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Blood, 1 January 2006, Vol. 107, No. 1, pp. 358-366.
Prepublished online as a Blood First Edition Paper on September 8, 2005; DOI 10.1182/blood-2005-04-1418.
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Submitted April 7, 2005
Accepted August 23, 2005
Total body irradiation selectively induces murine hematopoietic stem cell senescence
Yong Wang, Bradley A Schulte, Amanda C LaRue, Makio Ogawa, and Daohong Zhou*
Department of Pathology & Laboratory Medicine, Medical University of South Carolina, Charleston, SC, USA
Department of Medicine, Medical University of South Carolina, Charleston, SC, USA; Department of Veterans Affairs Medical Center, Charleston, SC, USA
* Corresponding author; email: zhoud{at}musc.edu.
Exposure to ionizing radiation (IR) and certain chemotherapeutic agents not only causes acute bone marrow (BM) suppression but also leads to long-term residual hematopoietic injury. This later effect has been attributed to the damage to hematopoietic stem cell (HSC) self-renewal. Using a mouse model, we investigated whether IR induces senescence in HSCs, as induction of HSC senescence can lead to the defect in HSC self-renewal. It was found that exposure of C57BL/6 mice to a sublethal dose (6.5 Gy) of total body irradiation (TBI) resulted in a sustained quantitative and qualitative reduction of LKS+ HSCs. In addition, LKS+ HSCs from irradiated mice exhibited an increased expression of the two commonly used biomarkers of cellular senescence, p16Ink4a and SA- -gal. In contrast, no such changes were observed in irradiated LKS- hematopoietic progenitor cells. These results provide the first direct evidence demonstrating that IR exposure can selectively induce HSC senescence. Interestingly, the induction of HSC senescence was associated with a prolonged elevation of p21Cip1/Waf1, p19Arf and p16Ink4a mRNA expression, while the expression of p27Kip1 and p18Ink4c mRNA was not increased following TBI. This suggests that p21Cip1/Waf1, p19Arf and p16Ink4a may play an important role in IR-induced senescence in HSCs.

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