Eye Center, Medical Center, Faculty of Medicine, University of Freiburg, Killianstrasse 5, 79106, Freiburg, Germany.
Department of Ophthalmology, University Hospital Erlangen, Friedrich-Alexander-University of Erlangen-Nürnberg, Schwabachanlage 6, 91054, Erlangen, Germany.
Sci Rep. 2020 Oct 16;10(1):17588. doi: 10.1038/s41598-020-74869-1.
Limbal melanocytes (LM) are located in the basal epithelial layer of the corneoscleral limbus and interact with adjacent limbal epithelial progenitor cells. The exploration of their biological role in the maintenance of the limbal stem cell niche has been limited by the difficulty of LM isolation and cultivation. Here, we report on a facile protocol for the efficient isolation and enrichment of pure populations of human LMs by fluorescence-activated cell sorting (FACS) using antibodies raised against the cell surface marker CD117 (c-Kit). The enriched LMs retain self-renewal capacity and sustained melanin production, and are suitable to study the potential of LMs in stem cell-based corneal tissue engineering.
角膜缘黑素细胞(LM)位于角巩膜缘的基底上皮层,与相邻的角膜缘上皮祖细胞相互作用。由于 LM 分离和培养困难,限制了对其在维持角膜缘干细胞龛位中的生物学作用的探索。在这里,我们报告了一种使用针对细胞表面标志物 CD117(c-Kit)的抗体通过荧光激活细胞分选(FACS)高效分离和富集纯人群人 LM 的简便方案。富集的 LM 保持自我更新能力和持续的黑色素产生,并且适合于研究 LM 在基于干细胞的角膜组织工程中的潜力。