Division of Hematology/Oncology, Vanderbilt University Medical Center, Nashville, Tennessee 37232-6307, USA.
Stem Cells. 2013 May;31(5):882-94. doi: 10.1002/stem.1345.
LIM domain only 2 (Lmo2) is frequently deregulated in sporadic and gene therapy-induced acute T-cell lymphoblastic leukemia (T-ALL) where its overexpression is an important initiating mutational event. In transgenic and retroviral mouse models, Lmo2 expression can be enforced in multiple hematopoietic lineages but leukemia only arises from T cells. These data suggest that Lmo2 confers clonal growth advantage in T-cell progenitors. We analyzed proliferation, differentiation, and cell death in CD2-Lmo2 transgenic thymic progenitor cells to understand the cellular effects of enforced Lmo2 expression. Most impressively, Lmo2 transgenic T-cell progenitor cells were blocked in differentiation, quiescent, and immortalized in vitro on OP9-DL1 stromal cells. These cellular effects were concordant with a transcriptional signature in Lmo2 transgenic T-cell progenitor cells that is also present in hematopoietic stem cells (HSCs) and early T-cell precursor ALL. These results are significant in light of the crucial role of Lmo2 in the maintenance of the HSC. The cellular effects and transcriptional effects have implications for LMO2-dependent leukemogenesis and the treatment of LMO2-induced T-ALL.
LIM 结构域只有 2(Lmo2)在散发和基因治疗诱导的急性 T 细胞淋巴细胞白血病(T-ALL)中经常失调,其过表达是一个重要的起始突变事件。在转基因和逆转录病毒小鼠模型中,Lmo2 的表达可以在多种造血谱系中被强制表达,但只有 T 细胞才会发生白血病。这些数据表明,Lmo2 在 T 细胞祖细胞中赋予克隆生长优势。我们分析了 CD2-Lmo2 转基因胸腺祖细胞的增殖、分化和细胞死亡,以了解强制表达 Lmo2 的细胞效应。最令人印象深刻的是,Lmo2 转基因 T 细胞祖细胞在体外 OP9-DL1 基质细胞上分化、静止和永生化被阻断。这些细胞效应与 Lmo2 转基因 T 细胞祖细胞中的转录特征一致,该特征也存在于造血干细胞(HSCs)和早期 T 细胞前体 ALL 中。鉴于 Lmo2 在维持 HSC 中的关键作用,这些结果具有重要意义。这些细胞效应和转录效应对 LMO2 依赖性白血病发生和 LMO2 诱导的 T-ALL 的治疗具有重要意义。