Ksionda O, Melton A A, Bache J, Tenhagen M, Bakker J, Harvey R, Winter S S, Rubio I, Roose J P
Department of Anatomy, Roose University of California, San Francisco, San Francisco, CA, USA.
Department of Pediatrics, University of California, San Francisco, San Francisco, CA, USA.
Oncogene. 2016 Jul 14;35(28):3658-68. doi: 10.1038/onc.2015.431. Epub 2015 Nov 9.
Ras GTPases are activated by RasGEFs and inactivated by RasGAPs, which stimulate the hydrolysis of RasGTP to inactive RasGDP. GTPase-impairing somatic mutations in RAS genes, such as KRAS(G12D), are among the most common oncogenic events in metastatic cancer. A different type of cancer Ras signal, driven by overexpression of the RasGEF RasGRP1 (Ras guanine nucleotide-releasing protein 1), was recently implicated in pediatric T-cell acute lymphoblastic leukemia (T-ALL) patients and murine models, in which RasGRP1 T-ALLs expand in response to treatment with interleukins (ILs) 2, 7 and 9. Here, we demonstrate that IL-2/7/9 stimulation activates Erk and Akt pathways downstream of Ras in RasGRP1 T-ALL but not in normal thymocytes. In normal lymphocytes, RasGRP1 is recruited to the membrane by diacylglycerol (DAG) in a phospholipase C-γ (PLCγ)-dependent manner. Surprisingly, we find that leukemic RasGRP1-triggered Ras-Akt signals do not depend on acute activation of PLCγ to generate DAG but rely on baseline DAG levels instead. In agreement, using three distinct assays that measure different aspects of the RasGTP/GDP cycle, we established that overexpression of RasGRP1 in T-ALLs results in a constitutively high GTP-loading rate of Ras, which is constantly counterbalanced by hydrolysis of RasGTP. KRAS(G12D) T-ALLs do not show constitutive GTP loading of Ras. Thus, we reveal an entirely novel type of leukemogenic Ras signals that is based on a RasGRP1-driven increased in flux through the RasGTP/GDP cycle, which is mechanistically very different from KRAS(G12D) signals. Our studies highlight the dynamic balance between RasGEF and RasGAP in these T-ALLs and put forth a new model in which IL-2/7/9 decrease RasGAP activity.
Ras GTP酶由Ras鸟嘌呤核苷酸交换因子(RasGEFs)激活,并由Ras GTP酶激活蛋白(RasGAPs)使其失活,后者可刺激RasGTP水解为无活性的RasGDP。RAS基因中影响GTP酶功能的体细胞突变,如KRAS(G12D),是转移性癌症中最常见的致癌事件之一。最近,由RasGEF RasGRP1(Ras鸟嘌呤核苷酸释放蛋白1)过表达驱动的另一种癌症Ras信号,在儿科T细胞急性淋巴细胞白血病(T-ALL)患者和小鼠模型中被发现,其中RasGRP1 T-ALLs在白介素(ILs)2、7和9的治疗下会扩增。在这里,我们证明IL-2/7/9刺激在RasGRP1 T-ALL中激活Ras下游的Erk和Akt通路,但在正常胸腺细胞中则不会。在正常淋巴细胞中,RasGRP1通过磷脂酶C-γ(PLCγ)依赖性方式被二酰基甘油(DAG)招募到细胞膜上。令人惊讶的是,我们发现白血病性RasGRP1触发的Ras-Akt信号不依赖于PLCγ的急性激活来生成DAG,而是依赖于基线DAG水平。与此一致,我们使用三种不同的检测方法来测量RasGTP/GDP循环的不同方面,确定了RasGRP1在T-ALLs中的过表达导致Ras的组成性高GTP负载率,而RasGTP的水解不断对其进行平衡。KRAS(G12D)T-ALLs未显示Ras的组成性GTP负载。因此,我们揭示了一种全新的致白血病Ras信号类型,它基于RasGRP1驱动的RasGTP/GDP循环通量增加,其机制与KRAS(G12D)信号非常不同。我们的研究强调了这些T-ALLs中RasGEF和RasGAP之间的动态平衡,并提出了一个新模型,其中IL-2/7/9会降低RasGAP活性。