Trowbridge Jennifer J, Scott Matthew P, Bhatia Mickie
Department of Microbiology and Immunology, University of Western Ontario, 1151 Richmond Street, Suite 2, London, ON, Canada N6A 5B8.
Proc Natl Acad Sci U S A. 2006 Sep 19;103(38):14134-9. doi: 10.1073/pnas.0604568103. Epub 2006 Sep 12.
The signals that control the regenerative ability of hematopoietic stem cells (HSCs) in response to damage are unknown. Here, we demonstrate that downstream activation of the Hedgehog (Hh) signaling pathway induces cycling and expansion of primitive bone marrow hematopoietic cells under homeostatic conditions and during acute regeneration. However, this effect is at the expense of HSC function, because continued Hh activation during regeneration represses expression of specific cell cycle regulators, leading to HSC exhaustion. In vivo treatment with an inhibitor of the Hh pathway rescues these transcriptional and functional defects in HSCs. Our study establishes Hh signaling as a regulator of the HSC cell cycle machinery that balances hematopoietic homeostasis and regeneration in vivo.
控制造血干细胞(HSC)在损伤后再生能力的信号尚不清楚。在此,我们证明,在稳态条件下和急性再生过程中,Hedgehog(Hh)信号通路的下游激活会诱导原始骨髓造血细胞的循环和扩增。然而,这种效应是以牺牲HSC功能为代价的,因为再生过程中持续的Hh激活会抑制特定细胞周期调节因子的表达,导致HSC耗竭。用Hh通路抑制剂进行体内治疗可挽救HSC中的这些转录和功能缺陷。我们的研究将Hh信号确立为HSC细胞周期机制的调节因子,其在体内平衡造血稳态和再生。