4.8 Article

A microfluidic multiwell chip for enzyme-free detection of mRNA from few cells

Journal

BIOSENSORS & BIOELECTRONICS
Volume 86, Issue -, Pages 20-26

Publisher

ELSEVIER ADVANCED TECHNOLOGY
DOI: 10.1016/j.bios.2016.06.019

Keywords

Ultra-sensitive detection; mRNA expression; Microarray; Cellular heterogeneity; Lab-on-a-chip

Funding

  1. Austrian Science Fund [L422-N20]
  2. Austrian Research Promotion Agency (FFG) [844738]
  3. State of Upper Austria
  4. Priority Program Biosciences and Health of the Paris-Lodron University of Salzburg
  5. European Fund for Regional Development

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Isogenic cell populations possess heterogeneous gene expression patterns. Most methods for mRNA expression analysis start with the reverse transcription of mRNA into cDNA, a process.that can introduce strong signal variations not related to the actual mRNA levels. Miniaturized lab-on-a-chip systems offer properties - e.g. low sample dilution, low contamination that enable new reaction schemes for molecular analyses. To enable transcription-free mRNA expression analysis of few single cells, a one-step cell lysis, target labelling and hybridisation approach as well as a corresponding passive multiwell chip with a volume of 25.5 nL/well were developed. The method enabled the parallel analysis of up to 96 samples and 6 target genes per sample. Preceding light microscopy of the living cells allowed correlating mRNA levels and cell number. As a proof-of-principle, the pancreatic cancer cell line Panc-1 was investigated for expression heterogeneity of a reference gene plus 5 genes reported to be overexpressed in cancer stem cells (CSCs). A good correlation (r(51)=0.739, p < 0.001; rs(51)= 0.744, p < 0.001) between the cell number per well and the number of detected reference gene mRNA confirmed the proper function of the device. Moreover, a heterogeneous expression of the CSC-associated target genes was found which matched well with reports on the presence of CSCs in the Panc-1 cell line. (C) 2016 Elsevier B.V. All rights reserved.

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