Transcription factor Gfi1 regulates self-renewal and engraftment of hematopoietic stem cells

被引:239
作者
Zeng, H [1 ]
Yücel, R [1 ]
Kosan, C [1 ]
Klein-Hitpass, L [1 ]
Möröy, T [1 ]
机构
[1] Univ Klinikum Essen, IFZ, Inst Zellbiol Tumorforsch, D-45122 Essen, Germany
关键词
cell cycle; proliferation; self-renewal; stem cells; zinc-finger transcription factor;
D O I
10.1038/sj.emboj.7600419
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The generation of all blood cells depends on the ability of hematopoietic stem cells (HSCs) for self-renewal and multilineage differentiation. We show here that the transcription factor Gfi1 is expressed in HSCs and in more mature cells such as common lymphoid progenitors (CLPs) and granulo/monocytic progenitors, but is absent in common myeloid progenitors and megakaryocyte/erythroid progenitors. When Gfi1 is deleted in mice, HSC frequencies are significantly reduced and CLPs all but disappear from the bone marrow. This specific requirement of Gfi1 for the maintenance of HSC numbers is cell autonomous. Transplantation of Gfi1-deficient bone marrow results in a compromised radioprotection and lower numbers of colony forming units in the spleen of wild-type recipients. Strikingly, Gfi1(-/-) bone marrow cells are severely impaired in competitive long-term reconstituting abilities after transplantation and show a surprisingly high proportion of actively cycling HSCs, suggesting that Gfi1 restrains proliferation of HSCs and thereby regulates their self-renewal and long-term engraftment abilities.
引用
收藏
页码:4116 / 4125
页数:10
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