Mohamed Hisham, Turner James N, Caggana Michele
Wadsworth Center, New York State Department of Health, Albany, NY 12201-0509, USA.
J Chromatogr A. 2007 Aug 31;1162(2):187-92. doi: 10.1016/j.chroma.2007.06.025. Epub 2007 Jun 22.
Isolation of fetal cells from maternal circulation is the subject of intense research to eliminate the need for currently used invasive prenatal diagnosis procedures. Fetal cells can be isolated using magnetic-activated cell sorting or fluorescence-activated cell sorting, however no technique to specifically isolate and use fetal cells for genetic diagnosis has reached routine clinical practice. This paper demonstrates the use of a micromachined device to separate fetal cells from maternal circulation based on differences in size and deformation characteristics. Nucleated fetal red blood cells range in diameter from 9 to 12 microm can deform and pass through a channel as small as 2.5 microm wide and 5 microm deep. Although the white blood cells range in diameter from 10 to 20 microm, they cannot deform and are retained by the 2.5 microm wide and 5 microm deep channels under our experimental conditions. Fetal cells were isolated from cord blood and DNA analysis confirmed their fetal origin with ruled out maternal contamination.
从母体循环中分离胎儿细胞是一项深入研究的课题,旨在消除目前使用的侵入性产前诊断程序的必要性。可以使用磁激活细胞分选或荧光激活细胞分选来分离胎儿细胞,然而,尚无专门用于分离胎儿细胞并将其用于基因诊断的技术达到常规临床应用阶段。本文展示了一种微机械装置的应用,该装置基于大小和变形特征的差异从母体循环中分离胎儿细胞。有核胎儿红细胞直径在9至12微米之间,能够变形并通过宽度小至2.5微米、深度为5微米的通道。尽管白细胞直径在10至20微米之间,但在我们的实验条件下,它们无法变形,并被宽度为2.5微米、深度为5微米的通道截留。从脐带血中分离出胎儿细胞,DNA分析证实了它们的胎儿来源,排除了母体污染。