Feng Carl G, Weksberg David C, Taylor Gregory A, Sher Alan, Goodell Margaret A
Immunobiology Section, Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA.
Cell Stem Cell. 2008 Jan 10;2(1):83-9. doi: 10.1016/j.stem.2007.10.007.
Hematopoietic stem cells (HSCs) are self-renewing bone marrow cells that give rise to all blood lineages and retain a remarkable capacity to proliferate in response to insult. Although some controls on HSC activation are known, little is understood about how this process is linked to natural signals. We report that the interferon-inducible GTPase Lrg-47 (Irgm1), previously shown to play a critical role in host defense, inhibits baseline HSC proliferation and is required for a normal HSC response to chemical and infectious stimuli. Overproliferating Lrg-47(-/-) HSCs are severely impaired in functional repopulation assays, and when challenged with hematopoietic ablation by 5-fluorouracil or infection with Mycobacterium avium, Lrg-47(-/-) mice fail to achieve the expected expansion response in stem and progenitor cell populations. Our results establish a link between the response to infection and HSC activation and demonstrate a novel function for a member of the p47 GTPase family.
造血干细胞(HSCs)是能够自我更新的骨髓细胞,可分化为所有血细胞谱系,并在受到损伤时保持显著的增殖能力。尽管已知一些对造血干细胞激活的调控机制,但对于该过程如何与自然信号相联系却知之甚少。我们报告称,干扰素诱导型GTP酶Lrg-47(Irgm1),先前已证明其在宿主防御中起关键作用,可抑制造血干细胞的基础增殖,并且是造血干细胞对化学和感染性刺激产生正常反应所必需的。在功能重建试验中,过度增殖的Lrg-47(-/-)造血干细胞严重受损,当用5-氟尿嘧啶进行造血消融或感染鸟分枝杆菌时,Lrg-47(-/-)小鼠在干细胞和祖细胞群体中未能实现预期的扩增反应。我们的结果建立了感染反应与造血干细胞激活之间的联系,并证明了p47 GTP酶家族成员的一种新功能。