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首页> 外文期刊>Journal of glaucoma >Matrix metalloproteinases and their tissue inhibitors in aqueous humor of patients with primary open-angle glaucoma, exfoliation syndrome, and exfoliation glaucoma.
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Matrix metalloproteinases and their tissue inhibitors in aqueous humor of patients with primary open-angle glaucoma, exfoliation syndrome, and exfoliation glaucoma.

机译:原发性开角型青光眼,剥脱综合征和剥脱性青光眼患者房水中的基质金属蛋白酶及其组织抑制剂。

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PURPOSE: To study extracellular matrix (ECM) metabolism by matrix metalloproteinases (MMPs) and their tissue inhibitors (TIMPs) in aqueous humor (AH) samples collected from primary open-angle glaucoma (POAG), exfoliation syndrome (EXS), and exfoliation glaucoma (EXG) in relation to samples derived from cataract control patients. MATERIALS AND METHODS: Seventy-one AH samples were collected during cataract extraction and trabeculectomy. The expression and molecular forms of MMP-2, -8, -9, -13, and -14 and tissue inhibitor of metalloproteinases-1 and -2 (TIMPs) were analyzed by Western immunoblotting. Gelatinase and collagenase activities were studied by zymography and type I collagen degradation assays, respectively. MMP-2 and TIMP-2 concentrations were measured by ELISA assays. RESULTS: By Western immunoblotting all the studied MMPs were mainly in their latent form in all diagnostic groups. Zymography demonstrated that MMP-2 represents the major gelatinase in AH. Similarly, type I collagenolytic activity was low and similar in cataract and glaucoma samples. In ELISA measurements the TIMP-2 levels were significantly elevated in glaucoma and EXS samples in comparison to cataract controls (P < 0.05). CONCLUSION: TIMP-2 is elevated in glaucomatous process over MMP-2, which support and further extend the conjuncture that the ECM accumulation rather than degradation predominates in the pathogenesis of POAG and EXG.
机译:目的:研究从原发性开角型青光眼(POAG),剥脱综合征(EXS)和剥脱性青光眼收集的房水(AH)样本中基质金属蛋白酶(MMPs)及其组织抑制剂(TIMPs)的细胞外基质(ECM)代谢(EXG)与白内障对照患者的样本有关。材料与方法:在白内障摘除和小梁切除术中收集了71个AH样本。通过Western免疫印迹分析了MMP-2,-8,-9,-13和-14以及金属蛋白酶-1和-2(TIMPs)的组织抑制剂的表达和分子形式。明胶酶和胶原酶的活性分别通过酶谱和I型胶原降解试验进行了研究。通过ELISA测定法测量MMP-2和TIMP-2的浓度。结果:通过Western免疫印迹,所有诊断组中所有研究的MMP均以潜伏形式存在。 Zymography显示MMP-2代表AH中的主要明胶酶。类似地,在白内障和青光眼样品中,I型胶原蛋白水解活性较低且相似。在ELISA测量中,与白内障对照组相比,青光眼和EXS样品中的TIMP-2水平显着升高(P <0.05)。结论:青光眼过程中TIMP-2的表达高于MMP-2,这支持并进一步扩展了在POAG和EXG发病机理中ECM积累而非降解占主导地位的假设。

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