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Identification of vascular disruptor compounds by analysis in zebrafish embryos and mouse embryonic endothelial cells

机译:通过分析斑马鱼胚胎和小鼠胚胎内皮细胞中的血管破坏化合物

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摘要

To identify vascular disruptor compounds (VDCs), this study utilized an in vivo zebrafish embryo vascular model in conjunction with a mouse endothelial cell model to screen a subset of the U.S. Environmental Protection Agency (EPA) ToxCast Phase I chemical inventory. In zebrafish, 161 compounds were screened and 34 were identified by visual inspection as VDCs, of which 28 were confirmed as VDCs by quantitative image analysis. Testing of the zebrafish VDCs for their capacity to inhibit endothelial tube formation in the murine yolk-sac-derived endothelial cell line C166 identified 22 compounds that both disrupted zebrafish vascular development and murine endothelial in vitro tubulogenesis. Putative molecular targets for the VDCs were predicted using EPA’s Toxicological Prioritization Index tool and a VDC signature based on a proposed adverse outcome pathway for developmental vascular toxicity. In conclusion, our screening approach identified 22 novel VDCs, some of which were active at nanomolar concentrations
机译:为了识别血管分裂化合物(VDC),本研究利用体内斑马鱼胚胎血管模型与小鼠内皮细胞模型一起筛选了美国环境保护署(EPA)ToxCast I期化学药品清单的一部分。在斑马鱼中,筛选了161种化合物,目视检查鉴定出34种为VDC,其中28种通过定量图像分析确认为VDC。斑马鱼VDCs抑制鼠卵黄囊来源的内皮细胞系C166中抑制内皮管形成的能力的测试鉴定了22种化合物,它们既破坏了斑马鱼的血管发育,又破坏了鼠体外血管生成。 VDC的推测分子靶标是使用EPA的《毒理学优先指标》工具和VDC签名进行预测的,VDC签名基于拟议的发育性血管毒性不良反应途径。总之,我们的筛选方法确定了22种新型VDC,其中一些在纳摩尔浓度下具有活性

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