From the *TissueTech, Inc, and Ocular Surface Center, Miami, FL; †Medical Center for Translational Research, Osaka University Hospital, Osaka Japan; ‡Department of Ophthalmology, Osaka University Graduate School of Medicine, Osaka, Japan; §Eye Institute and Xiamen Eye Center, Xiamen University School of Medicine, Fujian, China; and ¶Department of Ophthalmology, Keio University School of Medicine, Tokyo, Japan.
Cornea. 2010 Nov;29 Suppl 1:S32-40. doi: 10.1097/ICO.0b013e3181ea4b13.
Although corneal epithelial stem cells (SCs) are located at the limbus between the cornea and the conjunctiva, not all limbal basal epithelial cells are SCs. Using 2 dispase digestions to remove different amounts of limbal basal epithelial cells for cross-sections, flat mounts, and cytospin preparations, double immunostaining to pancytokeratins (PCK) and vimentin (Vim) identified 3 p63+ epithelial progenitors such as PCK-/Vim+, PCK/Vim, and PCK-/Vim+ and 1 p63+ mesenchymal cell, PCK-/Vim+. PCK-/Vim- progenitors had the smallest cell size were 10-20 times more enriched on collagen I-coated dishes in the 5-minute rapid adherent fraction that contained the highest percentage of p63+ cells but the lowest percentage of cytokeratin12+ cells, and gave rise to high Ki67 labeling and vivid clonal growth. In contrast, PCK+/Vim+ and PCK+/Vim- progenitors were found more in the slow-adherent fraction and yielded poor clonal growth. PCK/Vim progenitors and clusters of PCK-/Vim+ mesenchymal cells, which were neither melanocytes nor Langerhans cells, were located in the limbal basal region. Therefore, differential expression of PCK and Vim helps identify small PCK-/Vim- cells as the most likely candidate for SCs among a hierarchy of heterogeneous limbal basal progenitors, and their close association with PCK-/Vim+ presumed "niche" cells.
虽然角膜上皮干细胞 (SCs) 位于角膜和结膜之间的角膜缘,但并非所有的角膜缘基底上皮细胞都是SCs。通过使用 2 种Dispase 消化来去除不同数量的角膜缘基底上皮细胞进行切片、平片和细胞离心涂片制备,用广谱细胞角蛋白 (PCK) 和波形蛋白 (Vim) 的双重免疫染色鉴定出 3 种 p63+上皮祖细胞,如 PCK-/Vim+、PCK/Vim 和 PCK-/Vim+,以及 1 种 p63+间充质细胞,PCK-/Vim+。PCK-/Vim-祖细胞的细胞体积最小,在含有最高比例 p63+细胞和最低比例细胞角蛋白 12+细胞的 5 分钟快速黏附部分中,在胶原 I 涂层培养皿上的富集度高 10-20 倍,并且具有较高的 Ki67 标记和生动的克隆生长。相比之下,PCK+/Vim+和 PCK+/Vim-祖细胞更多地存在于缓慢黏附部分,产生的克隆生长较差。PCK/Vim 祖细胞和 PCK-/Vim+间充质细胞簇位于角膜缘基底区域,既不是黑素细胞也不是朗格汉斯细胞。因此,PCK 和 Vim 的差异表达有助于将小的 PCK-/Vim-细胞鉴定为异质的角膜缘基底祖细胞中的最有可能的SCs 候选细胞,并且它们与 PCK-/Vim+假定的“龛”细胞密切相关。