van Wijk I J, van Vugt J M, Mulders M A, Könst A A, Weima S M, Oudejans C B
Molecular Biology Laboratory, Department of Clinical Chemistry, Free University Hospital, Amsterdam, The Netherlands.
Am J Obstet Gynecol. 1996 Mar;174(3):871-8. doi: 10.1016/s0002-9378(96)70315-0.
Fetal cells circulate in the maternal blood during early pregnancy. Because these cells are rare, noninvasive prenatal diagnosis from fetal cells can be achieved only after efficient enrichment procedures. Our aim was to develop a two-step enrichment procedure to isolate trophoblast cells from 20 ml of peripheral blood.
Blood was obtained from pregnant women between 6 and 15 weeks of gestation, before invasive procedures were performed. After enrichment, the success of isolating fetal cells was determined by amplification of Y chromosome sequences.
A highly specific X/Y polymerase chain reaction was established, sensitive enough to detect X and Y chromosome-specific sequences in one single cell and in one male among 100,000 female cells. Sex determination by polymerase chain reaction was compared with results from conventional karyotyping. The success rate was 91.7%.
Enrichment of trophoblast cells from maternal blood as described here might be useful for early noninvasive prenatal diagnosis.
在妊娠早期,胎儿细胞会在母体血液中循环。由于这些细胞数量稀少,只有经过有效的富集程序后,才能从胎儿细胞中实现非侵入性产前诊断。我们的目标是开发一种两步富集程序,从20毫升外周血中分离滋养层细胞。
在进行侵入性操作之前,从妊娠6至15周的孕妇身上采集血液。富集后,通过Y染色体序列扩增来确定分离胎儿细胞的成功率。
建立了一种高度特异性的X/Y聚合酶链反应,其灵敏度足以在单个细胞以及100,000个雌性细胞中的一个雄性细胞中检测到X和Y染色体特异性序列。将聚合酶链反应的性别鉴定结果与传统核型分析结果进行比较。成功率为91.7%。
本文所述的从母体血液中富集滋养层细胞的方法可能对早期非侵入性产前诊断有用。