Santaguida Marianne, Schepers Koen, King Bryan, Sabnis Amit J, Forsberg E Camilla, Attema Joanne L, Braun Benjamin S, Passegué Emmanuelle
The Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research, Division of Hematology/Oncology, Department of Medicine, University of California, San Francisco, CA 94143, USA.
Cancer Cell. 2009 Apr 7;15(4):341-52. doi: 10.1016/j.ccr.2009.02.016.
Loss of the JunB/AP-1 transcription factor induces a myeloproliferative disease (MPD) arising from the hematopoietic stem cell (HSC) compartment. Here, we show that junB inactivation deregulates the cell-cycle machinery and increases the proliferation of long-term repopulating HSCs (LT-HSCs) without impairing their self-renewal or regenerative potential in vivo. We found that JunB loss destabilizes a complex network of genes and pathways that normally limit myeloid differentiation, leading to impaired responsiveness to both Notch and TGF-beta signaling due in part to transcriptional deregulation of the Hes1 gene. These results demonstrate that LT-HSC proliferation and differentiation are uncoupled from self-renewal and establish some of the mechanisms by which JunB normally limits the production of myeloid progenitors, hence preventing initiation of myeloid malignancies.
JunB/AP-1转录因子的缺失会引发一种起源于造血干细胞(HSC)区室的骨髓增殖性疾病(MPD)。在此,我们表明junB失活会失调细胞周期机制,并增加长期重建造血干细胞(LT-HSC)的增殖,而不会损害其在体内的自我更新或再生潜能。我们发现JunB缺失会破坏一个通常限制髓系分化的复杂基因和信号通路网络,导致对Notch和TGF-β信号的反应性受损,部分原因是Hes1基因的转录失调。这些结果表明,LT-HSC的增殖和分化与自我更新脱钩,并确立了JunB正常情况下限制髓系祖细胞产生从而预防髓系恶性肿瘤发生的一些机制。