Department of Medicine, Division of Endocrinology, College of Physicians & Surgeons, Columbia University, New York, New York 10032, USA.
Department of Pathology and Cell Biology, College of Physicians & Surgeons, Columbia University, New York, New York 10032, USA.
Nature. 2014 Feb 13;506(7487):240-4. doi: 10.1038/nature12883. Epub 2014 Jan 15.
Cells of the osteoblast lineage affect the homing and the number of long-term repopulating haematopoietic stem cells, haematopoietic stem cell mobilization and lineage determination and B cell lymphopoiesis. Osteoblasts were recently implicated in pre-leukaemic conditions in mice. However, a single genetic change in osteoblasts that can induce leukaemogenesis has not been shown. Here we show that an activating mutation of β-catenin in mouse osteoblasts alters the differentiation potential of myeloid and lymphoid progenitors leading to development of acute myeloid leukaemia with common chromosomal aberrations and cell autonomous progression. Activated β-catenin stimulates expression of the Notch ligand jagged 1 in osteoblasts. Subsequent activation of Notch signalling in haematopoietic stem cell progenitors induces the malignant changes. Genetic or pharmacological inhibition of Notch signalling ameliorates acute myeloid leukaemia and demonstrates the pathogenic role of the Notch pathway. In 38% of patients with myelodysplastic syndromes or acute myeloid leukaemia, increased β-catenin signalling and nuclear accumulation was identified in osteoblasts and these patients showed increased Notch signalling in haematopoietic cells. These findings demonstrate that genetic alterations in osteoblasts can induce acute myeloid leukaemia, identify molecular signals leading to this transformation and suggest a potential novel pharmacotherapeutic approach to acute myeloid leukaemia.
成骨细胞系的细胞影响归巢和长期重编程造血干细胞、造血干细胞动员和谱系决定以及 B 细胞淋巴发生的数量。成骨细胞最近被牵连到小鼠的白血病前状态中。然而,尚未证明成骨细胞中的单个遗传改变可以诱导白血病发生。在这里,我们表明,小鼠成骨细胞中 β-连环蛋白的激活突变改变了髓系和淋巴系祖细胞的分化潜能,导致具有常见染色体异常和细胞自主进展的急性髓系白血病的发生。激活的 β-连环蛋白刺激成骨细胞中 Notch 配体 Jagged1 的表达。随后,造血干细胞祖细胞中 Notch 信号的激活诱导恶性变化。Notch 信号的遗传或药理学抑制可改善急性髓系白血病,并证明 Notch 通路的致病作用。在 38%的骨髓增生异常综合征或急性髓系白血病患者中,在成骨细胞中鉴定到增加的 β-连环蛋白信号和核积累,并且这些患者在造血细胞中显示出增加的 Notch 信号。这些发现表明,成骨细胞中的遗传改变可以诱导急性髓系白血病,确定导致这种转化的分子信号,并提示急性髓系白血病的一种潜在新的药物治疗方法。