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Soper, Steven A.
Soper Research Group
Research Interests
  • Micro- and nano-fabrication

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Parallel affinity-based isolation of leukocyte subsets using microfluidics: Application for stroke diagnosis

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Title
Parallel affinity-based isolation of leukocyte subsets using microfluidics: Application for stroke diagnosis
Author
Pullagurla, Swathi R.Witek, Małgorzata A.Jackson, Joshua M.Lindell, Maria A. M.Hupert, Mateusz L.Nesterova, Irina V.Baird, Alison E.Soper, Steven A.
Keywords
ACUTE ISCHEMIC-STROKE; BLOOD MONONUCLEAR-CELLS; GENE-EXPRESSION PROFILE; CD4(+) T-LYMPHOCYTES; PERIPHERAL-BLOOD; HIGHLY EFFICIENT; DENDRITIC CELLS; WHOLE-BLOOD; BIOMARKERS; SEQUENCE
Issue Date
201404
Publisher
AMER CHEMICAL SOC
Citation
ANALYTICAL CHEMISTRY, v.86, no.8, pp.4058 - 4065
Abstract
We report the design and performance of a polymer microfluidic device that can affinity select multiple types of biological cells simultaneously with sufficient recovery and purity to allow for the expression profiling of mRNA isolated from these cells. The microfluidic device consisted of four independent selection beds with curvilinear channels that were 25 μm wide and 80 μm deep and were modified with antibodies targeting antigens specifically expressed by two different cell types. Bifurcated and Z-configured device geometries were evaluated for cell selection. As an example of the performance of these devices, CD4+ T-cells and neutrophils were selected from whole blood as these cells are known to express genes found in stroke-related expression profiles that can be used for the diagnosis of this disease. CD4+ T-cells and neutrophils were simultaneously isolated with purities >90% using affinity-based capture in cyclic olefin copolymer (COC) devices with a processing time of ∼3 min. In addition, sufficient quantities of the cells could be recovered from a 50 μL whole blood input to allow for reverse transcription-polymerase chain reaction (RT-PCR) following cell lysis. The expression of genes from isolated T-cells and neutrophils, such as S100A9, TCRB, and FPR1, was evaluated using RT-PCR. The modification and isolation procedures demonstrated here can also be used to analyze other cell types as well where multiple subsets must be interrogated.
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DOI
http://dx.doi.org/10.1021/ac5007766
ISSN
0003-2700
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