4.5 Review

The workflow of single-cell expression profiling using quantitative real-time PCR

Journal

EXPERT REVIEW OF MOLECULAR DIAGNOSTICS
Volume 14, Issue 3, Pages 323-331

Publisher

TAYLOR & FRANCIS AS
DOI: 10.1586/14737159.2014.901154

Keywords

single-cell workflow; gene expression profiling; RT-qPCR; single-cell analysis; preamplification; single-cell biology

Categories

Funding

  1. Assar Gabrielssons Research Foundation
  2. BioCARE National Strategic Research Program at University of Gothenburg
  3. LUA/ALF Vastra Gotaland
  4. Johan Jansson Foundation for Cancer Research
  5. Swedish Cancer Society
  6. Swedish Society for Medical Research
  7. Swedish Research Council [521-2011-2367]
  8. Wilhelm and Martina Lundgren Foundation for Scientific Research
  9. Grant Agency of the Czech Republic
  10. BIOCEV [CZ.1.05/1.1.00/02.0109, ERDF]
  11. [GA13-02154S]

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Biological material is heterogeneous and when exposed to stimuli the various cells present respond differently. Much of the complexity can be eliminated by disintegrating the sample, studying the cells one by one. Single-cell profiling reveals responses that go unnoticed when classical samples are studied. New cell types and cell subtypes may be found and relevant pathways and expression networks can be identified. The most powerful technique for single-cell expression profiling is currently quantitative reverse transcription real-time PCR (RT-qPCR). A robust RT-qPCR workflow for highly sensitive and specific measurements in high-throughput and a reasonable degree of multiplexing has been developed for targeting mRNAs, but also microRNAs, non-coding RNAs and most recently also proteins. We review the current state of the art of single-cell expression profiling and present also the improvements and developments expected in the next 5 years.

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