Related Experiment Video
Updated: Jun 13, 2025

04:14
Author Spotlight: In Vivo Assessment of Thyroid Hormone Disruption Using the THAI Mouse Model
Published on: October 6, 2023
784
In Vitro Screening for ToxCast Chemicals Binding to Thyroxine-Binding Globulin
Stephanie A Eytcheson1,2, Alexander D Zosel2,3, Jennifer H Olker2
1Oak Ridge Institute for Science and Education Postdoctoral Fellow, Oak Ridge, Tennessee 37830, United States.
Chemical Research in Toxicology
|September 13, 2024
Summary
This study screened over 1,400 chemicals for their ability to disrupt thyroid hormone (TH) transport by binding to thyroxine-binding globulin. Several potent chemicals were identified, aiding in the prediction of in vivo effects.
Area of Science:
- Endocrinology
- Toxicology
- Biochemistry
Background:
- Thyroid hormone (TH) carrier proteins are crucial for TH distribution and homeostasis.
- Disruption of TH carrier proteins is a potential mechanism for thyroid system dysfunction.
- Limited data exists on chemicals that bind to TH carrier proteins and displace TH.
Purpose of the Study:
- To screen a large chemical library for compounds that competitively bind to thyroxine-binding globulin (TBG).
- To identify chemicals that interfere with thyroid hormone transport and homeostasis.
- To develop and validate an in vitro assay for high-throughput screening of endocrine disruptors.
Main Methods:
- A fluorescence-based in vitro screening assay was employed.
- Over 1,400 chemicals from U.S. EPA's ToxCast libraries were screened.
- Chemicals showing competitive binding to TBG were further analyzed in concentration-response studies.
Main Results:
- 714 out of 1,400+ chemicals showed inhibition of bound fluorescent ligand at 100 μM.
- 297 chemicals exhibited ≥50% reduction in fluorescence and underwent further testing.
- Ten chemicals demonstrated EC50 values <1 μM, indicating high potency in disrupting TH binding.
Conclusions:
- The developed in vitro assay effectively identifies chemicals that can disrupt thyroid hormone homeostasis.
- Results support prioritizing chemicals for in vivo testing to predict real-world effects.
- This work expands the toolkit for identifying potential endocrine-disrupting chemicals.

