Li D Q, Meller D, Liu Y, Tseng S C
Ocular Surface and Tear Center, Department of Ophthalmology, Bascom Palmer Eye Institute, Miami, Florida, USA.
Invest Ophthalmol Vis Sci. 2000 Feb;41(2):404-10.
To determine whether conjunctivochalasis, denoting redundant, loose, nonedematous inferior bulbar conjunctiva, is associated with increased expression and activity of matrix metalloproteinases (MMPS) over their tissue inhibitors (TIMPs).
Expression of transcripts and proteins of MMPs, TIMPs, and urokinase plasminogen activator (uPA) by cultured normal human conjunctival and conjunctivochalasis fibroblasts was determined by Northern hybridization, enzyme-linked immunosorbent assay (ELISA), and Western blot analysis, respectively. Gelatin and casein zymography and quantitative collagenase activity assay were performed in the serum-free conditioned media.
Compared with normal conjunctival fibroblasts from six subjects, conjunctivochalasis fibroblasts from eight patients showed markedly increased transcript expression of MMP-1 (5- to 32-fold) and MMP-3 (4 to 30-fold), whereas that of MMP-2, TIMP-1, TIMP-2, and uPA was similar between the two groups. Protein levels were increased in the serum-free conditioned media of conjunctivochalasis fibroblasts for MMP-1 (3.5- to 7.6-fold) and MMP-3 (2.3- to 13-fold), determined by ELISA and Western blot analysis. There was increased caseinolytic activity of MMP-3 and collagenolytic activity of MMP-1 (2.2-fold) by conjunctivochalasis fibroblasts, whereas no difference was noted between these two types of fibroblasts in the protein and gelatinolytic activity of MMP-2 or expression of TIMP-1 and TIMP-2 proteins, although that of TIMP-1 transcript was slightly higher in some conjunctivochalasis fibroblasts. No expression of MMP-9 was detected.
Overexpression of MMP-1 and MMP-3 mRNA by conjunctivochalasis fibroblasts is correlated with their increased protein levels and proteolytic activities. Collectively, these data help explain how conjunctivochalasis manifests excessive degradation of the conjunctival matrix and Tenon's capsule.
确定结膜松弛症(表现为球结膜下多余、松弛且无水肿)是否与基质金属蛋白酶(MMPs)相对于其组织抑制剂(TIMPs)的表达增加及活性增强有关。
分别通过Northern杂交、酶联免疫吸附测定(ELISA)及蛋白质印迹分析,测定培养的正常人结膜及结膜松弛症成纤维细胞中MMPs、TIMPs及尿激酶型纤溶酶原激活剂(uPA)的转录本和蛋白表达。在无血清条件培养基中进行明胶和酪蛋白酶谱分析及定量胶原酶活性测定。
与6名受试者的正常结膜成纤维细胞相比,8例患者的结膜松弛症成纤维细胞显示MMP-1(5至32倍)和MMP-3(4至30倍)的转录本表达显著增加,而两组间MMP-2、TIMP-1、TIMP-2及uPA的表达相似。通过ELISA和蛋白质印迹分析确定,结膜松弛症成纤维细胞的无血清条件培养基中MMP-1(3.5至7.6倍)和MMP-3(2.3至13倍)的蛋白水平升高。结膜松弛症成纤维细胞的MMP-3酪蛋白溶解活性和MMP-1胶原溶解活性增加(2.2倍),而在这两种类型的成纤维细胞中,MMP-2的蛋白和明胶溶解活性或TIMP-1及TIMP-2蛋白表达无差异,尽管在一些结膜松弛症成纤维细胞中TIMP-1转录本略高。未检测到MMP-9的表达。
结膜松弛症成纤维细胞中MMP-1和MMP-3 mRNA的过表达与其蛋白水平和蛋白水解活性的增加相关。总体而言,这些数据有助于解释结膜松弛症如何表现为结膜基质和Tenon囊的过度降解。