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首页> 外文期刊>BMC Ophthalmology >Expression of matrix Metalloproteinases-2 and aquaporin-1 in corneoscleral junction after angle-closure in rabbits
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Expression of matrix Metalloproteinases-2 and aquaporin-1 in corneoscleral junction after angle-closure in rabbits

机译:闭角后兔角膜巩膜交界处基质金属蛋白酶2和水通道蛋白1的表达

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To investigate the expression of Matrix Metalloproteinases 2 and aquaporin-1 in corneoscleral junction and explore the mechanism of trabecular damageafter angle-closure. Thirty New Zealand white rabbits were randomly assigned into 2 groups, theexperimental group (Group 1) including twenty five rabbits and the control group (Group 2) including 5 rabbits. The rabbits in the experimental group were used to establish angle-closure models, and the rabbits in the control group were not subjected to any operation. All the rabbits were followed by slit lamp microscopy, Tonopen tonometer, and anterior segment optical coherent tomography (AS-OCT). The expressions of metalloproteinase MMP-2, aquaporin-1, and tissue inhibitors of metalloproteinase-2 in corneoscleral junctionwere evaluatedin both groups byimmunofluorescence, quantitative reverse-transcription polymerase chain reaction (qRT-PCR), and enzyme-linked immunosorbent assay (ELISA). Slit-lamp examination showed that angle-closure model was successfully established in twenty rabbits. The extent of angle-closure was about 2 to 4 clock hours in all the rabbit models, but the intraocular pressure (IOP) of the rabbits distributed from 8.57 to 15.25?mmHg and no significant high IOP was found in the follow-up period. The AQP-1-positive cells mainly located in Schlemm’s canal, the inner surface of trabecular meshwork (TM), and the surface of iris, which began to decline on 1?month after angle-closure. MMP2 staining was diffuse in trabecular meshwork and iris. Immunofluorescence signal of MMP2 was strong within 1?month after angle-closure, and subsequently became weak. qRT-PCR and ELISA showed that the expression of MMP-2 and TIMP-2 increased within 1?month after angle-closure and then declined gradually. The AQP-1 levels showed slightly declined on 1?month after angle-closure. Altered levels of MMPs, TIMPs, and AQP-1 were found in the area of angle-closure, which may be involved in the damage of TM and Schlemm’s canal after angle-closure.
机译:探讨角膜巩膜交界处基质金属蛋白酶2和aquaporin-1的表达,探讨闭角后小梁损伤的机制。新西兰大白兔30只,随机分为2组,实验组(组1)25只,对照组(组2)5只。实验组采用兔子建立闭角模型,对照组不进行任何手术。所有兔均进行裂隙灯显微镜检查,Tonopen眼压计和前节光学相干断层扫描(AS-OCT)。分别通过免疫荧光,定量逆转录聚合酶链反应(qRT-PCR)和酶联免疫吸附测定(ELISA)评估两组在角膜巩膜交界处金属蛋白酶MMP-2,水通道蛋白1和金属蛋白酶2组织抑制剂的表达。裂隙灯检查显示成功建立了20只兔子的闭角模型。在所有兔子模型中,闭角程度约为2至4个时钟小时,但在随访期间,兔子的眼压(IOP)分布在8.57至15.25mmHg之间,并且没有发现明显的高IOP。 AQP-1阳性细胞主要位于施勒姆管,小梁网的内表面和虹膜表面,这些细胞在闭角后1个月开始下降。 MMP2染色弥漫在小梁网和虹膜中。闭角后1个月内MMP2的免疫荧光信号较强,随后减弱。 qRT-PCR和ELISA结果显示,MMP-2和TIMP-2的表达在闭角后1个月内升高,然后逐渐下降。闭角后1个月,AQP-1水平略有下降。在闭角区域发现MMP,TIMP和AQP-1的水平发生变化,这可能与闭角后TM和Schlemm根管的损伤有关。

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