Hubrecht Institute, Royal Netherlands Academy of Arts and Sciences and University Medical Center Utrecht, Utrecht, The Netherlands.
Dis Model Mech. 2010 May-Jun;3(5-6):343-53. doi: 10.1242/dmm.004036. Epub 2010 Mar 24.
Biallelic inactivation of the von Hippel-Lindau (VHL) tumor suppressor gene predisposes human patients to the development of highly vascularized neoplasms in multiple organ systems. We show that zebrafish vhl mutants display a marked increase in blood vessel formation throughout the embryo, starting at 2 days post-fertilization. The most severe neovascularization is observed in distinct areas that overlap with high vegfa mRNA expression, including the vhl mutant brain and eye. Real-time quantitative PCR revealed increased expression of the duplicated VEGFA orthologs vegfaa and vegfab, and of vegfb and its receptors flt1, kdr and kdr-like, indicating increased vascular endothelial growth factor (Vegf) signaling in vhl mutants. Similar to VHL-associated retinal neoplasms, diabetic retinopathy and age-related macular degeneration, we show, by tetramethyl rhodamine-dextran angiography, that vascular abnormalities in the vhl(-/-) retina lead to vascular leakage, severe macular edema and retinal detachment. Significantly, vessels in the brain and eye express cxcr4a, a marker gene expressed by tumor and vascular cells in VHL-associated hemangioblastomas and renal cell carcinomas. VEGF receptor (VEGFR) tyrosine kinase inhibition (through exposure to sunitinib and 676475) blocked vhl(-/-)-induced angiogenesis in all affected tissues, demonstrating that Vegfaa, Vegfab and Vegfb are key effectors of the vhl(-/-) angiogenic phenotype through Flt1, Kdr and Kdr-like signaling. Since we show that the vhl(-/-) angiogenic phenotype shares distinct characteristics with VHL-associated vascular neoplasms, zebrafish vhl mutants provide a valuable in vivo vertebrate model to elucidate underlying mechanisms contributing to the development of these lesions. Furthermore, vhl mutant zebrafish embryos carrying blood vessel-specific transgenes represent a unique and clinically relevant model for tissue-specific, hypoxia-induced pathological angiogenesis and vascular retinopathies. Importantly, they will allow for a cost-effective, non-invasive and efficient way to screen for novel pharmacological agents and combinatorial treatments.
双侧失活 von Hippel-Lindau(VHL)肿瘤抑制基因可使人类患者易患多种器官系统中高度血管化的肿瘤。我们发现,斑马鱼 vhl 突变体在受精后 2 天开始,胚胎内的血管生成明显增加。在与高 vegfa mRNA 表达重叠的特定区域观察到最严重的新生血管化,包括 vhl 突变体的大脑和眼睛。实时定量 PCR 显示,duplicated VEGFA 同源物 vegfaa 和 vegfab,以及 vegfb 和其受体 flt1、kdr 和 kdr-like 的表达增加,表明 vhl 突变体中血管内皮生长因子(VEGF)信号增加。与 VHL 相关的视网膜肿瘤、糖尿病性视网膜病变和年龄相关性黄斑变性相似,我们通过四甲基罗丹明-葡聚糖血管造影显示,vhl(-/-)视网膜中的血管异常导致血管渗漏、严重的黄斑水肿和视网膜脱离。重要的是,大脑和眼睛中的血管表达 cxcr4a,这是 VHL 相关血管母细胞瘤和肾细胞癌中肿瘤和血管细胞表达的标记基因。VEGF 受体(VEGFR)酪氨酸激酶抑制(通过暴露于舒尼替尼和 676475)阻断了所有受影响组织中 vhl(-/-)诱导的血管生成,表明 Vegfaa、Vegfab 和 Vegfb 通过 Flt1、Kdr 和 Kdr-like 信号是 vhl(-/-)血管生成表型的关键效应物。由于我们表明 vhl(-/-)血管生成表型与 VHL 相关的血管肿瘤具有明显的特征,因此斑马鱼 vhl 突变体为阐明导致这些病变发展的潜在机制提供了有价值的体内脊椎动物模型。此外,携带血管特异性转基因的 vhl(-/-)斑马鱼胚胎代表了一种独特且具有临床相关性的组织特异性、缺氧诱导的病理性血管生成和血管性视网膜病变模型。重要的是,它们将为新型药理学制剂和联合治疗的筛选提供一种具有成本效益、非侵入性和高效的方法。