A microfluidics approach for the isolation of nucleated red blood cells (NRBCs) from the peripheral blood of pregnant women

被引:122
作者
Huang, R. [1 ]
Barber, T. A. [1 ]
Schmidt, M. A. [2 ]
Tompkins, R. G. [3 ,4 ]
Toner, M. [3 ,4 ]
Bianchi, D. W. [5 ]
Kapur, R. [1 ]
Flejter, W. L. [1 ]
机构
[1] Artemis Hlth Inc, Menlo Pk, CA USA
[2] MIT, Cambridge, MA 02139 USA
[3] Harvard Univ, Sch Med, Massachusetts Gen Hosp, BioMicroElectroMech Syst Resource Ctr & Surg Serv, Boston, MA USA
[4] Shriners Hosp Children, Boston, MA USA
[5] Tufts Univ, Sch Med, Dept Pediat, Boston, MA 02111 USA
关键词
microfluidcs; nucleated red blood cells; noninvasive prenatal diagnosis;
D O I
10.1002/pd.2079
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学]; 090102 [作物遗传育种];
摘要
Objective Nucleated red blood cells (NRBCs) have been identified in maternal circulation and potentially provide a resource for the monitoring and diagnosis of maternal, fetal, and neonatal health and disease. Past strategies used to isolate and enrich for NRBCs are limited to complex approaches that result in low recovery and less than optiamal cell purity. Here we report the development of a high-throughput and highly efficient microfluidic device for isolating rare NRBCs from maternal blood. Material and Methods NRBCs were isolated from the peripheral blood of 58 pregnant women using a microfluidic process that consists of a microfluidic chip for size-based cell separation and a magnetic device her hemoglobin-based cell isolation. Results The microfluidic-magnetic combination removes nontarget red blood cells and white blood cells at a very high efficiency (similar to 99.99%). The device successfully identified NRBCs from the peripheral blood of 58/58 pretermination samples with a mean of 37.44 NRBC/mL (range 0.37-274.36 NRBC/mL). These results were compared with those from previous studies. Conclusion The microfluidic device results in an approximate 10- to 20-fold enrichment of NRBCs over methods described previously. The reliability of isolation and the purity of the NRBC product have the potential to enable the subsequent application of molecular diagnostic assays. Copyright (C) 2008 John Wiley & Sons, Ltd.
引用
收藏
页码:892 / 899
页数:8
相关论文
共 36 条
[1]
Evaluation of a soybean lectin-based method for the enrichment of erythroblasts [J].
Babochkina, T ;
Mergenthaler, S ;
Lapaire, O ;
Kiefer, V ;
Yura, H ;
Koike, K ;
Holzgreve, W ;
Hahn, S .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 2005, 53 (03) :329-330
[2]
Fetal gender and aneuploidy detection using fetal cells in maternal blood: analysis of NIFTY I data [J].
Bianchi, DW ;
Simpson, JL ;
Jackson, LG ;
Elias, S ;
Holzgreve, W ;
Evans, MI ;
Dukes, KA ;
Sullivan, LM ;
Klinger, KW ;
Bischoff, FZ ;
Hahn, S ;
Johnson, KL ;
Lewis, D ;
Wapner, RJ .
PRENATAL DIAGNOSIS, 2002, 22 (07) :609-615
[3]
ISOLATION OF FETAL DNA FROM NUCLEATED ERYTHROCYTES IN MATERNAL BLOOD [J].
BIANCHI, DW ;
FLINT, AF ;
PIZZIMENTI, MF ;
KNOLL, JHM ;
LATT, SA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (09) :3279-3283
[4]
PCR quantitation of fetal cells in maternal blood in normal and aneuploid pregnancies [J].
Bianchi, DW ;
Williams, JM ;
Sullivan, LM ;
Hanson, FW ;
Klinger, KW ;
Shuber, AP .
AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 61 (04) :822-829
[5]
ENRICHMENT OF FETAL CELLS FROM MATERNAL BLOOD BY HIGH-GRADIENT MAGNETIC CELL SORTING (DOUBLE MACS) FOR PCR-BASED GENETIC-ANALYSIS [J].
BUSCH, J ;
HUBER, P ;
PFLUGER, E ;
MILTENYI, S ;
HOLTZ, J ;
RADBRUCH, A .
PRENATAL DIAGNOSIS, 1994, 14 (12) :1129-1140
[6]
Campagnoli C, 1997, J REPROD MED, V42, P193
[7]
de Graaf IM, 1999, PRENATAL DIAG, V19, P648, DOI 10.1002/(SICI)1097-0223(199907)19:7<648::AID-PD600>3.0.CO
[8]
2-X
[9]
Fetal cells in maternal blood: A six-fold increase in women who have undergone amniocentesis and carry a fetus with Down syndrome: A multicenter study [J].
Falcidia, E ;
Parano, E ;
Grillo, A ;
Pavone, P ;
Takabayashi, H ;
Trifiletti, RR ;
Scollo, P ;
Dallapiccola, B ;
Grammatico, P ;
Novelli, A ;
Paladini, D ;
Monni, G ;
Gulisano, A ;
Scassellati, G .
NEUROPEDIATRICS, 2004, 35 (06) :321-324
[10]
GANSHIRTAHLERT D, 1992, AM J OBSTET GYNECOL, V166, P1350