3D Living Dressing Improves Healing and Modulates Immune Response in a Thermal Injury Model.
Paul R TurnerMichelle McConnellSarah L YoungJaydee Dones CabralPublished in: Tissue engineering. Part C, Methods (2022)
Thermal injury trauma can induce a state of immunosuppression, causing wounds to become chronic in nature. Stem cell-based therapies represent a promising new approach to treat such wounds due to their capacity to self-renew and their multi-lineage potential. Mesenchymal stem cells (MSCs) are known to secrete endogenous factors that stimulate wound healing by promoting angiogenesis, extracellular matrix remodeling, skin regeneration, and by dampening down inflammation. MSC delivery in a biomaterial construct can augment their wound-healing capacity by concentrating cells at the burn site and upregulating trophic factor secretion. The work presented is the first to evaluate repair in an in vitro raft thermal injury model using a regenerative, dual cell delivery three-dimensional (3D) core/shell (c/s) "living dressing" construct. This previously characterized 3D c/s bioprinted construct, which delivers both MSCs and endothelial cells, was used to treat an in vitro 3D raft skin thermal injury wound model. The mesenchymal stromal cell line (T0523) was encapsulated within a gelatin-based shell bioink, and human umbilical vein endothelial cells within a chitosan-based core bioink to biofabricate a living dressing for enhanced thermal injury repair and regeneration. We hypothesized that the cell-laden c/s tissue engineered construct (TEC) would strengthen the wound's proangiogenic, anti-inflammatory, and skin regeneration potential. An in vitro thermal injury in a 3D raft skin model showed a slight delay in wound closure in the presence of the c/s TEC but was augmented by corresponding increases in the release of wound-healing factors, epidermal growth factor, matrix metalloproteinases-9, transforming growth factor-α, platelet-derived growth factor; a decrease in pro-inflammatory factor interleukin-6, and evidence of neovascularization.
Keyphrases
- wound healing
- growth factor
- mesenchymal stem cells
- stem cells
- endothelial cells
- immune response
- cell therapy
- transforming growth factor
- extracellular matrix
- single cell
- bone marrow
- induced apoptosis
- umbilical cord
- oxidative stress
- anti inflammatory
- epithelial mesenchymal transition
- vascular endothelial growth factor
- signaling pathway
- risk assessment
- climate change
- cell death
- endoplasmic reticulum stress
- high glucose
- virtual reality
- soft tissue