Ma D H, Tsai R J, Chu W K, Kao C H, Chen J K
Department of Ophthalmology, Change Gung Memorial Hospital, Tao-Yuan, Taiwan, Republic of China.
Invest Ophthalmol Vis Sci. 1999 Jul;40(8):1822-8.
To study the in vitro angiogenic activity of human conjunctival and limbal epithelial cells and conjunctival, limbal, and corneal fibroblasts in a three-cell-type coculture model.
Human umbilical vein endothelial cells (EC) were cocultured with epithelial cells, fibroblasts, or epithelial cells and fibroblasts to test their effect on EC morphogenesis. Neutralizing antibodies to some known angiogenic factors were added to the culture to see whether the EC morphogenesis may be blocked by a particular antibody.
Conjunctival and limbal epithelial cells exhibited very little or no stimulatory effect on EC tube formation when examined in an EC- epithelial cell coculture system. In contrast, conjunctival, limbal, and corneal fibroblasts all promoted EC morphogenesis when examined under the same culture conditions. Fibroblast-induced EC morphogenesis was inhibited by addition of anti-vascular endothelial growth factor (VEGF) and/or anti-basic fibroblast growth factor (bFGF) antibodies to the culture medium. In the three-cell-type coculture system consisting of ECs, fibroblasts, and epithelial cells, limbal epithelial cells (but not conjunctival epithelial cells) exhibited a strong inhibitory effect on fibroblast-induced EC tube formation.
The proangiogenic activity of ocular surface fibroblasts is probably mediated through a paracrine mechanism by VEGF and bFGF. Limbal epithelial cells, but not conjunctival epithelial cells, inhibit fibroblast-stimulated angiogenesis.
在三细胞类型共培养模型中研究人结膜和角膜缘上皮细胞以及结膜、角膜缘和角膜成纤维细胞的体外血管生成活性。
将人脐静脉内皮细胞(EC)与上皮细胞、成纤维细胞或上皮细胞与成纤维细胞共培养,以测试它们对EC形态发生的影响。向培养物中添加针对一些已知血管生成因子的中和抗体,以观察EC形态发生是否可能被特定抗体阻断。
在EC-上皮细胞共培养系统中检测时,结膜和角膜缘上皮细胞对EC管形成的刺激作用很小或没有。相比之下,在相同培养条件下检测时,结膜、角膜缘和角膜成纤维细胞均促进EC形态发生。向培养基中添加抗血管内皮生长因子(VEGF)和/或抗碱性成纤维细胞生长因子(bFGF)抗体可抑制成纤维细胞诱导的EC形态发生。在由EC、成纤维细胞和上皮细胞组成的三细胞类型共培养系统中,角膜缘上皮细胞(而非结膜上皮细胞)对成纤维细胞诱导的EC管形成表现出强烈的抑制作用。
眼表成纤维细胞的促血管生成活性可能通过VEGF和bFGF的旁分泌机制介导。角膜缘上皮细胞而非结膜上皮细胞抑制成纤维细胞刺激的血管生成。