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Noise Stress Induces an Epidermal Growth Factor Receptor/Xeroderma Pigmentosum-A Response in the Auditory Nerve
O'neil W Guthrie1,2,3
1Cell & Molecular Pathology Laboratory, Department of Communication Sciences and Disorders, Northern Arizona University, Flagstaff, Arizona (OWG).
Abstract:
In response to toxic stressors, cancer cells defend themselves by mobilizing one or more epidermal growth factor receptor (EGFR) cascades that employ xeroderma pigmentosum-A (XPA) to repair damaged genes. Recent experiments discovered that neurons within the auditory nerve exhibit basal levels of EGFR+XPA co-expression. This finding implied that auditory neurons in particular or neurons in general have the capacity to mobilize an EGFR+XPA defense. Therefore, the current study tested the hypothesis that noise stress would alter the expression pattern of EGFR/XPA within the auditory nerve. Design-based stereology was used to quantify the proportion of neurons that expressed EGFR, XPA, and EGFR+XPA with and without noise stress. The results revealed an intricate neuronal response that is suggestive of alterations to both co-expression and individual expression of EGFR and XPA. In both the apical and middle cochlear coils, the noise stress depleted EGFR+XPA expression. Furthermore, there was a reduction in the proportion of neurons that expressed XPA-alone in the middle coils. However, the noise stress caused a significant increase in the proportion of neurons that expressed EGFR-alone in the middle coils. The basal cochlear coils failed to mobilize a significant response to the noise stress. These results suggest that EGFR and XPA might be part of the molecular defense repertoire of the auditory nerve.
Insights
Noise stress alters the expression of epidermal growth factor receptor (EGFR) and xeroderma pigmentosum-A (XPA) in auditory neurons. This suggests EGFR and XPA are part of the auditory nerve
Area of Science:
- Neuroscience
- Molecular Biology
- Genetics
Background:
- Cancer cells utilize epidermal growth factor receptor (EGFR) and xeroderma pigmentosum-A (XPA) for gene repair against toxic stressors.
- Auditory neurons were found to possess basal levels of EGFR and XPA co-expression.
- This suggests a potential defensive role for EGFR/XPA in neurons.
Purpose of the Study:
- To investigate the impact of noise stress on the expression patterns of EGFR and XPA within the auditory nerve.
- To test the hypothesis that noise stress alters EGFR/XPA co-expression and individual expression in auditory neurons.
Main Methods:
- Utilized design-based stereology for quantitative analysis.
- Compared EGFR, XPA, and EGFR+XPA expression in auditory neurons with and without noise stress exposure.
- Examined expression across different cochlear coils (apical, middle, basal).
Main Results:
- Noise stress significantly altered EGFR and XPA expression in the apical and middle cochlear coils.
- EGFR+XPA co-expression decreased in apical and middle coils following noise stress.
- Middle coils showed reduced XPA-alone expression but increased EGFR-alone expression.
- Basal cochlear coils did not exhibit a significant response to noise stress.
Conclusions:
- The study suggests that EGFR and XPA are involved in the molecular defense mechanisms of the auditory nerve.
- Noise stress induces complex changes in EGFR and XPA expression, indicating a neuronal response.
- The findings highlight a potential role for these proteins in protecting auditory neurons from environmental stressors.
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