Microfluidic isolation of leukocytes from whole blood for phenotype and gene expression analysis

被引:65
作者
Sethu, Palaniappan
Moldawer, Lyle L.
Mindrinos, Michael N.
Scumpia, Philip O.
Tannahill, Cynthia L.
Wilhelmy, Julie
Efron, Philip A.
Brownstein, Bernard H.
Tompkins, Ronald G.
Toner, Mehmet
机构
[1] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Surg Serv, Boston, MA 02114 USA
[2] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Ctr Engn Med, Boston, MA 02114 USA
[3] Shriners Hosp Children, Boston, MA 02114 USA
[4] Washington Univ, Sch Med, St Louis, MO 63101 USA
[5] Univ Florida, Coll Med, Dept Surg, Gainesville, FL 32610 USA
[6] Stanford Genome Technol Ctr, Palo Alto, CA 94304 USA
关键词
D O I
10.1021/ac060140c
中图分类号
O65 [分析化学];
学科分类号
070302 [分析化学]; 081704 [应用化学];
摘要
Technologies that enable the isolation of cell subtypes from small samples of complex populations will greatly facilitate the implementation of proteomics and genomics to human diseases. Transcriptome analysis of blood requires the depletion of contaminating erythrocytes. We report an automated microfluidic device to rapidly deplete erythrocytes from whole blood via deionized water lysis and to collect enriched leukocytes for phenotype and genomic analyses. Starting with blood from healthy subjects, we demonstrate the utility of this microfluidic cassette and lysis protocol to prepare unstimulated leukocytes, and leukocytes stimulated ex vivo with Staphylococcal enterotoxin B, which mimics some of the cellular effects seen in patients with severe bacterial infections. Microarrays are used to assess the global gene expression response to enterotoxin B. The results demonstrate that this system can isolate unactivated leukocytes from small blood samples without any significant loss, which permits more information to be obtained from subsequent analysis, and will be readily applicable to clinical settings.
引用
收藏
页码:5453 / 5461
页数:9
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