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Published on: December 19, 2018
Assessing Indoor Dust Interference with Human Nuclear Hormone Receptors in Cell-Based Luciferase Reporter Assays
Anna S Young1,2, Thomas Zoeller3, Russ Hauser1
1Department of Environmental Health, Harvard T.H. Chan School of Public Health, Boston, Massachusetts, USA.
Background:
Per- and polyfluoroalkyl substances (PFAS), organophosphate esters (OPEs), and polybrominated diphenyl ethers (PBDEs) are hormone-disrupting chemicals that migrate from building materials into air and dust.
Objectives:
We aimed to quantify the hormonal activities of 46 dust samples and identify chemicals driving the observed activities.
Methods:
We evaluated associations between hormonal activities of extracted dust in five cell-based luciferase reporter assays and dust concentrations of 42 measured PFAS, OPEs, and PBDEs, transformed as either raw or potency-weighted concentrations based on Tox21 high-throughput screening data.
Results:
All dust samples were hormonally active, showing antagonistic activity toward peroxisome proliferator-activated receptor () (100%; 46 of 46 samples), thyroid hormone receptor () (89%; 41 samples), and androgen receptor (AR) (87%; 40 samples); agonist activity on estrogen receptor () (96%; 44 samples); and binding competition with thyroxine () on serum transporter transthyretin (TTR) (98%; 45 samples). Effects were observed with as little as of extracted dust. In regression models for each chemical class, interquartile range increases in potency-weighted or unknown-potency chemical concentrations were associated with higher hormonal activities of dust extracts (potency-weighted: , , ; , , ; , , ; , , ; unknown-potency: , , ; , , ), adjusted for chemicals with active, inactive, and unknown Tox21 designations.
Discussion:
All indoor dust samples exhibited hormonal activities, which were associated with PFAS, PBDE, and OPE levels. Reporter gene cell-based assays are relatively inexpensive, health-relevant evaluations of toxic loads of chemical mixtures that building occupants are exposed to. https://doi.org/10.1289/EHP8054.

