Hromadníková I, Bendukidze N, Mrstinová M, Ivasková E
2nd Clinic of Paediatrics, University Hospital Motol, Prague, Czech Republic.
Folia Biol (Praha). 2001;47(1):36-9.
The purpose of our study was to identify paternal alleles in NRBC enriched from maternal peripheral blood for detection of the presence of foetal cells in the maternal circulation and to establish a reliable non-invasive method which should allow following genetic testing. For enrichment of foetal cells from peripheral maternal blood we combined Ficoll-Paque density gradient centrifugation and MACS. Maternal leukocytes were firstly depleted using anti-CD14 and anti-CD45 microbeads. NRBC were sorted from the CD14-/CD45- fraction by positive selection using CD71 microbeads. Paternal alleles in the CD14-/CD45-/CD71+ fraction were indicated by the PCR method using HLA (DRB1, DQB1, DQA1) and Polymarker System (LDLR, GYPA, HBGG, D7S8, GC) as genetic markers. Different paternal alleles of studied 8 loci were detected in 13 out of 19 samples of cells enriched from maternal peripheral blood between the 13th and 36th week of gestation. Our results demonstrate that foetal cells enriched from maternal peripheral blood may be used as a source of foetal DNA for prenatal diagnosis, paternity testing and other application.
我们研究的目的是鉴定从母体外周血中富集的有核红细胞中的父系等位基因,以检测母体循环中胎儿细胞的存在,并建立一种可靠的非侵入性方法,以便进行后续的基因检测。为了从母体外周血中富集胎儿细胞,我们将Ficoll-Paque密度梯度离心法和磁珠细胞分选法相结合。首先使用抗CD14和抗CD45微珠去除母体白细胞。通过使用CD71微珠进行阳性选择,从CD14-/CD45-组分中筛选出有核红细胞。使用HLA(DRB1、DQB1、DQA1)和多标记系统(LDLR、GYPA、HBGG、D7S8、GC)作为遗传标记,通过PCR方法检测CD14-/CD45-/CD71+组分中的父系等位基因。在妊娠第13至36周期间,从19份母体外周血富集细胞样本中的13份中检测到了所研究的8个基因座的不同父系等位基因。我们的结果表明,从母体外周血中富集的胎儿细胞可作为胎儿DNA的来源,用于产前诊断、亲子鉴定和其他应用。