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Human limbal epithelial cells (HLE) and corneal stromal stem cells (CSSC) reside in close proximity  in vivo  in the corneal limbal stem cell niche. However, HLE are typically cultured  in vitro  without supporting niche cells. Here, we re-create the cell-cell juxtaposition of the native environment  in vitro , to provide a tool for investigation of epithelial-stromal cell interactions and to optimize HLE culture conditions for potential therapeutic application. RAFT (Real Architecture For 3D Tissue) tissue equivalents (TEs) were used as a 3-dimensional substrate for co-culturing HLE and CSSC. Our results demonstrate that a monolayer of HLE that maintained expression of p63α, ABCB5, CK8 and CK15 (HLE markers), formed on the surface of RAFT TEs within 13 days of culture. CSSC remained in close proximity to HLE and maintained expression of mesenchymal stem cell markers. This simple technique has a short preparation time of only 15 days with the onset of HLE layering and differentiation observed. Furthermore, co-cultivation of HLE with another niche cell type (CSSC) directly on RAFT TEs, eliminates the requirement for animal-derived feeder cells. RAFT TEs may be useful for future therapeutic delivery of multiple cell types to restore the limbal niche following ocular surface injury or disease.

Human corneal stromal stem cells support limbal epithelial cells cultured on RAFT tissue equivalents