Related Experiment Video
Updated: May 1, 2026

08:20
In Vitro Model of Human Cutaneous Hypertrophic Scarring using Macromolecular Crowding
Published on: May 1, 2020
6.4K
Human hypertrophic and keloid scar models: principles, limitations and future challenges from a tissue engineering
Lenie J van den Broek1, Grace C Limandjaja, Frank B Niessen
1Department of Dermatology, VU University Medical Center, Amsterdam, The Netherlands; Research Institute MOVE, Amsterdam, The Netherlands.
Experimental Dermatology
|April 23, 2014
Summary
Current scar models fail to explain why abnormal scars form. Future research must address genetic and immune factors for scar-free healing strategies and new drug targets.
Area of Science:
- Wound healing research
- Regenerative medicine
- Dermatology
Background:
- Most cutaneous wounds heal with scarring, but abnormal scars like hypertrophic scars and keloids can develop.
- Preventing adverse scar formation and understanding individual predispositions remain significant challenges in clinical practice and scientific research.
- Existing models for studying scar formation have limitations in addressing the specific mechanisms differentiating normotrophic, hypertrophic, and keloid scars.
Purpose of the Study:
- To review current in vitro and animal models for scar formation research.
- To highlight the limitations of existing models in explaining the development of abnormal scars.
- To identify future challenges and research directions for achieving scar-free wound healing.
Main Methods:
- Review of existing literature on scar formation models, including cell cultures, tissue-engineered models, and humanized mouse models.
- Analysis of the capabilities and limitations of current models in addressing key questions about scar development.
- Identification of knowledge gaps concerning the transition from normotrophic to abnormal scarring.
Main Results:
- Current high- and medium-throughput models do not adequately address why adverse scars form instead of normotrophic ones.
- Existing models struggle to differentiate the causes of hypertrophic scars versus keloids.
- The role of individual genetic predisposition and the immune system in scar formation is not fully elucidated by current models.
Conclusions:
- Significant limitations exist in current in vitro and animal models for studying scar formation.
- Understanding the genetic and immune system's involvement is crucial for developing effective scar prevention strategies.
- Future research must focus on developing advanced models that can address these complexities to achieve scar-free healing.

