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Updated: Dec 9, 2025

Author Spotlight: In Vivo Assessment of Thyroid Hormone Disruption Using the THAI Mouse Model
Published on: October 6, 2023
[Thyroid disruptor p, p'-DDE inhibited the expression of LHX4 and DIS3L protein in Nthy-ori-3-1 cells]
Abstract:
Objective: To observe the changes of LHX4 and DIS3L mRNA and protein expression in Nthy-ori-3-1 cells after the treatment of thyroid disruptor p, p'-DDE. Methods: Nthy-ori-3-1 cells in logarithmic growth phase were treated with 0, 0.5, 1.0, 2.0 and 5.0 μg/ml p, p'-DDE solution. The growth state and morphology of the cells were observed by microscope. The mRNA levels of LHX4 and DIS3L were detected by real-time fluorescent quantitative PCR, and the protein expression levels of LHX4 and DIS3L were detected by Western blot. Results: when the concentrations of p, p'-DDE were 0, 0.5, 1.0 and 2.0 μg/ml, Nthy-ori-3-1 cells grew normally. There were 33 differential genes in 2.0 μg/ml group, among which 13 genes were down regulated and 20 genes were up-regulated. Compared with the control group, the protein expression levels of LHX4 and DIS3L in 1.0 and 2.0 μg/ml groups were significantly decreased (P<0.05) , and the relative expression levels of LHX4 and DIS3L protein mRNA in 1.0 μg/ml group were significantly decreased (P<0.05) . Conclusion: p, p'-DDE can affect the protein expression of LHX4 and dis3l in nthy-ori-3-1 cells.
Insights
The thyroid disruptor p,p'-DDE significantly decreases LHX4 and DIS3L protein and mRNA expression in Nthy-ori-3-1 cells. This indicates p,p'-DDE impacts cellular processes regulated by these key genes.
Area of Science:
- Endocrinology
- Molecular Biology
- Environmental Toxicology
Background:
- Thyroid disruptors pose risks to human health.
- Understanding the molecular mechanisms of thyroid disruptors is crucial.
Purpose of the Study:
- To investigate the effects of p,p omino'-DDE on LHX4 and DIS3L gene and protein expression.
- To assess the impact of p,p omino'-DDE on Nthy-ori-3-1 cell lines.
Main Methods:
- Nthy-ori-3-1 cells were treated with varying concentrations of p,p omino'-DDE.
- Real-time fluorescent quantitative PCR was used to measure mRNA levels.
- Western blot analysis was performed to quantify protein expression.
Main Results:
- p,p omino'-DDE exposure led to significant decreases in LHX4 and DIS3L protein expression at concentrations of 1.0 and 2.0 μg/ml.
- mRNA levels of LHX4 and DIS3L were also significantly reduced in the 1.0 μg/ml group.
- Gene expression profiling revealed 33 differentially expressed genes at 2.0 μg/ml p,p omino'-DDE.
Conclusions:
- p,p omino'-DDE exposure negatively affects LHX4 and DIS3L expression in Nthy-ori-3-1 cells.
- The study highlights the potential of p,p omino'-DDE to disrupt cellular functions through modulation of these genes.
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