A polymerase chain reaction-based method for the semiquantitative study of interleukin-8 mRNA in human basophil leukocytes

Scand J Clin Lab Invest. 1995 Oct;55(6):487-93. doi: 10.1080/00365519509075386.

Abstract

We examined a potential method for quantitative analysis of cytokine expression patterns in purified human basophil leukocyte preparations. Basophil mRNA was reverse transcribed and cytokine cDNA levels determined by competitive polymerase chain reaction (PCR) with internal standard cDNAs constructed by site-directed mutagenesis. Co-reverse transcribed glyceraldehyde-3-phosphate-dehydrogenase (GAPDH) cDNA levels were used as an internal control to correct for unequal efficiencies in RNA isolation and reverse transcription. The method was subjected to a statistical validation giving the within series precision of the analysis. This method was used to examine interleukin-8 expression patterns in basophils from different donors. The results from this study revealed increased interleukin-8 mRNA levels after in vitro challenge with a variety of stimuli.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Basophils / chemistry*
  • DNA, Complementary / standards
  • Glyceraldehyde-3-Phosphate Dehydrogenases / genetics
  • Humans
  • Interleukin-8 / blood
  • Interleukin-8 / genetics*
  • Molecular Sequence Data
  • Polymerase Chain Reaction* / methods
  • Polymerase Chain Reaction* / standards
  • RNA, Messenger / analysis*
  • Reference Standards
  • Templates, Genetic

Substances

  • DNA, Complementary
  • Interleukin-8
  • RNA, Messenger
  • Glyceraldehyde-3-Phosphate Dehydrogenases