Herman B. Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, Indiana; Department of Pediatrics and Neonatal-Perinatal Medicine, Indiana University School of Medicine, Indianapolis, Indiana.
Herman B. Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, Indiana; Department of Pediatrics and Neonatal-Perinatal Medicine, Indiana University School of Medicine, Indianapolis, Indiana; Department of Biochemistry and Molecular Biology, Indiana University School of Medicine, Indianapolis, Indiana.
Am J Pathol. 2014 Jan;184(1):79-85. doi: 10.1016/j.ajpath.2013.09.022. Epub 2013 Nov 7.
Neurofibromatosis type 1 (NF1) results from mutations in the NF1 tumor-suppressor gene, which encodes neurofibromin, a negative regulator of diverse Ras signaling cascades. Arterial stenosis is a nonneoplastic manifestation of NF1 that predisposes some patients to debilitating morbidity and sudden death. Recent murine studies demonstrate that Nf1 heterozygosity (Nf1(+/-)) in monocytes/macrophages significantly enhances intimal proliferation after arterial injury. However, the downstream Ras effector pathway responsible for this phenotype is unknown. Based on in vitro assays demonstrating enhanced extracellular signal-related kinase (Erk) signaling in Nf1(+/-) macrophages and vascular smooth muscle cells and in vivo evidence of Erk amplification without alteration of phosphatidylinositol 3-kinase signaling in Nf1(+/-) neointimas, we tested the hypothesis that Ras-Erk signaling regulates intimal proliferation in a murine model of NF1 arterial stenosis. By using a well-established in vivo model of inflammatory cell migration and standard cell culture, neurofibromin-deficient macrophages demonstrate enhanced sensitivity to growth factor stimulation in vivo and in vitro, which is significantly diminished in the presence of PD0325901, a specific inhibitor of Ras-Erk signaling in phase 2 clinical trials for cancer. After carotid artery injury, Nf1(+/-) mice demonstrated increased intimal proliferation compared with wild-type mice. Daily administration of PD0325901 significantly reduced Nf1(+/-) neointima formation to levels of wild-type mice. These studies identify the Ras-Erk pathway in neurofibromin-deficient macrophages as the aberrant pathway responsible for enhanced neointima formation.
神经纤维瘤病 1 型(NF1)是由 NF1 肿瘤抑制基因的突变引起的,该基因编码神经纤维瘤蛋白,是多种 Ras 信号级联的负调节剂。动脉狭窄是 NF1 的一种非肿瘤表现,使一些患者易患致残性发病率和猝死。最近的小鼠研究表明,单核细胞/巨噬细胞中的 Nf1 杂合性(Nf1(+/-))显著增强动脉损伤后的内膜增殖。然而,负责这种表型的下游 Ras 效应物途径尚不清楚。基于体外实验证明 Nf1(+/-)巨噬细胞和血管平滑肌细胞中细胞外信号相关激酶(Erk)信号增强,以及 Nf1(+/-)新生内膜中 Erk 扩增而磷脂酰肌醇 3-激酶信号无改变的体内证据,我们测试了 Ras-Erk 信号调节 NF1 动脉狭窄小鼠模型中内膜增殖的假设。通过使用成熟的炎症细胞迁移体内模型和标准细胞培养,神经纤维瘤蛋白缺陷型巨噬细胞在体内和体外表现出对生长因子刺激的敏感性增强,而在 Ras-Erk 信号特异性抑制剂 PD0325901 的存在下,这种敏感性显著降低,PD0325901 正在进行癌症的 2 期临床试验。颈动脉损伤后,Nf1(+/-)小鼠的内膜增殖明显高于野生型小鼠。每天给予 PD0325901 可显著减少 Nf1(+/-)新生内膜形成,使其达到野生型小鼠的水平。这些研究确定了神经纤维瘤蛋白缺陷型巨噬细胞中的 Ras-Erk 途径是导致新生内膜形成增强的异常途径。