A novel method for isolation of human lung T cells from lung resection tissue reveals increased expression of GAPDH and CXCR6

J Immunol Methods. 2009 Mar 15;342(1-2):91-7. doi: 10.1016/j.jim.2008.12.001. Epub 2009 Jan 6.

Abstract

Lung T lymphocytes are important in pulmonary immunity and inflammation. It has been difficult to study these cells due to contamination with other cell types, mainly alveolar macrophages. We have developed a novel method for isolating lung T cells from lung resection tissue, using a combination of approaches. Firstly the lung tissue was finely chopped and filtered through a nylon mesh. Lymphocytic cells were enriched by Percoll density centrifugation and the T cells purified using human CD3 microbeads, resulting in 90.5%+/-1.9% (n=11) pure lymphocytes. The T cell yield from the crude cell preparation was 10.8+/-2.1% and viability, calculated using propidium iodide (PI) staining and trypan blue, was typically over 95%. The purification process did not affect expression of CD69 or CD103, nor was there a difference in the proportion of CD4 and CD8 cells between the starting population and the purified cells. Microarray analysis and real time RT-PCR revealed upregulation of GAPDH and CXCR6 of the lung T cells as compared to blood-derived T cells. This technique highly enriches lung T cells to allow detailed investigation of the biology of these cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • CD3 Complex
  • Cell Separation / methods*
  • Flow Cytometry
  • Glyceraldehyde-3-Phosphate Dehydrogenase (Phosphorylating) / metabolism*
  • Humans
  • Lung / cytology*
  • Lung / immunology
  • Microspheres
  • Oligonucleotide Array Sequence Analysis
  • Phenotype
  • Povidone
  • Receptors, CXCR6
  • Receptors, Chemokine / metabolism*
  • Receptors, Virus / metabolism*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Silicon Dioxide
  • T-Lymphocytes / cytology*
  • T-Lymphocytes / metabolism

Substances

  • CD3 Complex
  • CXCR6 protein, human
  • Receptors, CXCR6
  • Receptors, Chemokine
  • Receptors, Virus
  • Percoll
  • Silicon Dioxide
  • Glyceraldehyde-3-Phosphate Dehydrogenase (Phosphorylating)
  • Povidone