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Single cell transcriptomics reveals the heterogeneity of the human cornea to identify novel markers of the limbus and stroma

Authors :
Pere Català
Vanessa L.S. LaPointe
Mor M. Dickman
Nathalie Groen
Rudy M.M.A. Nuijts
Eduardo Soares
Jasmin A. Dehnen
Arianne J. H. van Velthoven
CBITE
RS: MHeNs - R3 - Neuroscience
Oogheelkunde
MUMC+: *AB Refractie Chirurgie Oogheelkunde (9)
MUMC+: MA UECM Oogartsen MUMC (9)
MUMC+: MA UECM Oogartsen ZL (9)
RS: MERLN - Cell Biology - Inspired Tissue Engineering (CBITE)
Source :
Scientific Reports, 11(1):21727. Nature Publishing Group, Scientific Reports, Scientific Reports, Vol 11, Iss 1, Pp 1-13 (2021)
Publication Year :
2021
Publisher :
Springer Science and Business Media LLC, 2021.

Abstract

The cornea is the clear window that lets light into the eye. It is composed of five layers: epithelium, Bowman’s layer, stroma, Descemet’s membrane and endothelium. The maintenance of its structure and transparency are determined by the functions of the different cell types populating each layer. Attempts to regenerate corneal tissue and understand disease conditions requires knowledge of how cell profiles vary across this heterogeneous tissue. We performed a single cell transcriptomic profiling of 19,472 cells isolated from eight healthy donor corneas. Our analysis delineates the heterogeneity of the corneal layers by identifying cell populations and revealing cell states that contribute in preserving corneal homeostasis. We identified expression of CAV1, HOMER3 and CPVL in the corneal epithelial limbal stem cell niche, CKS2, STMN1 and UBE2C were exclusively expressed in highly proliferative transit amplifying cells, CXCL14 was expressed exclusively in the suprabasal/superficial limbus, and NNMT was exclusively expressed by stromal keratocytes. Overall, this research provides a basis to improve current primary cell expansion protocols, for future profiling of corneal disease states, to help guide pluripotent stem cells into different corneal lineages, and to understand how engineered substrates affect corneal cells to improve regenerative therapies.

Details

ISSN :
20452322
Volume :
11
Database :
OpenAIRE
Journal :
Scientific Reports
Accession number :
edsair.doi.dedup.....65fdcf7ac808d816735746fc5f221165
Full Text :
https://doi.org/10.1038/s41598-021-01015-w