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龈沟液中的表皮生长因子及其在人类炎症性和非炎症性牙龈中的结合能力。

Epidermal growth factor in gingival crevicular fluid and its binding capacity in inflamed and non-inflamed human gingiva.

作者信息

Chang K M, Lehrhaupt N, Lin L M, Feng J, Wu-Wang C Y, Wang S L

机构信息

Department of Periodontics, UMDNJ-New Jersey Dental School, Newark 07103-2400, USA.

出版信息

Arch Oral Biol. 1996 Jul;41(7):719-24. doi: 10.1016/s0003-9969(96)00024-6.

DOI:10.1016/s0003-9969(96)00024-6
PMID:9015575
Abstract

Epidermal growth factor (EGF) is a pro-inflammatory small peptide (6000 Da) with a variety of biological activities including stimulation of cell differentiation and mediation of proteolysis by binding to its specific receptor on the cell surface. The purpose of this study was to determine the levels of EGF in gingival crevicular fluid (GCF) and the EGF-binding capacity to its receptor in gingival tissue. The GCF samples were collected from six patients by inserting paper strips into shallow (< 5 mm) and deep pockets (> or = 5 mm) for 30 s. The strips were soaked in 0.2 M acetate for extraction and the EGF in the supernatants was analysed by radioimmunoassay. To determine the binding capacity of EGF to its receptor, inflamed gingival tissues (pocket depth > or = 5 mm, Gingival Index = 1, 2 or 3) were collected during periodontal flap surgery and non-inflamed gingival tissues (pocket depth < 5 mm, Gingival Index = 0) were collected during surgical "crown lengthening' for aesthetic purposes. The tissues were pooled by group, homogenized for membrane preparation and the supernatants obtained after centrifugation were used in a 125IEGF binding assay. To determine the effect of inflammation on gingival EGF receptor, inflamed and non-inflamed gingival tissues were collected from six patients and prepared similarly to the binding assay. Gingival preparations were then electrophoresed for Western blot analysis with EGF receptor antiserum. The EGF level in GCF was significantly lower (P < 0.05) in the samples collected from pockets > or = 5 mm (0.9 +/- 0.6 ng/ml) than in those from pockets < 5 mm (2.4 +/- 2.1 ng/ml). The average Gingival Index was higher (2.6 +/- 0.6) in pockets > or = 5 mm than in pockets < 5 mm (1.4 +/- 1.0). Specific binding of 125I-EGF to its receptor in inflamed gingiva was 2.7-fold higher than in non-inflamed gingiva (14.4 +/- 4.9 vs 5.4 +/- 1.8 fmol/g wet tissue). Western blot analysis showed two major immunoreactive bands (180 and 120 kDa), which represent EGF receptor and its degradation products, in inflamed gingiva. The findings show that inflammation activates EGF binding capacity in gingiva and that the up-regulation of EGF receptor in inflamed gingiva might be associated with a lowered concentration of EGF in GCF produced adjacent to inflamed gingiva. This up-regulation of EGF receptor during inflammation might be an important mechanism in the pathogenesis of periodontal disease.

摘要

表皮生长因子(EGF)是一种促炎性小肽(6000道尔顿),具有多种生物活性,包括通过与细胞表面的特异性受体结合来刺激细胞分化和介导蛋白水解。本研究的目的是测定龈沟液(GCF)中EGF的水平以及牙龈组织中EGF与其受体的结合能力。通过将纸条插入浅袋(<5毫米)和深袋(≥5毫米)30秒,从6名患者中收集GCF样本。将纸条浸泡在0.2M乙酸盐中进行提取,并用放射免疫分析法分析上清液中的EGF。为了测定EGF与其受体的结合能力,在牙周翻瓣手术期间收集炎症牙龈组织(袋深≥5毫米,牙龈指数=1、2或3),在出于美学目的的手术“牙冠延长术”期间收集非炎症牙龈组织(袋深<5毫米,牙龈指数=0)。将组织按组汇集,匀浆以制备膜,离心后获得的上清液用于125I-EGF结合测定。为了确定炎症对牙龈EGF受体的影响,从6名患者中收集炎症和非炎症牙龈组织,并以与结合测定类似的方式制备。然后将牙龈制剂进行电泳,用EGF受体抗血清进行蛋白质印迹分析。从≥5毫米的袋中收集的样本中GCF中的EGF水平(0.9±0.6纳克/毫升)明显低于从<5毫米的袋中收集的样本(2.4±2.1纳克/毫升)(P<0.05)。≥5毫米的袋中的平均牙龈指数(2.6±0.6)高于<5毫米的袋中的平均牙龈指数(1.4±1.0)。125I-EGF在炎症牙龈中与其受体的特异性结合比在非炎症牙龈中高2.7倍(14.4±4.9对5.4±1.8飞摩尔/克湿组织)。蛋白质印迹分析显示,在炎症牙龈中有两条主要的免疫反应带(180和120千道尔顿),分别代表EGF受体及其降解产物。研究结果表明,炎症激活了牙龈中的EGF结合能力,炎症牙龈中EGF受体的上调可能与炎症牙龈附近产生的GCF中EGF浓度降低有关。炎症期间EGF受体的这种上调可能是牙周病发病机制中的一个重要机制。

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