Optimized RNA extraction from non-deparaffinized, laser-microdissected material

Methods Mol Biol. 2011:755:67-75. doi: 10.1007/978-1-61779-163-5_5.

Abstract

mRNA extraction and subsequent RT-polymerase chain reaction (PCR)-based expression analysis from laser-microdissected material is by now a well-established and reproducible method. Most routinely stored tissue samples are preserved as formalin-fixed, paraffin-embedded materials. While this allows for a convenient storage and stable preservation of nucleic acids, deparaffinization before staining for laser microdissection may result in a significant loss of mRNA quality and consequently of PCR sensitivity. We describe a method of isolating anatomic compartments from non-deparaffinized, formalin-fixed, and paraffin-embedded tissues by laser-assisted microdissection which allows for a highly efficient mRNA retrieval.

MeSH terms

  • Cell Separation / methods
  • Data Interpretation, Statistical
  • Gene Expression
  • Gene Expression Profiling / methods
  • Genes, Wilms Tumor
  • Humans
  • Kidney Glomerulus / cytology
  • Kidney Glomerulus / metabolism
  • Lasers*
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism
  • Microdissection / methods*
  • Microtomy / methods
  • Paraffin Embedding*
  • Pulmonary Veins / cytology
  • RNA Polymerase II / genetics
  • RNA Polymerase II / metabolism
  • RNA, Messenger / genetics
  • RNA, Messenger / isolation & purification*
  • Reverse Transcriptase Polymerase Chain Reaction / methods
  • Tissue Fixation / methods
  • Umbilical Arteries / cytology

Substances

  • Membrane Proteins
  • RNA, Messenger
  • nephrin
  • RNA Polymerase II