Research Unit for Rare Diseases, Clinic of Paediatrics and Adolescent Medicine, 1st Faculty of Medicine, Charles University, Ke Karlovu 2, 128 08 Prague 2, Czech Republic; Laboratory of the Biology and Pathology of the Eye, Institute of Biology and Medical Genetics, 1st Faculty of Medicine, Charles University and General University Hospital in Prague, Albertov 4, 128 00 Prague 2, Czech Republic.
Laboratory of the Biology and Pathology of the Eye, Institute of Biology and Medical Genetics, 1st Faculty of Medicine, Charles University and General University Hospital in Prague, Albertov 4, 128 00 Prague 2, Czech Republic.
Exp Eye Res. 2018 Nov;176:20-28. doi: 10.1016/j.exer.2018.06.019. Epub 2018 Jun 19.
Human limbal epithelial cells (LECs) intended for treatment of limbal stem cell deficiency are commonly cultivated on a 3T3 feeder layer with complex culture medium supplemented with fetal bovine serum (FBS). However, FBS is a xenogeneic component containing poorly characterised constituents and exhibits quantitative and qualitative lot-to-lot variations. Human limbal explants were plated on untreated or fibrin coated plastic plates and cultured in two non-xenogeneic media (supplemented with either human serum or platelet lysate only). Our aim was to find out whether the characteristics of harvested LEC cultures are comparable to those of LEC cultivated in the gold standard - FBS-supplemented complex medium. The growth kinetics, cell proliferation, differentiation, stemness maintenance, apoptosis and contamination by other cell types were evaluated and compared among these conditions. In all of them LECs were successfully cultivated. Stemness was preserved in both xeno-free media. However, cells cultured with human serum on the fibrin-coated plates had the highest growth rate and cell proliferation and very low fibroblast-like cell contamination. These data suggest that xeno-free cell culture conditions can replace the traditional FBS-supplemented medium and thereby provide a safer protocol for ex vivo cultured limbal stem cell transplants.
用于治疗角膜缘干细胞缺陷的人角膜缘上皮细胞(LEC)通常在 3T3 饲养层上培养,并用含有胎牛血清(FBS)的复杂培养基进行补充。然而,FBS 是一种异种成分,含有特征不明确的成分,并且表现出定量和定性的批间变化。人角膜缘外植体被种植在未经处理或纤维蛋白涂层的塑料板上,并在两种非异种(xenogeneic)培养基(仅用人血清或血小板裂解物补充)中培养。我们的目的是了解在金标准 - FBS 补充的复杂培养基中培养的 LEC 与在不含异种成分的培养基中培养的 LEC 的特征是否可比。在这些条件下评估和比较了收获的 LEC 培养物的生长动力学、细胞增殖、分化、干细胞维持、细胞凋亡和被其他细胞类型污染的特征。在所有这些条件下,LEC 都被成功培养。在两种无异种成分的培养基中都保留了干细胞特性。然而,在纤维蛋白涂层板上用人血清培养的细胞具有最高的生长速度和细胞增殖,并且成纤维细胞样细胞污染非常低。这些数据表明,无异种成分的细胞培养条件可以替代传统的 FBS 补充培养基,从而为体外培养的角膜缘干细胞移植提供更安全的方案。