     Volume:  23     ISSN:  1460-2350     ISO Abbreviation:  Hum. Reprod.     Publication Date:  2008 Apr 
Date Detail:
Created Date:  2008-03-19     Completed Date:  2008-05-27     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  8701199     Medline TA:  Hum Reprod     Country:  England    
Other Details:
Languages:  eng     Pagination:  928-33     Citation Subset:  IM    
Department of Surgery, Imperial College London, Faculty of Medicine, Hammersmith Campus, Du Cane Road, London W12 0NN, UK.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Antigens, CD34
Case-Control Studies
Child, Preschool
Fetus / cytology*
Maternal-Fetal Exchange / physiology*
Reverse Transcriptase Polymerase Chain Reaction
Stem Cells / cytology*
Reg. No./Substance:
0/Antigens, CD34

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Previous Document:  Integrity rate of pronuclei after cryopreservation of pronuclear-zygotes as a criteria for subsequen...
Next Document:  ESHRE PGD consortium data collection VII: cycles from January to December 2004 with pregnancy follow...