Journal
ACTA OPHTHALMOLOGICA
Volume 95, Issue 8, Pages e693-e705Publisher
WILEY
DOI: 10.1111/aos.13371
Keywords
cornea regeneration; serum eye drops; s-PRGF; wound healing
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Funding
- University of the Basque Country/Instituto Clinico Quirurgico de Oftalmologia [US11/24]
- University of the Basque Country [UFI11/44]
- Saiotek Program of the Basque Government [S-PE12UN128]
- Mutua Madrilena Foundation [FMM11/02]
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PurposeTo evaluate the regenerating potential and the mechanisms through which the autologous serum derived from plasma rich in growth factors (s-PRGF) favours corneal wound healing invitro and invivo. MethodsWe compared the effect of various concentrations of s-PRGF versus fetal bovine serum (FBS) and control treatment in rabbit primary corneal epithelial and stromal cells and wounded rabbit corneas. Cell proliferation was measured using an enzymatic colorimetric assay. In vitro and invivo wound-healing progression was assessed by image-analysis software. Migration and invasion were evaluated using transfilter assays. Histological structure was analysed in stained sections. Protein expression was evaluated by immunohistochemistry. Resultss-PRGF promoted the robust proliferation of epithelial cultures at any concentration, similar to FBS. Likewise, s-PRGF and FBS produced similar re-epithelialization rates in invitro wound-healing assays. In vivo, s-PRGF treatment accelerated corneal wound healing in comparison with control treatment. This difference was significant only for 100% s-PRGF treatment in our healthy rabbit model. Histological analysis confirmed normal epithelialization in all cases. Immunohistochemistry showed a higher expression of cytokeratins 3/76 and 15, zonula occludens-1 and alpha-smooth muscle actin proteins as a function of s-PRGF concentration. Notably, keratocyte density in the anterior third of the stroma increased with increase in s-PRGF concentration, suggesting an invivo chemotactic effect of s-PRGF on keratocytes that was further confirmed invitro. Conclusions-PRGF promotes proliferation and migration and influences limbal stemness, adhesion and fibrosis during corneal healing.
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