Mayasich Sally A, Korte Joseph J, Denny Jeffrey S, Hartig Phillip C, Olker Jennifer H, DeGoey Philip, O'Flanagan Joseph, Degitz Sigmund J, Hornung Michael W
Oak Ridge Institute for Science and Education, Oak Ridge, TN, USA; Great Lakes Toxicology and Ecology Division, Center for Computational Toxicology and Ecology, Office of Research and Development, U.S. Environmental Protection Agency, Duluth, MN, USA.
Great Lakes Toxicology and Ecology Division, Center for Computational Toxicology and Ecology, Office of Research and Development, U.S. Environmental Protection Agency, Duluth, MN, USA.
Toxicol In Vitro. 2021 Jun;73:105141. doi: 10.1016/j.tiv.2021.105141. Epub 2021 Mar 11.
Deiodinase enzymes are critical for tissue-specific and temporal control of activation or inactivation of thyroid hormones during vertebrate development, including amphibian metamorphosis. We previously screened ToxCast chemicals for inhibitory activity toward human recombinant Type 3 iodothyronine deiodinase enzyme (hDIO3) and subsequently produced Xenopus laevis recombinant dio3 enzyme (Xldio3) with the goals to identify specific chemical inhibitors of Xldio3, to evaluate cross-species sensitivity and explore whether the human assay results are predictive of the amphibian. We identified a subset of 356 chemicals screened against hDIO3 to test against Xldio3, initially at a single concentration (200 μM), and further tested 79 in concentration-response mode. Most chemicals had IC values lower for hDIO3 than for Xldio3 and many had steep Hill slopes (a potential indication of non-specific inhibition). However, eight of the most potent chemicals are likely specific inhibitors, with IC values of 14 μM or less, Hill slopes near -1 and curves not significantly different between species likely due to conservation of catalytically active amino acids. Controlling for assay conditions, human in vitro screening results can be predictive of activity in the amphibian assay. This study lays the groundwork for future studies using recombinant non-mammalian proteins to test cross-species sensitivity to chemicals. DISCLAIMER: The views expressed in this paper are those of the authors and do not necessarily reflect the views or policies of the U.S. Environmental Protection Agency. Mention of trade names or commercial products does not constitute endorsement or recommendation for use.
脱碘酶对于脊椎动物发育过程中甲状腺激素激活或失活的组织特异性和时间控制至关重要,包括两栖动物变态发育。我们之前筛选了ToxCast化学物质对人重组3型碘甲状腺原氨酸脱碘酶(hDIO3)的抑制活性,随后制备了非洲爪蟾重组dio3酶(Xldio3),目的是鉴定Xldio3的特异性化学抑制剂,评估跨物种敏感性,并探讨人体试验结果是否能预测两栖动物的情况。我们从针对hDIO3筛选的356种化学物质中挑选出一部分来测试对Xldio3的作用,最初在单一浓度(200 μM)下进行测试,然后对79种进行浓度响应模式测试。大多数化学物质对hDIO3的IC值低于对Xldio3的IC值,且许多具有陡峭的希尔斜率(这可能是非特异性抑制的一个迹象)。然而,八种最有效的化学物质可能是特异性抑制剂,IC值为14 μM或更低,希尔斜率接近 -1,不同物种间曲线无显著差异,这可能是由于催化活性氨基酸保守所致。在控制试验条件的情况下,人体体外筛选结果可预测两栖动物试验中的活性。本研究为未来使用重组非哺乳动物蛋白测试化学物质跨物种敏感性的研究奠定了基础。免责声明:本文所表达的观点仅为作者观点,不一定反映美国环境保护局的观点或政策。提及商品名或商业产品并不构成对其使用的认可或推荐。