In vivo, epithelial cells are connected both anatomically and functionally with stromal keratocytes. In vitro co-culturing aims to recapture this cellular anatomy and functionality by bringing together two or more cell types within the same culture environment. The aim of this study was to investigate epithelial-stromal cell signalling for the control of corneal stromal cell plasticity in 3D culture models.Methods
Corneal stromal cells were activated to their injury phenotype (fibroblasts) before being encapsulated in 3D collagen hydrogels. 3 different epithelial-stromal co-culture methods were then examined; epithelial explant; transwell; the use of conditioned media. Using non-destructive monitoring tools we revealed how epithelial co-culturing affects stromal cell differentiation in terms of construct contraction and elastic modulus measurements in a 3D collagen hydrogel environment for prolonged culture periods. Cell viability, phenotype, morphology and protein expression was investigated to corroborate our mechanical findings.Results
It was shown that activated stromal cells retain their plasticity in vitro. Activated corneal stromal cells that were fibroblastic in phenotype were successfully reverted to a non-activated keratocyte cell lineage in terms of behaviour and biological properties; and then back again via TGF-β1 media supplementation. It was then revealed that epithelial-stromal interactions can be blocked via the use of wortmannin inhibition.Conclusion
A greater understanding of stromal-epithelial interactions and what mediates them offers great pharmacological potential in the regulation of corneal wound healing, with the potential to treat corneal diseases and injury whereby such interactions are vital.