Trophoblast-like cells sorted from peripheral maternal blood using flow cytometry: A multiparametric study involving transmission electron microscopy and fetal dna amplification |
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Authors: | Dr. J. F. Bruch P. Metezeau N. Garcia-Fonknechten Y. Richard V. Tricottet B.-L. Hsi A. Kitzis C. Julien E. Papiernik |
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Affiliation: | 1. Service Cornmun INSERM No. 9, Institut Pasteur, 75015, Paris;2. Institut de Pathologic Moleculaire, CHU Cochin, 75014, Paris;3. Unité INSERM U131,92140, Clamart;4. Laboratoire Central d'Anatomie-Pathologique, Hǒpital Paul Brousse, 94800, Villejuif;5. Unité INSERM U210, Faculté de Médecine de Nice, 06000 Nice;6. Coulter-Coultronics S.A., 95580 Margency;7. Unité INSERM U187, 92140, Clamart, France |
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Abstract: | Three monoclonal antibodies (MAbs) against trophoblast (GB17, GB21, and GB25) and flow cytometry were used to sort trophoblast-like cells (TLCs) from peripheral blood of pregnant women. Sorted TLCs were processed for electron microscopy and fetal DNA amplification of the Y-specific sequences from mothers carrying male fetuses. At the ultra-structural level, most of the nucleated cells had the morphology of leucocytes, suggesting maternal contaminants, and we did not find the characteristic features of the free inter-villous trophoblast cells. Nevertheless, polymerase chain reaction (PCR) analysis showed an amplification of Y-specific sequences in two out of three samples of sorted TLCs. These results suggest that besides the maternal leucocytes, sufficient trophoblast nucleated fetal cells can be obtained using cell enrichment by sorting. This sensitive method holds promise for non-invasive prenatal diagnosis of fetal sex and if sufficient Y(positive) nuclei are found, for the diagnosis of selected numerical chromosome abnormalities. |
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Keywords: | Trophoblast monoclonal antibodies Cell sorting Electron microscopy Fetal DNA amplification Prenatal diagnosis Fetal cells from maternal blood |
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