Clinical Grade Human Pluripotent Stem Cell-Derived Engineered Skin Substitutes Promote Keratinocytes Wound Closure In Vitro.
Sophie DominguesAnnabelle DarleYolande MassonManoubia SaidaniEmilie LagoutteAna BejanariuJulien CoutierRaif Eren AyataMarielle BouschbacherMarc PeschanskiGilles LemaîtreChristine BaldeschiPublished in: Cells (2022)
Chronic wounds, such as leg ulcers associated with sickle cell disease, occur as a consequence of a prolonged inflammatory phase during the healing process. They are extremely hard to heal and persist as a significant health care problem due to the absence of effective treatment and the uprising number of patients. Indeed, there is a critical need to develop novel cell- and tissue-based therapies to treat these chronic wounds. Development in skin engineering leads to a small catalogue of available substitutes manufactured in Good Manufacturing Practices compliant (GMPc) conditions. Those substitutes are produced using primary cells that could limit their use due to restricted sourcing. Here, we propose GMPc protocols to produce functional populations of keratinocytes and fibroblasts derived from pluripotent stem cells to reconstruct the associated dermo-epidermal substitute with plasma-based fibrin matrix. In addition, this manufactured composite skin is biologically active and enhances in vitro wounding of keratinocytes. The proposed composite skin opens new perspectives for skin replacement using allogeneic substitute.
Keyphrases
- wound healing
- healthcare
- soft tissue
- pluripotent stem cells
- end stage renal disease
- primary care
- chronic kidney disease
- endothelial cells
- oxidative stress
- stem cell transplantation
- stem cells
- prognostic factors
- cell death
- cell therapy
- cell cycle arrest
- social media
- drug induced
- smoking cessation
- hematopoietic stem cell