Foreman D M, Pancholi S, Jarvis-Evans J, McLeod D, Boulton M E
Department of Ophthalmology, University of Manchester, U.K.
Exp Eye Res. 1996 May;62(5):555-64. doi: 10.1006/exer.1996.0065.
The effects of growth factors on re-epithelialization of wounded human and bovine corneas were studied in a simple organ culture system. Excisional trephine and epithelial scrape wounds were created on bovine and human corneo-scleral rings in which the endothelial corneal concavity was then filled with an agar-collagen mixture. Organ culture was undertaken at 37 degrees C in a humidified 5% CO2 incubator with serum-free Medium 199 maintained at the level of the conjunctival epithelium. Rates of reepithelialization in response to addition of exogenous epidermal growth factor (EGF), basic fibroblast growth factor (bFGF) and transforming growth factor type beta 1 (TGF-beta 1) were assessed by image analysis. Corneal cultures could be maintained for up to 3 weeks without significant stromal oedema or keratocyte deterioration and with little loss of epithelial architecture. Following wounding the cornea reepithelialized in a similar fashion to that observed in vivo i.e. a lag phase followed by migration/proliferation and the reformation of an intact multilayered epithelium. EGF accelerated, basic FGF had no effect on, and TGF-beta 1 inhibited the rate of corneal re-epithelialization. Our organ culture model maintains corneal integrity and provides a practical system in which to study factors that modulate corneal reepithelialization following wounding.
在一个简单的器官培养系统中,研究了生长因子对人及牛角膜伤口再上皮化的影响。在牛和人角膜巩膜环上制作切除性环钻伤和上皮刮伤,然后在内皮角膜凹面填充琼脂 - 胶原混合物。在37℃的湿度为5%二氧化碳的培养箱中进行器官培养,用无血清的199培养基维持在结膜上皮水平。通过图像分析评估添加外源性表皮生长因子(EGF)、碱性成纤维细胞生长因子(bFGF)和转化生长因子β1(TGF-β1)后再上皮化的速率。角膜培养物可维持长达3周,无明显基质水肿或角膜细胞恶化,上皮结构几乎无损失。受伤后,角膜再上皮化的方式与体内观察到的相似,即有一个延迟期,随后是迁移/增殖以及完整多层上皮的重新形成。EGF加速了角膜再上皮化,碱性FGF无影响,而TGF-β1抑制了角膜再上皮化的速率。我们的器官培养模型维持了角膜的完整性,并提供了一个实用的系统来研究调节受伤后角膜再上皮化的因素。