Science Inventory

Cross-species comparison of chemical inhibition of human and Xenopus iodotyrosine deiodinase

Citation:

Olker, J., J. Korte, Jonathan Haselman, M. Hornung, AND S. Degitz. Cross-species comparison of chemical inhibition of human and Xenopus iodotyrosine deiodinase. AQUATIC TOXICOLOGY. Elsevier Science Ltd, New York, NY, 249:106227, (2022). https://doi.org/10.1016/j.aquatox.2022.106227

Impact/Purpose:

Iodotyrosine deiodinase (IYD) has an important role in vertebrate thyroid hormone homeostasis through catalyzing iodide recycling and promoting retention of iodide in thyroid follicular cells. This manuscript describes a cross-species comparison in chemical inhibition of IYD enzyme using a newly developed amphibian IYD assay and the previously published human IYD assay. Included are the results from screening 154 chemicals from the ToxCast chemical library with both assays and comparison of potency and maximum inhibition produced. There was great similarity in inhibition produced by most chemicals, with differences primarily from greater maximum inhibitor or higher potency produced in the human IYD. These results suggest that the results from the human IYD assay would be predictive of chemical effects on amphibian IYD. This work supports the U.S. EPA Endocrine Disruptor Screening Program’s need for higher-throughput screening assays to address additional molecular initiating events, beyond those currently in the ToxCast suite of assays, with the potential to disrupt normal thyroid function.

Description:

The transition to include in vitro-based data in chemical hazard assessment has resulted in the development and implementation of screening assays to cover a diversity of biological pathways, including recently added assays to interrogate chemical disruption of proteins relevant to thyroid signaling pathways. Iodotyrosine deiodinase (IYD), the iodide recycling enzyme, is one such thyroid-relevant endpoint for which a human-based screening assay has recently been developed and used to screen large libraries of chemicals. Presented here is the development of an amphibian IYD inhibition assay and its implementation to conduct a cross-species comparison between chemical inhibition of mammalian and non-mammalian IYD enzyme activity. The successful development of an amphibian IYD inhibition assay was based on demonstration of sufficient IYD enzyme activity in several tissues collected from larval Xenopus laevis. With this new assay, 154 chemicals were tested in concentration-response to provide a basis for comparison of relative chemical potency to results obtained from the human IYD assay. Most chemicals exhibited similar inhibition in both assays, with less than 25% variation in median inhibition for 120 of 154 chemicals and 85% concordance in categorization of “active” (potential IYD inhibitor) versus “inactive”. For chemicals that produced 50% or greater inhibition in both assays, rank-order potency was similar, with the majority of the IC50s varying by less than 2-fold (and all within an order of magnitude). Most differences resulted from greater maximum inhibition or higher chemical potency observed with human IYD. This strong cross-species agreement suggests that results from the human-based assay would be conservatively predictive of chemical effects on amphibian IYD.

Record Details:

Record Type:DOCUMENT( JOURNAL/ PEER REVIEWED JOURNAL)
Product Published Date:06/26/2022
Record Last Revised:01/22/2024
OMB Category:Other
Record ID: 356102