首页> 外文期刊>Ophthalmic Research: Journal for Research in Experimental and Clinical Ophthalmology >Expression of matrix metalloproteinases in wound healing after glaucoma filtration surgery in rabbits.
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Expression of matrix metalloproteinases in wound healing after glaucoma filtration surgery in rabbits.

机译:兔青光眼滤过术后伤口愈合中基质金属蛋白酶的表达

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PURPOSE: To investigate the protein and mRNA expressions of matrix metalloproteinases (MMPs), gelatinolytic activity and localization of MMP activity in wounds after glaucoma filtration surgery in rabbits. METHODS: Sixty eyes of 30 rabbits were removed 1, 3, 7, 14 and 120 days after the surgery and used for this experiment. Protein and mRNA expressions were analyzed by immunohistochemistry and laser capture microdissection/real-time RT-PCR, respectively. The gelatinolytic activity was analyzed by gelatin zymography and the localization was studied using in situ zymography. RESULTS: By immunohistochemistry, expression of MMP-1, MMP-2, MMP-3, MMP-9 and MT1-MMP was detected in the wounds, most markedly 3 days after the surgery. MMP-positive cells were predominantly macrophages. Expression of MMP-9 and MT1-MMP mRNAs was verified by RT-PCR. Gelatinolytic activities corresponding to proMMP-2 and the active form of MMP-2 were detected in the wounds 3 and 7 days after surgery. In situ zymography localized gelatinolytic activities at the wound site. These activities were almost completely abolished by an MMP inhibitor, indicating that the gelatinolytic activity belongs to metalloproteinases. CONCLUSIONS: MMPs, particularly MMP-2/MT1-MMP, play important roles in the degradation of the extracellular matrix in the wound healing process after glaucoma filtration surgery and may represent an important target for therapeutic intervention after glaucoma filtration surgery.
机译:目的:探讨青光眼滤过手术后伤口中基质金属蛋白酶(MMPs)的蛋白和mRNA表达,明胶分解活性和MMP活性的定位。方法:在手术后1、3、7、14和120天摘除30只兔的60只眼,用于本实验。分别通过免疫组织化学和激光捕获显微切割/实时RT-PCR分析蛋白质和mRNA的表达。通过明胶酶谱分析明胶分解活性,并使用原位酶谱研究其定位。结果:通过免疫组织化学方法,在手术后3天发现伤口中MMP-1,MMP-2,MMP-3,MMP-9和MT1-MMP的表达。 MMP阳性细胞主要是巨噬细胞。通过RT-PCR验证MMP-9和MT1-MMP mRNA的表达。术后3和7天,在伤口中检测到与proMMP-2和活性形式的MMP-2相对应的明胶分解活性。原位酶谱分析在伤口部位的明胶分解活性。 MMP抑制剂几乎完全消除了这些活性,表明明胶分解活性属于金属蛋白酶。结论:MMP,尤其是MMP-2 / MT1-MMP,在青光眼滤过术后伤口愈合过程中在细胞外基质降解中起重要作用,并且可能代表青光眼滤过术后治疗干预的重要目标。

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