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Author Spotlight: Advancements in the Fabrication of Synthetic Vocal Fold Models for Phonetic and Robotic Applications
Published on: January 5, 2024
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In vitro model to evaluate effect of acidic pepsin on vocal fold barrier function
Keisuke Kojima1, Tatsuya Katsuno2, Yo Kishimoto3
1Kojima ENT Clinic, Kyoto, Japan.
Biochemical and Biophysical Research Communications
|July 21, 2024
Summary
Laryngopharyngeal reflux (LPR) damages vocal fold barrier functions. An in vitro model shows acidic pepsin injures tight junctions, but vocal fold cells repair within one day.
Area of Science:
- Otolaryngology
- Cell Biology
- Biochemistry
Background:
- Laryngopharyngeal reflux (LPR) pathophysiology and vocal fold impact are unclear.
- Vocal fold barrier function involves mucus and tight junctions.
- Acidic damage may compromise these barriers.
Purpose of the Study:
- Develop an in vitro system to study vocal fold barrier injury and repair.
- Evaluate the effects of acidic pepsin on vocal fold epithelium.
Main Methods:
- Established a rat vocal fold epithelial in vitro model.
- Exposed the model to acidic pepsin for injury assessment.
- Monitored tight junction permeability and microprojection integrity.
Main Results:
- The in vitro model survived over a week post-maturation.
- Acidic pepsin injured tight junctions and microprojections.
- Both tight junctions and microprojections healed within 24 hours.
- Acidic pepsin increased permeability more than acid alone.
- Pepsin primarily affected protein-based tight junctions.
Conclusions:
- The developed in vitro system effectively models vocal fold chemical injury and repair.
- Acidic pepsin's proteolytic action significantly impacts vocal fold barrier function.
- Findings advance understanding of LPR pathogenesis and vocal fold injury recovery.
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