Deletion of Puma protects hematopoietic stem cells and confers long-term survival in response to high-dose gamma-irradiation

Blood. 2010 Apr 29;115(17):3472-80. doi: 10.1182/blood-2009-10-248278. Epub 2010 Feb 22.


Molecular paradigms underlying the death of hematopoietic stem cells (HSCs) induced by ionizing radiation are poorly defined. We have examined the role of Puma (p53 up-regulated mediator of apoptosis) in apoptosis of HSCs after radiation injury. In the absence of Puma, HSCs were highly resistant to gamma-radiation in a cell autonomous manner. As a result, Puma-null mice or the wild-type mice reconstituted with Puma-null bone marrow cells were strikingly able to survive for a long term after high-dose gamma-radiation that normally would pose 100% lethality on wild-type animals. Interestingly, there was no increase of malignancy in the exposed animals. Such profound beneficial effects of Puma deficiency were likely associated with better maintained quiescence and more efficient DNA repair in the stem cells. This study demonstrates that Puma is a unique mediator in radiation-induced death of HSCs. Puma may be a potential target for developing an effective treatment aimed to protect HSCs from lethal radiation.

MeSH terms

  • Animals
  • Apoptosis / genetics*
  • Apoptosis / radiation effects*
  • Apoptosis Regulatory Proteins*
  • Cell Survival / genetics
  • Cell Survival / radiation effects
  • DNA Repair / genetics*
  • DNA Repair / radiation effects*
  • Gamma Rays / adverse effects*
  • Gene Deletion
  • Hematopoietic Stem Cells / metabolism*
  • Mice
  • Mice, Transgenic
  • Tumor Suppressor Proteins*


  • Apoptosis Regulatory Proteins
  • PUMA protein, mouse
  • Tumor Suppressor Proteins