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Abstract
Secretomes from various cell sources exert strong regenerative activities on numerous organs, including the skin. Although secretomes consist of many diverse components, a growing body of evidence suggests that small extracellular vesicles (EVs) account for their regenerative capacity. We previously demonstrated that the secretome of γ-irradiated peripheral blood mononuclear cells (PBMCs) exhibits wound healing capacity. Therefore, we sought to dissect the molecular composition of EVs present in the secretome and compared wound healing-related activities of these EVs to other subfractions of the secretome and the fully supplemented secretome (MNCaposec). Compared to EVs derived from non-irradiated PBMCs, γ-irradiation significantly increased the size and number and changed the composition of released EVs. Detailed characterization of the molecular components of EVs, i.e. miRNA, proteins, and lipids, derived from irradiated PBMCs revealed a strong association with regenerative processes. Reporter gene assays and aortic ring sprouting assays revealed diminished activity of the subfractions compared to MNCaposec. In addition, we showed that MNCaposec accelerated wound closure in a diabetic mouse model. Taken together, our results suggest that secretome-based wound healing represents a promising new therapeutic avenue, and strongly recommend using the complete secretome instead of purified subfractions, such as EVs, to exploit its full regenerative capacity.
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1 Division of Thoracic Surgery, Medical University of Vienna, Vienna, Austria
2 Department of Cardiology, Department of Internal Medicine II, Medical University of Vienna, Vienna, Austria
3 Department of Biomedical Imaging and Image-guided Therapy, Medical University of Vienna, Vienna, Austria
4 Research Division of Biology and Pathobiology of the Skin, Department of Dermatology, Medical University of Vienna, Vienna, Austria
5 Molecular Neuro-Oncology Research Unit, Department of Pediatrics and Adolescent Medicine and Institute of Neurology, Medical University of Vienna, Vienna, Austria
6 Synlab, Birsfelden, Switzerland
7 Division of Thoracic Surgery, Medical University of Vienna, Vienna, Austria; Department of Cardiology, Department of Internal Medicine II, Medical University of Vienna, Vienna, Austria
8 Clinical Division of Plastic and Reconstructive Surgery, Department of Surgery, Medical University of Vienna, Vienna, Austria
9 Department of Molecular Medicine, Unit of Cardiology, University of Pavia, Pavia, Italy; Coronary Care Unit, Laboratory of Experimental Cardiology for Cell and Molecular Therapy, Fondazione IRCCS Policlinico San Matteo Foundation, Pavia, Italy; Department of Medicine, University of Cape Town, Cape Town, South Africa
10 Red Cross Blood Transfusion Service of Upper Austria, Linz, Austria
11 Ludwig Boltzmann Institute for Experimental and Clinical Traumatology, Vienna, Austria
12 Division of Thoracic Surgery, Medical University of Vienna, Vienna, Austria; FFG Project 852748 “APOSEC”, Medical University of Vienna, Vienna, Austria; Christian Doppler Laboratory for Cardiac and Thoracic Diagnosis and Regeneration, Vienna, Austria