Liu L, Hartwig D, Harloff S, Herminghaus P, Wedel T, Geerling G
Department of Ophthalmology, University of Lübeck, Ratzeburger Allee 160, 23538 Lübeck, Germany.
Graefes Arch Clin Exp Ophthalmol. 2005 Jul;243(7):706-14. doi: 10.1007/s00417-004-1106-5. Epub 2005 Mar 9.
Serum eyedrops have been successfully used in the treatment of severe dry eye, persistent epithelial defects and other severe ocular surface disorders. A number of clinical studies showed a variable efficacy of this approach, but the parameters for the production of this blood product varied significantly. In order to establish an optimised protocol for the production of serum eyedrops, we examined the effect of various clotting times, centrifugation forces, types of diluent and dilutions on the concentration of growth factors, fibronectin, and vitamins in serum and tested the epitheliotrophic capacity of these serum modifications in a cell culture model of human SV-40-immortalised corneal epithelial cells (HCE-T).
Serum samples were prepared with a clotting time of 20, 60 or 120 min, a centrifugation force of 500 xg or 3,000 xg, and diluted with BSS or isotonic saline. The concentrations of EGF, TGF-beta1, PDGF-AB, FGF, HGF, fibronectin, vitamin A and vitamin E in these samples were evaluated with ELISA and HPLC. HCE-T cells were incubated for 24, 48, 72, 96 and 144 h with 100, 50, 25, 12.5, 6.25 and 3.125% serum in diluent, and cell proliferation, migration and differentiation were evaluated by means of a luminescence-based ATP assay, a colony-dispersion assay and scanning electron microscopy.
Using a longer clotting time resulted in an increased concentration of all the epitheliotrophic factors examined in serum; the difference was statistically significant for EGF, TGF-beta1 and HGF. Increasing the g force of centrifugation from 500 xg to 3,000 xg resulted in significantly less TGF-beta1, but more EGF and vitamin A. Cell proliferation was better supported by serum prepared with 3,000 xg and diluted with BSS. Serum prepared with a longer clotting time yielded better cell migration and differentiation.
Clotting time, centrifugation and diluents have a significant impact on the composition and epitheliotrophic effects of serum. A long clotting time (>or=120 min), a sharp centrifugation (3,000 xg for 15 min) and dilution with BSS improve the ability of serum eyedrops to support proliferation, migration and differentiation of corneal epithelial cells.
血清滴眼液已成功用于治疗严重干眼症、持续性上皮缺损及其他严重眼表疾病。多项临床研究表明该方法疗效各异,且这种血液制品的制备参数差异显著。为建立血清滴眼液的优化制备方案,我们研究了不同凝血时间、离心力、稀释剂类型及稀释度对血清中生长因子、纤连蛋白和维生素浓度的影响,并在人SV - 40永生化角膜上皮细胞(HCE - T)的细胞培养模型中测试了这些血清制剂的促上皮生长能力。
制备凝血时间为20、60或120分钟、离心力为500×g或3000×g的血清样本,并用平衡盐溶液(BSS)或等渗盐水进行稀释。采用酶联免疫吸附测定(ELISA)和高效液相色谱法(HPLC)评估这些样本中表皮生长因子(EGF)、转化生长因子 - β1(TGF - β1)、血小板衍生生长因子AB(PDGF - AB)、成纤维细胞生长因子(FGF)、肝细胞生长因子(HGF)、纤连蛋白、维生素A和维生素E的浓度。将HCE - T细胞与稀释剂中100%、50%、25%、12.5%、6.25%和3.125%的血清孵育24、48、72、96和144小时,通过基于发光的ATP测定、集落分散测定和扫描电子显微镜评估细胞增殖、迁移和分化。
延长凝血时间会使血清中所有检测的促上皮生长因子浓度增加;表皮生长因子、转化生长因子 - β1和肝细胞生长因子的差异具有统计学意义。将离心力从500×g增加到3000×g会使转化生长因子 - β1显著减少,但表皮生长因子和维生素A增加。用3000×g离心并以BSS稀释制备的血清对细胞增殖的支持更好。凝血时间较长的血清制剂可产生更好的细胞迁移和分化。
凝血时间、离心和稀释剂对血清的成分和促上皮生长作用有显著影响。较长的凝血时间(≥120分钟)、高速离心(3000×g离心15分钟)和用BSS稀释可提高血清滴眼液支持角膜上皮细胞增殖、迁移和分化的能力。