Flaum Eye Institute, University of Rochester Medical Center, Rochester, New York, USA.
Invest Ophthalmol Vis Sci. 2010 Apr;51(4):1935-42. doi: 10.1167/iovs.09-3823. Epub 2009 Nov 11.
Purpose. To characterize phenotypic differences between anterior and posterior corneal keratocytes after stimulation with the profibrotic agent transforming growth factor-beta1 (TGF-beta1) in vitro. Methods. Sixteen corneas from healthy felines were obtained immediately after death. Lamellar dissection was performed to separate the anterior and posterior stroma at approximately 50% depth either manually (n = 2) or with a Moria microkeratome (300-mum head; n = 14). Cells from the anterior and posterior stroma were cultured separately but under identical conditions. Using immunohistochemistry and Western blot techniques, Ki-67 staining and relative expression of Thy-1, alpha smooth muscle actin (alpha-SMA), and fibronectin were assessed after stimulation with different TGF-beta1 concentrations. In addition, anterior and posterior cells cultured in different concentrations of TGF-beta1 were wounded with a razor blade, and the wound area and time to closure were determined. Results. Stimulation by all concentrations of TGF-beta1 increased the proportion of Ki-67-positive cells in anterior and posterior cell cultures, but this increase was noted earlier in posterior cells than in anterior cells. Increasing TGF-beta1 concentration also increased the relative expression of Thy-1, alpha-SMA, and fibronectin in anterior and posterior fibroblasts. However, anterior cells expressed these fibrotic markers at lower TGF-beta1 concentrations than did posterior keratocytes. After mechanical wounding, posterior cells closed the wound area faster than did anterior cells at all concentrations of TGF-beta1. Conclusions. The present experiments show that anterior and posterior corneal keratocytes exhibit different sensitivities to the profibrotic growth factor TGF-beta1. This heterogeneity of keratocyte response may impact wound closure after mechanical wounding.
目的。体外研究转化生长因子-β1(TGF-β1)刺激前后角膜基质成纤维细胞表型差异,以阐明其特征。方法。16 只健康猫死后立即获得角膜。通过手动(n = 2)或 Moria 微型角膜刀(300 微米刀头;n = 14)将角膜分为前后基质层,深度约为 50%。分别对前、后基质层细胞进行培养,但培养条件相同。通过免疫组织化学和 Western blot 技术,检测 Ki-67 染色和 Thy-1、α平滑肌肌动蛋白(α-SMA)和纤维连接蛋白的相对表达,以评估不同 TGF-β1 浓度的刺激作用。此外,用刀片对培养于不同 TGF-β1 浓度的前、后基质层细胞进行划痕实验,测定划痕面积和愈合时间。结果。所有 TGF-β1 浓度刺激均增加了前、后基质层细胞 Ki-67 阳性细胞的比例,但在后基质层细胞中比在前基质层细胞中更早出现。增加 TGF-β1 浓度也增加了前、后角膜基质成纤维细胞中 Thy-1、α-SMA 和纤维连接蛋白的相对表达。然而,前基质层细胞在较低浓度的 TGF-β1 下表达这些纤维化标志物的水平高于后角膜基质细胞。机械划伤后,在后基质层细胞在所有 TGF-β1 浓度下的伤口愈合速度均快于前基质层细胞。结论。本实验表明,前、后角膜基质成纤维细胞对促纤维化生长因子 TGF-β1 的敏感性不同。这种角膜成纤维细胞反应的异质性可能影响机械损伤后的伤口愈合。