Kim Hyun-Seung, Shang Tieyan, Chen Zhuo, Pflugfelder Stephen C, Li De-Quan
The Ocular Surface Center, Cullen Eye Institute, Department of Ophthalmology, Baylor College of Medicine, 6565 Fannin Street, NC-205, Houston, TX 77030, USA.
Exp Eye Res. 2004 Aug;79(2):263-74. doi: 10.1016/j.exer.2004.05.003.
Matrix metalloproteinases (MMPs) have been implicated in the pathogenesis of ocular surface diseases. This study investigated the regulated expression of gelatinases (MMP-2 and -9), collagenases (MMP-1 and -13) and stromelysins (MMP-3, -10, and -11) by TGF-beta1 in cultured human corneal epithelial cells. Primary human corneal epithelial cell cultures were grown to confluence and treated with different concentrations (0.1, 1.0, 10 ng ml(-1)) of TGF-beta1 in serum-free medium for 6-24 hr. Total RNA was isolated from cultured cells with or without TGF-beta1 treatment for 6 hr and subjected to semi-quantitative RT-PCR and Northern hybridization. Conditioned media were collected from cultures with or without TGF-beta1 treatment for 24 hr to evaluate the MMP production by ELISA and activity assays. Semi-quantitative RT-PCR revealed that the expressions of MMP-9, -1, -13, -3, -10 and -11 mRNA were up-regulated by TGF-beta1 in a concentration-dependent fashion, while MMP-2 and MMP-14 production did not change. Northern hybridization confirmed these findings. Gelatin zymography, MMP ELISA and activity assays showed concentration-dependent stimulated production and activity of MMP-9, -1, -13, -3 and -10 protein in the conditioned media of cultures treated for 24 hr with TGF-beta1. In conclusion, our results demonstrate that TGF-beta1 stimulates the expression and production of gelatinase (MMP-9), collagenases (MMP-1, -13) and stromelysins (MMP-3, -10, -11) in human corneal epithelial cells. These findings suggest that TGF-beta1 may play a role in the pathogenesis of MMP mediated ocular surface diseases, such as sterile corneal ulceration.
基质金属蛋白酶(MMPs)与眼表疾病的发病机制有关。本研究调查了转化生长因子-β1(TGF-β1)对培养的人角膜上皮细胞中明胶酶(MMP-2和-9)、胶原酶(MMP-1和-13)以及基质溶素(MMP-3、-10和-11)表达的调控作用。将原代人角膜上皮细胞培养至汇合状态,然后在无血清培养基中用不同浓度(0.1、1.0、10 ng/ml)的TGF-β1处理6 - 24小时。从经或未经TGF-β1处理6小时的培养细胞中提取总RNA,进行半定量逆转录聚合酶链反应(RT-PCR)和Northern杂交。收集经或未经TGF-β1处理24小时的培养物条件培养基,通过酶联免疫吸附测定(ELISA)和活性测定来评估MMP的产生情况。半定量RT-PCR结果显示,TGF-β1以浓度依赖性方式上调MMP-9、-1、-13、-3、-10和-11 mRNA的表达,而MMP-2和MMP-14的产生没有变化。Northern杂交证实了这些结果。明胶酶谱分析、MMP ELISA和活性测定表明,在用TGF-β1处理24小时的培养物条件培养基中,MMP-9、-1、-13、-3和-10蛋白产生和活性呈浓度依赖性增加。总之,我们的结果表明,TGF-β1刺激人角膜上皮细胞中明胶酶(MMP-9)、胶原酶(MMP-1、-13)和基质溶素(MMP-3、-10、-11)的表达和产生。这些发现提示TGF-β1可能在MMP介导的眼表疾病如无菌性角膜溃疡的发病机制中起作用。