High rate of mutation reporter gene inactivation during human T cell proliferation

Immunogenetics. 2007 Feb;59(2):135-43. doi: 10.1007/s00251-006-0180-8. Epub 2006 Dec 19.

Abstract

Caspase activation and degradation of deoxyribonucleic acid (DNA) damage response factors occur during in vitro T-cell proliferation, and an increased frequency of hypoxanthine-guanine phosphoribosyltransferase (HPRT)-negative variants have been reported in conditions associated with in vivo T-cell proliferation. We have applied two human somatic cell mutation reporter assays, for the HPRT and phosphatidylinositol glycan class A (PIG-A) genes, to human T cells activated in vitro with anti-CD3 and anti-CD28. We demonstrate proliferation throughout 6 weeks of cultivation, and find that the frequency of variant cells phenotypically negative for HPRT and PIG-A, respectively, increases from 10(-5) up to 10(-3) -10(-2). We also report preliminary evidence for low-density CpG methylation in the HPRT promoter suggesting that epigenetic modification may contribute to this markedly heightened rate of gene inactivation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Caspase 3 / metabolism
  • Cell Proliferation
  • CpG Islands
  • DNA Damage
  • DNA Primers / genetics
  • Genes, Reporter
  • Humans
  • Hypoxanthine Phosphoribosyltransferase / genetics
  • Immunogenetics
  • In Vitro Techniques
  • Lymphocyte Activation / genetics
  • Membrane Proteins / genetics
  • Mutation
  • T-Lymphocytes / cytology*
  • T-Lymphocytes / immunology*
  • T-Lymphocytes / metabolism

Substances

  • DNA Primers
  • Membrane Proteins
  • phosphatidylinositol glycan-class A protein
  • Hypoxanthine Phosphoribosyltransferase
  • Caspase 3