Objectives: Skin aging is subject of many studies in esthetic surgery including several morphological changes like decrease of epidermis thickness and of cell proliferative potential. ASC, mesenchymal stem cells derived from adipose tissue, have been used in regenerative and reparative surgery as well as anti-aging solution. The aim of this study was to highlight the influence of ASCs on skin aging and healing in an in vitro skin model. Methods: Using an skin equivalent (SE) model prepared without or with ASCs in different proportion (25% or 50% of ASCs), beneficial influence of ASCs on epidermal regeneration via markers of proliferative and differentiative potential and on quality of the dermis via markers of dermal protein synthesis was analyzed. In addition, an extendedtime cultured model mimicking skin ageing was used to demonstrate ASCs influence on skin aging via markers of the quality of the epidermis and dermis as well as via a marker of senescence. Results: After 42 days of culture, SEs prepared with 25% of ASCs were thicker, presented a better proliferative potential showed by a higher number of Ki67 positive cells, and a better differentiation in epidermis. A better fibroblast synthesis in dermis was also showed. Skin ageing was studied by prolonging culture time : SEs prepared with 25% of ASCs showed remained Ki67 positive cells and a low level of senescent marker, p16, labeling, whereas SEs with fibroblasts alone were very thin, free of proliferative cells and with a high p16 expression. Conclusions: To conclude, adding ASCs in low proportion (25%) improved quality of the epidermis and dermis preventing senescence of the SE model. This confirms clinical results and supports their anti-aging effect and their potential in wound healing. In addition, this model provides a tool to elucidate the mode of action of ASCs on healing and skin aging.
CITATION STYLE
Odile Damour, M. D. (2014). Adipose-derived Stem Cells Promote Skin Homeostasis and Prevent its Senescence in an In vitro Skin Model. Journal of Stem Cell Research & Therapy, 04(04). https://doi.org/10.4172/2157-7633.1000194
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