Covre Joyce Luciana, Loureiro Renata Ruoco, Cristovam Priscila Cardoso, Ricardo José Reinaldo Da Silva, Haapalainen Edna Freymuller, Gomes José Álvaro Pereira
Centro Avançado de Superfície Ocular, Instituto da Visão, Departamento de Oftalmologia, Universidade Federal de São Paulo, SP, Brasil.
Arq Bras Oftalmol. 2011 Mar-Apr;74(2):114-7. doi: 10.1590/s0004-27492011000200009.
To evaluate the efficacy and ultrastructural aspects of human limbal epithelial cells cultured on amniotic membrane (AM) with and without epithelium.
Limbal epithelial cell cultures were established from cadaveric cor neo-scleral rim explants derived from 6 different donors. The explants from each donor were placed under 3 different groups: on human preserved AM with epithelium (Group 1), AM deepithelialized with trypsin (Group 2) and control (Group 3). The epithelial cell migration was evaluated under phase contrast microscopy. After 15 days, the amniotic membrane with cells cultures were removed and submitted to scanning and transmission electron microscopy to check for epithelial migration and adhesion.
All epithelial cell cultures from the controls grew over the botton of the culture plate wells until reaching confluence. Epithelial cultures grew over all but one denuded amniotic membrane. In the group amniotic membrane with epithelium, epithelial cell growing was observed only in 1 well.
Using this model, denuded amniotic membrane appeared to be the best substrate for epithelial cell migration and adhesion comparing to amniotic membrane with epithelium. Removal of amniotic membrane epithelial seems to be an important step for establishing limbal epithelial cell culture on amniotic membrane.
评估在有或无上皮的羊膜(AM)上培养的人角膜缘上皮细胞的疗效及超微结构特征。
从6个不同供体的尸体角膜缘-巩膜缘外植体建立角膜缘上皮细胞培养物。每个供体的外植体被置于3个不同组:有上皮的人保存羊膜上(第1组)、用胰蛋白酶去上皮的羊膜(第2组)和对照组(第3组)。在相差显微镜下评估上皮细胞迁移。15天后,移除带有细胞培养物的羊膜并进行扫描和透射电子显微镜检查以检测上皮迁移和黏附情况。
对照组的所有上皮细胞培养物在培养板孔底部生长直至汇合。上皮培养物在除一张去上皮羊膜外的所有羊膜上生长。在有上皮的羊膜组中,仅在1个孔中观察到上皮细胞生长。
使用该模型,与有上皮的羊膜相比,去上皮羊膜似乎是上皮细胞迁移和黏附的最佳基质。去除羊膜上皮似乎是在羊膜上建立角膜缘上皮细胞培养的重要步骤。