*Department of Pharmacology, Israel Institute for Biological Research, Ness Ziona, Israel; and †Cell and Molecular Biology, USAMRICD, Aberdeen Proving Ground, MD.
Cornea. 2014 Jan;33(1):65-71. doi: 10.1097/ICO.0000000000000002.
Limbal epithelial sheets are used to promote corneal surface reconstruction after the detection of limbal epithelial stem cell deficiency. The aim of this study was to evaluate a novel combination of limbal stem cells (LSCs) maintained on contact lenses (CLs) in the presence of a 3T3 feeder cell layer regarding preservation of stem cell phenotype and the potential use for future in vivo transplantation.
Limbal epithelial cells were isolated from rabbit cornea and cultured with 3T3 cells on CLs. The preservation of LSC phenotype was determined using p63α and ABCG2 immunostaining, whereas epithelial differentiation was evaluated using CK3 and CK19. The colony-forming assay was used to determine the percentage of LSCs in cultures. Finally, CLs seeded with PKH26-labeled LSCs were transferred to rabbit eyes after performing a surgical keratectomy, and the transition and phenotype of labeled cells on the corneal surface were evaluated in whole-mount corneas.
Proliferation of individual limbal cells was observed on CLs with a 3T3 feeder cell layer, showing holoclone formation and retention of viable stem or progenitor cell phenotype. Finally, a higher transition of cultivated cells after a dual sequential CL transplantation to the ocular surface was observed, showing the preservation of the LSC phenotype in the corneal surface.
Limbal cells cultivated on a CL carrier overlaying a 3T3 feeder layer are mitotically active and retain the LSC phenotype. This novel technique of using CLs as a carrier offers an easily manipulable and nonimmunogenic method for transferring LSCs for ocular surface reconstruction in patients with limbal epithelial stem cell deficiency.
在发现角膜缘上皮干细胞缺乏后,使用角膜缘上皮片来促进角膜表面重建。本研究旨在评估一种新型的角膜缘干细胞(LSCs)与接触镜(CL)结合的方法,即在 3T3 饲养细胞层的存在下,用于保存干细胞表型,并为未来的体内移植提供潜在用途。
从兔眼角膜分离角膜缘上皮细胞,并在 CL 上与 3T3 细胞共培养。使用 p63α 和 ABCG2 免疫染色来确定 LSC 表型的保存情况,而上皮分化则通过 CK3 和 CK19 进行评估。使用集落形成实验来确定培养物中 LSCs 的百分比。最后,将用 PKH26 标记的 LSCs 接种到 CL 上,然后在进行手术性角膜切除术之后转移到兔眼中,并在整个角膜上评估标记细胞在角膜表面的迁移和表型。
在具有 3T3 饲养细胞层的 CL 上观察到单个角膜缘细胞的增殖,显示出全克隆形成并保留了有活力的干细胞或祖细胞表型。最终,在将培养的细胞进行双重连续 CL 移植到眼表面后,观察到更高的细胞转化率,表明在角膜表面保留了 LSC 表型。
在 3T3 饲养细胞层覆盖的 CL 载体上培养的角膜缘细胞具有有丝分裂活性并保留了 LSC 表型。这种使用 CL 作为载体的新技术为角膜缘上皮干细胞缺乏症患者的眼表面重建提供了一种易于操作且非免疫原性的 LSCs 转移方法。