Mutation frequency in human blood cells increases with age

Mutat Res. 1995 Oct;338(1-6):141-9. doi: 10.1016/0921-8734(95)00019-3.


Using either the colony formation assay or flow cytometry, it is feasible to measure the frequency of rare mutant lymphocytes or erythrocytes in human peripheral blood. Accordingly, we have investigated the mutant cell frequencies of the hypoxanthine-guanine phosphoribosyltransferase and T-cell receptor genes in T lymphocytes and of the glycophorin A gene in erythrocytes of several hundred persons aged 0-96 years. The mutant frequency of every one of these genes increased significantly with age. A simple accumulation of mutations in hematopoietic stem cells over time may explain the age-dependent increase in the frequency of glycophorin A mutants. In contrast, a balance between mutant cell generation and loss should be taken into account for the mechanism of the increase of T-cell mutations.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Child
  • Child, Preschool
  • Chromosome Aberrations / genetics
  • Clone Cells
  • DNA Replication / genetics
  • Erythrocytes / chemistry*
  • Female
  • Glycophorins / genetics*
  • Hematopoietic Stem Cells / chemistry
  • Humans
  • Hypoxanthine Phosphoribosyltransferase / blood
  • Hypoxanthine Phosphoribosyltransferase / genetics*
  • Infant
  • Infant, Newborn
  • Male
  • Middle Aged
  • Mutation / genetics*
  • Receptors, Antigen, T-Cell / genetics*
  • T-Lymphocytes / chemistry*


  • Glycophorins
  • Receptors, Antigen, T-Cell
  • Hypoxanthine Phosphoribosyltransferase