Oral Progenitor Cell Line-Derived Small Extracellular Vesicles as a Treatment for Preferential Wound Healing Outcome

Author:

Knight Rob123,Board-Davies Emma12,Brown Helen12,Clayton Aled24,Davis Terence3,Karatas Ben25,Burston James256,Tabi Zsuzsanna3,Falcon-Perez Juan M789,Paisey Stephen23,Stephens Phil12ORCID

Affiliation:

1. Regenerative Biology Group, Oral and Biomedical Sciences, School of Dentistry, Cardiff University , Cardiff, Wales , UK

2. Cardiff Institute of Tissue Engineering and Repair, Cardiff University , Cardiff, Wales , UK

3. PETIC, School of Medicine, Cardiff University , Cardiff, Wales , UK

4. Division of Cancer and Genetics, School of Medicine, Cardiff University , Cardiff, Wales , UK

5. Systems Immunity Research Institute, School of Medicine, Cardiff University , Cardiff, Wales , UK

6. Division of Infection and Immunity, School of Medicine, Cardiff University , Cardiff, Wales , UK

7. Exosomes Laboratory, Center for Cooperative Research in Biosciences (CIC bioGUNE), Basque Research and Technology Alliance (BRTA) , Derio, Bizkaia , Spain

8. Centro de Investigación Biomédica en Red de enfermedades hepáticas y digestivas (CIBERehd), Instituto de Salud Carlos III , Madrid , Spain

9. IKERBASQUE, Basque Foundation for Science , Bilbao, Bizkaia , Spain

Abstract

Abstract Scar formation during wound repair can be devastating for affected individuals. Our group previously documented the therapeutic potential of novel progenitor cell populations from the non-scarring buccal mucosa. These Oral Mucosa Lamina Propria-Progenitor Cells (OMLP-PCs) are multipotent, immunosuppressive, and antibacterial. Small extracellular vesicles (sEVs) may play important roles in stem cell–mediated repair in varied settings; hence, we investigated sEVs from this source for wound repair. We created an hTERT immortalized OMLP-PC line (OMLP-PCL) and confirmed retention of morphology, lineage plasticity, surface markers, and functional properties. sEVs isolated from OMLP-PCL were analyzed by nanoparticle tracking analysis, Cryo-EM and flow cytometry. Compared to bone marrow–derived mesenchymal stromal cells (BM-MSC) sEVs, OMLP-PCL sEVs were more potent at driving wound healing functions, including cell proliferation and wound repopulation and downregulated myofibroblast formation. A reduced scarring potential was further demonstrated in a preclinical in vivo model. Manipulation of OMLP-PCL sEVs may provide novel options for non-scarring wound healing in clinical settings.

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,General Medicine

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