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Updated: May 19, 2026

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Assessment of Acute Wound Healing using the Dorsal Subcutaneous Polyvinyl Alcohol Sponge Implantation and Excisional Tail Skin Wound Models.
Published on: March 25, 2020
Assessment of Acute Wound Healing Using Excisional Mouse Tail Skin Wound Models
Iqra Fatima1, Andrey A Sharov2
1Department of Dermatology, Boston University Chobanian and Avedisian School of Medicine, Boston, MA, USA.
Methods in Molecular Biology (Clifton, N.J.)
|May 18, 2026
Summary
A new mouse tail wound model offers a better way to study skin healing. This reproducible method aids research into chronic wounds like diabetic foot ulcers and venous leg ulcers.
Area of Science:
- Regenerative Medicine
- Dermatology
- Translational Research
Background:
- Wound healing is a complex biological process crucial for restoring skin barrier function after injury.
- Chronic wounds, including diabetic foot and venous leg ulcers, affect millions, incurring significant healthcare costs and morbidity.
- Current in vivo models, like the back-punch excisional model, have limitations in mimicking human wound healing due to predominant contraction and reduced granulation tissue formation.
Purpose of the Study:
- To present a detailed and reproducible protocol for creating excisional wounds on mouse tails.
- To establish a model that overcomes the limitations of traditional wound healing models, promoting robust granulation and epithelialization.
- To optimize the mouse tail excisional model for downstream analyses, including histology, cryosectioning, and single-cell multi-omic studies.
Main Methods:
- Development and refinement of a standardized protocol for generating excisional wounds on the mouse tail.
- Characterization of wound healing dynamics, including granulation tissue formation and reepithelialization, in the tail model.
- Optimization of tissue processing for histological and cryosectioning analyses.
- Adaptation of the model for efficient single-cell isolation for multi-omic investigations.
Main Results:
- The mouse tail excisional model demonstrates robust granulation tissue formation and epithelial coverage, attributed to the "splinting" effect of the tail structure.
- This model provides a more physiologically relevant representation of wound healing compared to the back-punch model, which is dominated by contraction.
- The protocol is optimized for high-quality histological and cryosectioned samples, facilitating detailed cellular and molecular analysis.
- The model supports effective downstream cell isolation for advanced single-cell multi-omic analyses.
Conclusions:
- The mouse tail excisional wound model offers a superior alternative for studying wound healing mechanisms, particularly for chronic wound research.
- This reproducible protocol facilitates detailed investigation into the cellular and molecular regulators of skin repair.
- The model's suitability for histology, cryosectioning, and single-cell multi-omics enables comprehensive multi-level analyses of wound healing processes.

