Wu Qiong, Yu Chunjie, Yu Fang, Guo Yiran, Sheng Yue, Li Liping, Li Yafang, Zhang Yutao, Hu Chao, Wang Jue, He Tong-Chuan, Huang Yong, Ni Hongyu, Huo Zhiguang, Wu Wenshu, Wang Gang Greg, Lyu Jianxin, Qian Zhijian
Zhejiang Provincial Key Laboratory of Medical Genetics, Key Laboratory of Laboratory Medicine, Ministry of Education, School of Laboratory Medicine and Life Sciences, Wenzhou Medical University, Wenzhou, Zhejiang, China.
Department of Medicine and Department of Biochemistry and Molecular Biology, UF Health Cancer Center, University of Florida, Gainesville, Florida, USA.
J Clin Invest. 2024 Dec 16;134(24):e173403. doi: 10.1172/JCI173403.
Ecotropic viral integration site 1 (EVI1/MECOM) is frequently upregulated in myeloid malignancies. Here, we present an Evi1-transgenic mouse model with inducible expression in hematopoietic stem/progenitor cells (HSPCs). Upon induction of Evi1 expression, mice displayed anemia, thrombocytopenia, lymphopenia, and erythroid and megakaryocyte dysplasia with a significant expansion of committed myeloid progenitor cells, resembling human myelodysplastic syndrome/myeloproliferative neoplasm-like (MDS/MPN-like) disease. Evi1 overexpression prompted HSPCs to exit quiescence and accelerated their proliferation, leading to expansion of committed myeloid progenitors while inhibiting lymphopoiesis. Analysis of global gene expression and Evi1 binding site profiling in HSPCs revealed that Evi1 directly upregulated lysine demethylase 6b (Kdm6b). Subsequently, Kdm6b-mediated H3K27me3 demethylation resulted in activation of various genes, including Laptm4b. Interestingly, KDM6B and LAPTM4B are positively correlated with EVI1 expression in patients with MDS. The EVI1/KDM6B/H3K27me3/LAPTM4B signaling pathway was also identified in EVI1hi human leukemia cell lines. We found that hyperactivation of the LAPTM4B-driven mTOR pathway was crucial for the growth of EVI1hi leukemia cells. Knockdown of Laptm4b partially rescued Evi1-induced abnormal hematopoiesis in vivo. Thus, our study establishes a mouse model to investigate EVI1hi myeloid malignancies, demonstrating the significance of the EVI1-mediated KDM6B/H3K27me3/LAPTM4B signaling axis in their maintenance.
嗜亲性病毒整合位点1(EVI1/MECOM)在髓系恶性肿瘤中经常上调。在此,我们展示了一种在造血干/祖细胞(HSPCs)中可诱导表达的Evi1转基因小鼠模型。在诱导Evi1表达后,小鼠出现贫血、血小板减少、淋巴细胞减少以及红系和巨核细胞发育异常,伴有定向髓系祖细胞的显著扩增,类似于人类骨髓增生异常综合征/骨髓增殖性肿瘤样(MDS/MPN样)疾病。Evi1过表达促使HSPCs退出静止状态并加速其增殖,导致定向髓系祖细胞扩增,同时抑制淋巴细胞生成。对HSPCs的全基因组基因表达分析和Evi1结合位点图谱分析表明,Evi1直接上调赖氨酸去甲基化酶6b(Kdm6b)。随后,Kdm6b介导的H3K27me3去甲基化导致包括Laptm4b在内的多种基因激活。有趣的是,在MDS患者中,KDM6B和LAPTM4B与EVI1表达呈正相关。在EVI1高表达的人类白血病细胞系中也鉴定出了EVI1/KDM6B/H3K27me3/LAPTM4B信号通路。我们发现,LAPTM4B驱动的mTOR通路的过度激活对EVI1高表达白血病细胞的生长至关重要。敲低Laptm4b可部分挽救Evi1在体内诱导的异常造血。因此,我们的研究建立了一个用于研究EVI1高表达髓系恶性肿瘤的小鼠模型,证明了EVI1介导的KDM6B/H3K27me3/LAPTM4B信号轴在其维持中的重要性。