Meis1 preserves hematopoietic stem cells in mice by limiting oxidative stress

被引:83
作者
Unnisa, Zeenath [1 ]
Clark, Jason P. [1 ]
Roychoudhury, Jayeeta [1 ]
Thomas, Elizabeth [1 ]
Tessarollo, Lino [2 ]
Copeland, Neal G. [3 ]
Jenkins, Nancy A. [3 ]
Grimes, H. Leighton [1 ]
Kumar, Ashish R. [1 ]
机构
[1] Cincinnati Childrens Hosp Med Ctr, Canc & Blood Dis Inst, Cincinnati, OH 45236 USA
[2] NCI, Ctr Canc Res, Frederick, MD 21701 USA
[3] Methodist Hosp, Res Inst, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
ACUTE MYELOID-LEUKEMIA; DEFINITIVE HEMATOPOIESIS; IN-VIVO; HYPOXIA; EXPRESSION; GENES; QUIESCENCE; HIF-1-ALPHA; HOMEOSTASIS; MUTATIONS;
D O I
10.1182/blood-2012-06-435800
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The transcription factor Meis1 is expressed preferentially in hematopoietic stem cells (HSCs) and overexpressed in certain leukemias. However, the functions of Meis1 in hematopoiesis remain largely unknown. In the present study, we found that Meis1 is required for the maintenance of hematopoiesis under stress and over the long term, whereas steady-state hematopoiesis was sustained in the absence of Meis1 in inducible knock-out mice. BM cells of Meis1-deficient mice showed reduced colony formation and contained significantly fewer numbers of long-term HSCs, which exhibited loss of quiescence. Further, we found that Meis1 deletion led to the accumulation of reactive oxygen species in HSCs and decreased expression of genes implicated in hypoxia response. Finally, reactive oxygen species scavenging by N-acetyl cysteine or stabilization of hypoxia signaling by knockdown of the von-Hippel-Lindau (VHL) protein led to reversal of the effects of Meis1 deletion. The results of the present study demonstrate that Meis1 protects and preserves HSCs by restricting oxidative metabolism. (Blood. 2012; 120(25): 4973-4981)
引用
收藏
页码:4973 / 4981
页数:9
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