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Establishing a Mouse Model of Surgical Vocal Fold Injury
Akari Kimura1, Mohammed Imran Khan1, Meena Easwaran1
1Department of Otolaryngology - Head & Neck surgery, School of Medicine, Stanford University, Stanford, California, USA.
The Laryngoscope
|August 24, 2024
Summary
Researchers developed a new mouse model for vocal fold (VF) surgical injury. This accessible method aids in studying VF wound healing and scar formation in the epithelium and lamina propria.
Area of Science:
- Otolaryngology
- Regenerative Medicine
- Surgical Pathology
Background:
- Vocal fold (VF) surgical injury and subsequent scar formation are significant clinical challenges.
- Existing animal models for VF injury may lack accessibility or utilize specialized materials.
- Understanding VF wound healing is crucial for improving surgical outcomes and voice restoration.
Purpose of the Study:
- To establish a practical and accessible alternative animal model for inducing unilateral vocal fold (VF) surgical injury in mice.
- To investigate the epithelial (EP) and lamina propria (LP) wound healing responses following this induced VF injury.
Main Methods:
- Mice underwent unilateral VF injury induced by a wire brush under laryngoscopic visualization.
- Injured VFs were harvested at multiple time points (1-28 days) post-injury.
- Histological and immunofluorescent analyses assessed EP thickness, LP area, cell proliferation (Ki67), basal cell markers (p63), and collagen III deposition.
Main Results:
- The injury reached the superficial thyroarytenoid muscle by Day 1.
- Increased EP thickness and LP area were observed from Day 3 onwards.
- Elevated cell proliferation (Ki67+, p63+) occurred on Day 3, with increased collagen III content noted on Days 5 and 28.
Conclusions:
- A reproducible and accessible mouse model for unilateral vocal fold surgical injury was successfully established.
- This model provides a valuable platform for future research into VF surgical injury mechanisms and therapeutic interventions.
- The findings offer insights into the dynamic wound healing processes within the VF epithelium and lamina propria.

