Mesenchymal Stem Cell Spheroids Embedded in an Injectable Thermosensitive Hydrogel: An In Situ Drug Formation Platform for Accelerated Wound Healing.
Mohammad Ali NilforoushzadehMohsen Khodadadi YazdiShaghayegh Baradaran GhavamiSamila FarokhimaneshLeila Mohammadi AmirabadPayam ZarrintajMohammad Reza SaebMichael Richard HamblinMehrak ZareMasoud MozafariPublished in: ACS biomaterials science & engineering (2020)
The ability of mesenchymal stem cells (MSCs) to enhance cutaneous wound healing has been well established. Extensive expansion of cells to reach sufficient cell numbers for regenerating tissues has always limited cell-based therapies. An ingenious solution to address this challenge is to develop a strategy to increase the immunomodulatory effects of MSCs without expanding them. In this study, we employed a simple characteristic of cells. It was observed that an optimized three-dimensional (3D) MSC culture in spheroid forms significantly improved their paracrine effects. An electrospray (ES) encapsulation apparatus was used to encapsulate individual or 3D spheroid MSCs into microscale alginate beads (microbeads). Furthermore, alginate microbeads were embedded in an injectable thermosensitive hydrogel matrix, which gels at skin temperature. The hydrogel fills and seals the wounds cavities, maintains high humidity at the wound area, absorbs exudate, and fixes microbeads, protecting them from direct contact with the harsh wound environment. In vitro investigations revealed that secretion of interleukin 10 (IL-0) and transforming growth factor β1 (TGF-β1) gene was gradually enhanced, providing a delivery platform for prolonged release of bioactive molecules. In vivo study on full-thickness wounds showed granulation and re-epithelialization, only after 7 days. Moreover, increased expression of α-smooth muscle actin (α-SMA) in the first 14 days after treatment ensured wound contraction. Besides, a gradual decrease in α-SMA secretion resulted in reduced scar formation. Well-organized collagen fibrils and high expression of the angiogenesis biomarker CD31 confirmed the promoting effect of the hydrogel on the wound-healing process. The proposed wound-dressing system would potentially be used in scalable and effective cell-based wound therapies.
Keyphrases
- wound healing
- mesenchymal stem cells
- transforming growth factor
- umbilical cord
- cell therapy
- smooth muscle
- single cell
- induced apoptosis
- poor prognosis
- epithelial mesenchymal transition
- cell cycle arrest
- gene expression
- high throughput
- oxidative stress
- drug delivery
- genome wide
- bone marrow
- emergency department
- long non coding rna
- hyaluronic acid
- stem cells
- electronic health record
- vascular endothelial growth factor
- dna methylation
- drug induced
- cell death
- endoplasmic reticulum stress