Quantitative method to determine mRNA levels by reverse transcriptase-polymerase chain reaction from leukocyte subsets purified by fluorescence-activated cell sorting: application to peripheral cannabinoid receptors

Cytometry. 1999 Mar 1;35(3):227-34. doi: 10.1002/(sici)1097-0320(19990301)35:3<227::aid-cyto5>3.0.co;2-4.

Abstract

Background: While cytometry is widely used in the detection of cell proteins, its application to quantitative evaluation remains problematic when target proteins or receptors are weakly expressed in cells. Reverse transcriptase-polymerase chain reaction (RT-PCR) is a technique whose sensitivity and specificity make it appropriate for analyzing nucleic acids and thus genes expressed in cells. Combining these two techniques, we developed a method to quantify the transcript expression of the peripheral cannabinoid receptor (CB2-r) in peripheral blood lymphocyte subpopulations and in tonsillar B-cell subpopulations.

Methods: This strategy first involves quantitative RT-PCR performed kinetically, followed by enzyme detection of PCR products using an oligonucleotide probe sandwich-hybridization assay onto microplates.

Results: B cells exhibit CB2-receptor mRNA levels 10 times higher than those of other lymphocyte subsets. Using this technique, we observed a modulation of CB2-r mRNA level following tonsillar B-cell differentiation. Lastly, this new technology was validated by comparing the mRNA levels of CB2-r with the expression of CB2-r proteins assayed by flow cytometry, using specific CB2-r antibody labelling.

Conclusions: This method allows precise measurement of the mRNA of CB2-r performed on cell numbers as low as 10(5) after sorting. Its performance, high accuracy, reproducibility, and reliability make it a valuable tool for assaying proteins weakly expressed in cells.

Publication types

  • Comparative Study

MeSH terms

  • B-Lymphocytes / metabolism
  • Cell Differentiation
  • Cell Separation
  • DNA, Complementary / metabolism
  • Flow Cytometry / methods*
  • Leukocytes / metabolism*
  • Leukocytes, Mononuclear / metabolism
  • Poly A / metabolism
  • RNA, Messenger / analysis*
  • Receptors, Cannabinoid
  • Receptors, Drug / metabolism*
  • Reproducibility of Results
  • Reverse Transcriptase Polymerase Chain Reaction / methods*
  • Sensitivity and Specificity

Substances

  • DNA, Complementary
  • RNA, Messenger
  • Receptors, Cannabinoid
  • Receptors, Drug
  • Poly A