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Assimilating cell sheets and hybrid scaffolds for dermal tissue engineering
Kee Woei Ng1, Wanrong Tham, Thiam Chye Lim
1Department of Surgery, National University of Singapore, 9 Engineering Drive 1, Singapore 117576.
Journal of Biomedical Materials Research. Part A
|August 18, 2005
Summary
Tissue engineering dermal constructs using cell sheets is promising. A novel technique using collagen-hyaluronic acid foams minimizes cell sheet contraction, enabling viable bilayered skin regeneration.
Area of Science:
- Regenerative Medicine
- Tissue Engineering
- Biomaterials Science
Background:
- Cell sheets offer a method for creating neo-tissue with mature extracellular matrix.
- Significant cell sheet contraction poses a challenge in tissue engineering applications.
Purpose of the Study:
- To develop a technique to overcome cell sheet contraction in dermal construct engineering.
- To evaluate the efficacy of collagen-hyaluronic acid foams versus poly(lactic-co-glycolic acid)-collagen meshes for dermal tissue engineering.
Main Methods:
- Human dermal fibroblasts were cultured on poly(lactic-co-glycolic acid)-collagen meshes and collagen-hyaluronic acid foams.
- Cell sheets were folded over scaffolds to create dermal constructs, followed by keratinocyte culture for bilayered skin regeneration assessment.
- Cell proliferation, metabolic activity, viability, F-actin expression, collagen deposition, and growth factor production were analyzed.
Main Results:
- Dermal constructs using collagen-hyaluronic acid foams exhibited minimal contraction, unlike those with poly(lactic-co-glycolic acid)-collagen meshes which curled.
- High cell viability and F-actin expression were observed, along with significant collagen deposition.
- Key growth factors (TGF-α, TGF-β1, KGF, VEGF) were produced, indicating a supportive microenvironment.
Conclusions:
- Integrating cell sheets with mechanically stable scaffolds, specifically collagen-hyaluronic acid foams, yields viable, non-contracting dermal-like constructs.
- This approach eliminates the need for repeated enzymatic cell expansion and overcomes poor scaffold cell seeding efficiency.