首页> 美国卫生研究院文献>other >Altered Expression Levels of MMP1 MMP9 MMP12 TIMP1 and IL-1β as a Risk Factor for the Elevated IOP and Optic Nerve Head Damage in the Primary Open-Angle Glaucoma Patients
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Altered Expression Levels of MMP1 MMP9 MMP12 TIMP1 and IL-1β as a Risk Factor for the Elevated IOP and Optic Nerve Head Damage in the Primary Open-Angle Glaucoma Patients

机译:MMP1MMP9MMP12TIMP1和IL-1β的表达水平改变是原发性开角型青光眼患者IOP和视神经头部损害升高的危险因素

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摘要

The aim of presented work was to analyze the impact of particular polymorphic changes in the promoter regions of the -1607 1G/2G MMP1, -1562 C/T MMP9, -82 A/G MMP12, -511 C/T IL-1β, and 372 T/C TIMP1 genes on their expression level in POAG patients. Blood and aqueous humor samples acquired from 50 patients with POAG and 50 control subjects were used for QPCR and protein levels analysis by ELISA. In vivo promoter activity assays were carried on HTM cells using dual luciferase assay. All studied subjects underwent ophthalmic examination, including BCVA, intraocular pressure, slit-lamp examination, gonioscopy, HRT, and OCT scans. Patients with POAG are characterized by an increased mRNA expression of MMP1, MMP9, MMP12, and IL-1β genes as compared to the control group (P < 0.001). Aqueous humor acquired from patients with POAG displayed increased protein expression of MMP1, MMP9, MMP12, and IL-1β compared to the control group (P < 0.001). Allele -1607 1G of MMP1 gene possesses only 42,91% of the -1607 2G allele transcriptional activity and allele -1562 C of MMP9 gene possesses only 21,86% of the -1562 T allele. Increased expression levels of metalloproteinases can be considered as a risk factor for the development of POAG.
机译:提出工作的目的是分析特定多态性变化对-1607 1G / 2G MMP1,-1562 C / T MMP9,-82 A / G MMP12,-511 C / TIL-1β,和372个T / C TIMP1基因在POAG患者中的表达水平。从50例POAG患者和50例对照受试者中采集的血液和房水样本用于QPCR和通过ELISA进行蛋白质水平分析。使用双重荧光素酶测定法在HTM细胞上进行体内启动子活性测定法。所有研究对象均接受了眼科检查,包括BCVA,眼压,裂隙灯检查,斜视镜检查,HRT和OCT扫描。与对照组相比,POAG患者的特征在于MMP1,MMP9,MMP12和IL-1β基因的mRNA表达增加(P <0.001)。与对照组相比,从POAG患者中获得的房水显示出MMP1,MMP9,MMP12和IL-1β的蛋白表达增加(P <0.001)。 MMP1基因的等位基因-1607 1G仅具有-1607 2G等位基因的转录活性的42.91%,MMP9基因的等位基因-1562 C仅具有-1562 T等位基因的21.86%。金属蛋白酶表达水平的增加可以认为是发展POAG的危险因素。

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