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首页> 外文期刊>International journal of oral science >Expression of cellular fibronectin mRNA in adult periodontitis and peri-implantitis: a real-time polymerase chain reaction study
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Expression of cellular fibronectin mRNA in adult periodontitis and peri-implantitis: a real-time polymerase chain reaction study

机译:成人牙周炎和种植体周围炎中细胞纤连蛋白mRNA的表达:实时聚合酶链反应研究

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摘要

Cellular fibronectin (cFn) is a type of bioactive non-collagen glycoprotein regarded as the main substance used to maintain periodontal attachment. The content of cFn in some specific sites can reflect the progress of periodontitis or peri-implantitis. This study aims to evaluate the expression of cFn messenger RNA (mRNA) in tissues of adult periodontitis and peri-implantitis by real-time fluorescent quantitative polymerase chain reaction (PCR) and to determine its clinical significance. A total of 30 patients were divided into three groups of 10: healthy, adult periodontitis and peri-implantitis. Periodontal tissue biopsies (1mm×1mm×1mm) from each patient were frozen in liquid nitrogen. Total RNA was extracted from these tissues, and the content, purity and integrity were detected. Specific primers were designed according to the sequence, and the mRNA expression levels of cellular fibronectin were detected by real-time PCR. The purity and integrity of the extracted total RNA were both high, and the specificity of amplified genes was very high with no other pollution. The mRNA expression of cFn in the adult periodontitis group (1.526±0.441) was lower than that in the healthy group (3.253±0.736). However, the mRNA expression of cFn in the peri-implantitis group (3.965±0.537) was significantly higher than that in the healthy group. The difference revealed that although both processes were destructive inflammatory reactions in the periodontium, the pathomechanisms were different and the variation started from the transcription level of the cFn gene.
机译:细胞纤连蛋白(cFn)是一种具有生物活性的非胶原糖蛋白,被认为是维持牙周附着的主要物质。某些特定部位的cFn含量可反映牙周炎或种植体周围炎的进展。本研究旨在通过实时荧光定量聚合酶链反应(PCR)评估成人牙周炎和种植体周围组织中cFn信使RNA(mRNA)的表达,并确定其临床意义。将总共​​30例患者分为三组,每组10例:健康,成人牙周炎和种植体周围炎。将每个患者的牙周组织活检(1mm×1mm×1mm)冷冻在液氮中。从这些组织中提取总RNA,并检测其含量,纯度和完整性。根据序列设计特异性引物,并通过实时荧光定量PCR检测细胞纤连蛋白的mRNA表达水平。提取的总RNA的纯度和完整性都很高,并且扩增的基因的特异性非常高,没有其他污染。成人牙周炎组cFn的mRNA表达(1.526±0.441)低于健康组(3.253±0.736)。然而,种植体周围炎组中cFn的mRNA表达(3.965±0.537)显着高于健康组。差异表明,尽管这两个过程都是牙周组织的破坏性炎症反应,但其发病机理不同,并且变异始于cFn基因的转录水平。

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