Department of Biomedicine, Unit of Dental Sciences and Biomaterials, University of Trieste, Trieste, Italy.
J Dent Res. 2014 Mar;93(3):263-8. doi: 10.1177/0022034513516465. Epub 2013 Dec 11.
The use of protein cross-linking agents during bonding procedures has been recently proposed to improve bond durability. This study aimed to use zymography and in situ zymography techniques to evaluate the ability of 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide (EDC) cross-linker to inhibit matrix metalloproteinase (MMP) activity. The hypotheses tested were that: (1) bonding procedures increase dentin gelatinolytic activity and (2) EDC pre-treatment prevents this enzymatic activity. The zymographic assay was performed on protein extracts obtained from dentin powder treated with Optibond FL or Scotchbond 1XT with or without 0.3M EDC pre-treatment. For in situ zymography, adhesive/dentin interfaces were created with the same adhesives applied to acid-etched dentin slabs pre-treated or not with EDC conditioner. Zymograms revealed increased expression of dentin endogenous MMP-2 and -9 after adhesive application, while the use of EDC as a primer inactivated dentin gelatinases. Results of in situ zymograpy showed that hybrid layers of tested adhesives exhibited intense collagenolytic activity, while almost no fluorescence signal was detected when specimens were pre-treated with EDC. The correlative analysis used in this study demonstrated that EDC could contribute to inactivate endogenous dentin MMPs within the hybrid layer created by etch-and-rinse adhesives.
近年来,人们提出在黏接程序中使用蛋白质交联剂来提高黏接耐久性。本研究旨在使用组织蛋白酶谱法和原位组织蛋白酶谱法技术来评估 1-乙基-3-(3-二甲基氨基丙基)碳二亚胺(EDC)交联剂抑制基质金属蛋白酶(MMP)活性的能力。测试的假设是:(1)黏接程序会增加牙本质明胶酶活性;(2)EDC 预处理可防止这种酶活性。在经过 Optibond FL 或 Scotchbond 1XT 处理的牙本质粉末的蛋白提取物上进行组织蛋白酶谱分析,其中包括或不包括 0.3M EDC 预处理。对于原位组织蛋白酶谱分析,在经过或未经 EDC 调节剂预处理的酸蚀牙本质片上使用相同的黏接剂来创建黏接/牙本质界面。组织蛋白酶谱显示,黏接剂应用后牙本质内源性 MMP-2 和 -9 的表达增加,而 EDC 用作底漆可使牙本质明胶酶失活。原位组织蛋白酶谱分析的结果表明,所测试的黏接剂的混合层表现出强烈的胶原蛋白酶活性,而当样本用 EDC 预处理时,几乎检测不到荧光信号。本研究中使用的相关分析表明,EDC 可能有助于使酸蚀-冲洗黏接剂形成的混合层中的内源性牙本质 MMP 失活。
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