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Published on: January 14, 2021
A two-component pre-seeded dermal-epidermal scaffold
I P Monteiro1, D Gabriel2, B P Timko2
1Laboratory for Biomaterials and Drug Delivery, Department of Anesthesiology, Division of Critical Care Medicine, Children's Hospital Boston, Harvard Medical School, 300 Longwood Avenue, Boston, MA 02115, USA; Department of Chemical Engineering, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, MA 02139, USA; 3B's Research Group - Biomaterials, Biodegradables and Biomimetics, University of Minho, Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine, AvePark, 4806-909 Taipas, Guimarães, Portugal; ICVS/3B's - PT Government Associate Laboratory University of Minho, Braga/Guimarães, Portugal.
Researchers created a new bilayered skin scaffold to treat full-thickness skin defects. This innovative scaffold supports fibroblast and keratinocyte growth, mimicking natural skin for potential therapeutic applications.
Area of Science:
- Biomaterials Science
- Tissue Engineering
- Regenerative Medicine
Background:
- Full-thickness skin defects pose significant clinical challenges requiring advanced regenerative solutions.
- Current treatments often face limitations in promoting complete skin regeneration and functional recovery.
Purpose of the Study:
- To develop and characterize a novel bilayered dermal-epidermal scaffold for treating full-thickness skin defects.
- To evaluate the scaffold's ability to support dermal fibroblast and epidermal keratinocyte proliferation and organization.
Main Methods:
- Fabrication of a bilayered scaffold with a dermal component (fibrin, cross-linked hyaluronic acid, cell adhesion peptide) and an epidermal component (cross-linked hyaluronic acid, poly-l-lysine).
- In situ gelation of the dermal component to conform to lesion shape, delivering human dermal fibroblasts.
- Culturing human keratinocytes on the epidermal membrane.
- Assessing cell attachment, proliferation, matrix formation, and scaffold integrity.
Main Results:
- The dermal component successfully delivered fibroblasts, which formed a three-dimensional matrix facilitated by tailored mechanical properties and cell-binding ligands.
- The epidermal component supported keratinocyte attachment and monolayer formation.
- Stable composite scaffold formation was achieved through amine-aldehyde bonding at the interface.
- Scaffold components provided cell-specific cues promoting proliferation and mimicking the native skin environment.
Conclusions:
- The developed bilayered scaffold effectively supports both dermal and epidermal cell growth and organization.
- This scaffold shows promise as a biomimetic construct for the treatment of full-thickness skin defects.
- Further investigation is warranted to assess in vivo efficacy and clinical translation.
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