间质细胞
生物
角膜
基质
转录组
细胞生物学
细胞
诱导多能干细胞
电池类型
干细胞
基因表达谱
角膜病
角膜疾病
干细胞标记物
角膜上皮
细胞分化
细胞培养
单细胞分析
细胞迁移
细胞命运测定
角膜移植
作者
Pere Català,Nathalie Gröen,Jasmin A. Dehnen,Eduardo Soares,Arianne J.H. van Velthoven,Rudy M.M.A. Nuijts,Mor M. Dickman,Vanessa L.S. LaPointe
标识
DOI:10.1038/s41598-021-01015-w
摘要
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.
科研通智能强力驱动
Strongly Powered by AbleSci AI