Tal T L, McCollum C W, Harris P S, Olin J, Kleinstreuer N, Wood C E, Hans C, Shah S, Merchant F A, Bondesson M, Knudsen T B, Padilla S, Hemmer M J
Integrated Systems Toxicology Division, NHEERL, U.S. EPA, RTP, NC, United States.
Center for Nuclear Receptors and Cell Signaling, Department of Biology and Biochemistry, University of Houston, Houston, TX, United States.
Reprod Toxicol. 2014 Sep;48:51-61. doi: 10.1016/j.reprotox.2014.05.014. Epub 2014 Jun 4.
Proper formation of the vascular system is necessary for embryogenesis, and chemical disruption of vascular development may be a key event driving developmental toxicity. In order to test the effect of environmental chemicals on this critical process, we evaluated a quantitative assay in transgenic zebrafish using angiogenesis inhibitors that target VEGFR2 (PTK787) or EGFR (AG1478). Both PTK787 and AG1478 exposure impaired intersegmental vessel (ISV) sprouting, while AG1478 also produced caudal and pectoral fin defects at concentrations below those necessary to blunt ISV morphogenesis. The functional consequences of vessel toxicity during early development included decreased body length and survival in juvenile cohorts developmentally exposed to inhibitor concentrations sufficient to completely block ISV sprouting angiogenesis. These data show that concentration-dependent disruption of the presumed targets for these inhibitors produce adverse outcomes at advanced life stages.
血管系统的正常形成对于胚胎发育是必要的,而血管发育的化学性破坏可能是导致发育毒性的关键事件。为了测试环境化学物质对这一关键过程的影响,我们在转基因斑马鱼中使用靶向VEGFR2(PTK787)或EGFR(AG1478)的血管生成抑制剂评估了一种定量测定方法。暴露于PTK787和AG1478均会损害节间血管(ISV)的出芽,而AG1478在低于钝性ISV形态发生所需浓度时也会产生尾鳍和胸鳍缺陷。早期发育过程中血管毒性的功能后果包括,在发育过程中暴露于足以完全阻断ISV出芽血管生成的抑制剂浓度下的幼年鱼群中,体长和存活率降低。这些数据表明,这些抑制剂假定靶点的浓度依赖性破坏在生命后期会产生不良后果。