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首页> 外文期刊>Journal of periodontal research >Expression of matrix metalloproteinase-1, matrix metalloproteinase-2 and extracellular metalloproteinase inducer in human periodontal ligament cells stimulated with interleukin-1 beta.
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Expression of matrix metalloproteinase-1, matrix metalloproteinase-2 and extracellular metalloproteinase inducer in human periodontal ligament cells stimulated with interleukin-1 beta.

机译:白细胞介素-1β刺激人牙周膜细胞中基质金属蛋白酶-1,基质金属蛋白酶-2和细胞外金属蛋白酶诱导剂的表达。

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BACKGROUND AND OBJECTIVES: Matrix metalloproteinases (MMPs), produced by both infiltrating and resident cells of the periodontium, play important roles in physiologic and pathologic events. Both interleukin-1 beta and extracellular MMP inducer can stimulate the expression of MMPs, which in turn leads to breakdown of the periodontium. However, it is currently unknown whether interleukin-1 beta up-regulates MMPs through stimulating the expression of extracellular MMP inducer. The aims of this study were to investigate the effect of interleukin-1 beta on the expression of MMP-1, MMP-2 and extracellular MMP inducer in human periodontal ligament cells and to evaluate whether the regulation of MMP-1 and MMP-2 by this cytokine occurred through an effect on extracellular MMP inducer expression. MATERIAL AND METHODS: Cultured human periodontal ligament cells were treated with varying concentrations (0.01-10 ng/mL) of interleukin-1 beta at for 6, 12 and 24 h. Reverse transcription-polymerase chain reaction, enzyme-linked immunosorbent assay, gelatin zymography and western blotting were performed to measure the mRNA and protein levels of MMP-1, MMP-2 and extracellular MMP inducer. RESULTS: Basal levels of mRNA and protein for MMP-1, MMP-2 and extracellular MMP inducer were detected in untreated human periodontal ligament cells. Interleukin-1 beta significantly up-regulated the expression of MMP-1 and MMP-2 mRNA and protein (p < 0.05); however, the levels of mRNA and protein for extracellular MMP inducer were not significantly different (p > 0.05). In the culture medium, the concentration of MMP-1 was also increased significantly, but the concentration of MMP-1 was not related to the concentration of extracellular MMP inducer (R(2) = 0.2538, p > 0.05). CONCLUSION: Interleukin-1 beta up-regulated the levels of MMP-1 and MMP-2, but it did not alter the expression of extracellular MMP inducer. Expression of MMP-1 and MMP-2 might be elevated by interleukin-1 beta and extracellular MMP inducer via two different signal pathways.
机译:背景与目的:牙周组织浸润和驻留细胞产生的基质金属蛋白酶(MMP)在生理和病理事件中起重要作用。 IL-1β和细胞外MMP诱导剂均可刺激MMP的表达,进而导致牙周膜的破坏。但是,目前尚不清楚白介素-1β是否通过刺激细胞外MMP诱导物的表达来上调MMP。这项研究的目的是调查白细胞介素-1β对人牙周膜细胞中MMP-1,MMP-2和细胞外MMP诱导剂表达的影响,并评估是否通过下列方式调节MMP-1和MMP-2:这种细胞因子通过影响细胞外MMP诱导物表达而发生。材料与方法:将培养的人牙周膜细胞在6、12和24 h内以不同浓度(0.01-10 ng / mL)的白细胞介素1β处理。进行逆转录-聚合酶链反应,酶联免疫吸附试验,明胶酶谱分析和蛋白质印迹分析,以检测MMP-1,MMP-2和细胞外MMP诱导剂的mRNA和蛋白水平。结果:未处理的人牙周膜细胞中MMP-1,MMP-2和细胞外MMP诱导物的mRNA和蛋白质的基础水平被检测到。白介素-1β明显上调MMP-1和MMP-2 mRNA和蛋白的表达(p <0.05);然而,细胞外MMP诱导剂的mRNA和蛋白质水平没有显着差异(p> 0.05)。在培养基中,MMP-1的浓度也显着增加,但MMP-1的浓度与细胞外MMP诱导剂的浓度无关(R(2)= 0.2538,p> 0.05)。结论:白介素-1β上调了MMP-1和MMP-2的水平,但并未改变细胞外MMP诱导剂的表达。白介素-1β和细胞外MMP诱导剂可能通过两种不同的信号途径提高MMP-1和MMP-2的表达。

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