| dc.description.abstract | Exosomes are nano-scale and closed membrane vesicles which are promising for therapeutic applications due to exosome-enclosed therapeutic molecules such as DNA, small RNAs, proteins, and lipids. Recently, it has been demonstrated that mesenchymal stem cell (MSC)-derived exosomes have the capacity to regulate many biological events associated with the wound healing process, such as cell proliferation, cell migration, and blood vessel formation. This study investigated the regenerative potentials for cutaneous tissue, in regard to growth factors associated with wound healing and skin cell proliferation and migration, by exosomes released from primary MSCs originated from bone marrow (BM), adipose tissue (AD), and umbilical cord (UC) under serum- and xeno-free conditions. We found crucial wound healing-mediated growth factors, such as vascular endothelial growth factor A (VEGF-A), fibroblast growth factor 2 (FGF-2), hepatocyte growth factor (HGF), and platelet-derived growth factor BB (PDGF-BB) in exosomes derived from all three MSC sources. However, expression levels of these growth factors in exosomes were influenced by MSC origins, especially transforming growth factor beta (TGF-β), which was only detected in UCMSC-derived exosomes. All exosomes released by the three MSC sources induced keratinocyte and fibroblast proliferation and migration; and the induction of cell migration was dependent on the dosage of exosomes used (20 μg), with a faster migration rate observed at higher doses. Additionally, the influences of exosomes on cell proliferation and migration were associated with exosome origins and also the target cells of exosomes, with the greatest induction of primary dermal fibroblasts belonging to BMMSC-derived exosomes and keratinocytes belonging to UCMSC-derived exosomes. Data from this study indicated that BMMSCs and UCMSCs under clinical conditions secreted exosomes that are promising to develop into therapeutic products for wound healing treatment. | en_US |
