Department of Ophthalmology, St. Marianna University School of Medicine, Kawasaki, Kanagawa, Japan.
Cornea. 2010 Apr;29(4):432-8. doi: 10.1097/ICO.0b013e3181b9ffcc.
We previously reported the successful transplantation of corneal epithelium-like cells derived from mouse embryonic stem (ES) cells onto injured mouse cornea. Here, we tested whether nonhuman primate ES cells have ability to differentiate into corneal epithelial cells and whether monkey ES cell-derived corneal epithelium-like cells were applicable for the experimental transplantation to damaged cornea.
Monkey ES cells were cultivated on type IV collagen-coated dishes for various days to induce differentiation into corneal epithelium-like cells. The differentiation was evaluated by reverse transcription-polymerase chain reaction and immunostaining. The corneal epithelium-like cells were transplanted to the injured mouse cornea. Reconstitution of the corneal epithelium was evaluated by immunostaining.
The cells cultured on type IV collagen showed cobblestone-like appearance resembling epithelial cells. They expressed messenger RNA of pax6, p63, E-cadherin, CD44, proliferating cell nuclear antigen, keratin 3, and keratin 12. Protein expressions of pax6, keratin 3/12, p63, proliferating cell nuclear antigen, E-cadherin, and CD44 were confirmed by immunostaining. When the corneal epithelium-like cells were transplanted, they adhered to the corneal stroma, leading to formation of multiple cell layers. The grafted cells were stained with anti-human nuclear protein antibody, which cross-reacted with nuclei of monkey cells but not with those of mouse cells. They retained the expressions of keratin 3/12, E-cadherin, and CD44.
We induced corneal epithelium-like cells from monkey ES cells with moderate efficiency. The cells were successfully transplanted onto the injured mouse cornea. This is the first demonstration that nonhuman primate ES cells were induced to differentiate into corneal epithelium-like cells, which were applicable for transplantation to an animal model of corneal injury.
我们之前报道了成功地将源自小鼠胚胎干细胞(ES 细胞)的角膜上皮样细胞移植到受损的小鼠角膜上。在这里,我们测试了非人类灵长类 ES 细胞是否具有分化为角膜上皮细胞的能力,以及猴 ES 细胞衍生的角膜上皮样细胞是否适用于受损角膜的实验性移植。
将猴 ES 细胞在 IV 型胶原包被的培养皿中培养数天,以诱导其分化为角膜上皮样细胞。通过逆转录聚合酶链反应和免疫染色评估分化情况。将角膜上皮样细胞移植到受损的小鼠角膜上。通过免疫染色评估角膜上皮的重建情况。
在 IV 型胶原上培养的细胞呈现出鹅卵石样外观,类似于上皮细胞。它们表达 pax6、p63、E-钙黏蛋白、CD44、增殖细胞核抗原、角蛋白 3 和角蛋白 12 的信使 RNA。通过免疫染色证实了 pax6、角蛋白 3/12、p63、增殖细胞核抗原、E-钙黏蛋白和 CD44 的蛋白表达。当移植角膜上皮样细胞时,它们附着在角膜基质上,形成多个细胞层。移植的细胞被抗人核蛋白抗体染色,该抗体与猴细胞的核反应,但与鼠细胞的核不反应。它们保留了角蛋白 3/12、E-钙黏蛋白和 CD44 的表达。
我们从中诱导出具有中等效率的猴 ES 细胞角膜上皮样细胞。这些细胞成功地移植到受损的小鼠角膜上。这是首次证明非人类灵长类 ES 细胞被诱导分化为角膜上皮样细胞,可适用于动物角膜损伤模型的移植。