| Literature DB >> 35716044 |
Rob Knight1,2,3, Emma Board-Davies1,2, Helen Brown1,2, Aled Clayton2,4, Terence Davis3, Ben Karatas2,5, James Burston2,5,6, Zsuzsanna Tabi3, Juan M Falcon-Perez7,8,9, Stephen Paisey2,3, Phil Stephens1,2.
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.Entities:
Keywords: immortalization; oral mucosa; regenerative medicine; scarless wound healing; scarring; small extracellular; stem cells; vesicles
Mesh:
Year: 2022 PMID: 35716044 PMCID: PMC9397654 DOI: 10.1093/stcltm/szac037
Source DB: PubMed Journal: Stem Cells Transl Med ISSN: 2157-6564 Impact factor: 7.655