Tritium contamination of hematopoietic stem cells alters long-term hematopoietic reconstitution

Int J Radiat Biol. 2011 Jun;87(6):556-70. doi: 10.3109/09553002.2011.565399. Epub 2011 Apr 7.

Abstract

Purpose: In vivo effects of tritium contamination are poorly documented. Here, we study the effects of tritiated Thymidine ([(3)H] Thymidine) or tritiated water (HTO) contamination on the biological properties of hematopoietic stem cells (HSC).

Materials and methods: Mouse HSC were contaminated with concentrations of [(3)H] Thymidine ranging from 0.37-37.03 kBq/ml or of HTO ranging from 5-50 kBq/ml. The biological properties of contaminated HSC were studied in vitro after HTO contamination and in vitro and in vivo after [(3)H] Thymidine contamination.

Results: Proliferation, viability and double-strand breaks were dependent on [(3)H] Thymidine or HTO concentrations used for contamination but in vitro myeloid differentiation of HSC was not affected by [(3)H] Thymidine contamination. [(3)H] Thymidine contaminated HSC showed a compromised long-term capacity of hematopoietic reconstitution and competition experiments showed an up to two-fold decreased capacity of contaminated HSC to reconstitute hematopoiesis. These defects were not due to impaired homing in bone marrow but to an initial decreased proliferation rate of HSC.

Conclusion: These results indicate that contaminations of HSC with doses of tritium that do not result in cell death, induce short-term effects on proliferation and cell cycle and long-term effects on hematopoietic reconstitution capacity of contaminated HSC.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis
  • Autoradiography / methods
  • Bone Marrow / metabolism
  • Bone Marrow Transplantation
  • Cell Cycle
  • Cell Proliferation
  • Flow Cytometry / methods
  • Hematopoiesis / radiation effects*
  • Hematopoietic Stem Cells / radiation effects*
  • Histones / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Stem Cells
  • Tritium / pharmacology*

Substances

  • H2AX protein, human
  • Histones
  • Tritium