首页> 外文期刊>Journal of periodontal research >Alteration in expression of MMP-1 and MMP-2 but not TIMP-1 and TIMP-2 in hereditary gingival fibromatosis is mediated by TGF-beta 1 autocrine stimulation.
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Alteration in expression of MMP-1 and MMP-2 but not TIMP-1 and TIMP-2 in hereditary gingival fibromatosis is mediated by TGF-beta 1 autocrine stimulation.

机译:TGF-β1自分泌刺激介导遗传性牙龈纤维瘤病中MMP-1和MMP-2表达的改变,而不是TIMP-1和TIMP-2的表达改变。

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摘要

Hereditary gingival fibromatosis (HGF) is characterized by an excess accumulation of extracellular matrix (ECM) resulting in a generalized and fibrotic enlargement of the gingiva. To investigate some of the regulatory features of this condition, gingival fibroblasts from normal gingiva (NG) and HGF were examined for the expression and production of matrix metalloproteinases (MMPs) and their inhibitors, tissue matrix metalloproteinases inhibitor (TIMPs). Our results, obtained from 2 different assays, semi-quantitative reverse transcriptase-polymerase chain reaction (RT-PCR) and enzymography, clearly demonstrated that the expression and production of MMP-1 and MMP-2 was significantly lower in fibroblasts from HGF than from NG. Interestingly, TIMP-1 and TIMP-2 expression from NG cells was shown to be slightly higher to those from HGF. Addition of antibodies against transforming growth factor-beta 1 (TGF-beta 1), which is produced in greater amounts by HGF fibroblasts, resulted in a slight increase in MMP-1 and a decrease in MMP-2 expression, whereas TIMP-1 and TIMP-2 expressions were unaffected. These patterns of expression and production suggest that enhanced TGF-beta 1 production reduce the proteolytic activities of HGF fibroblasts, which favor the accumulation of ECM.
机译:遗传性牙龈纤维瘤病(HGF)的特征是细胞外基质(ECM)的过度积累,导致牙龈普遍性和纤维化。为了研究这种疾病的某些调节特征,检查了正常牙龈(NG)和HGF的牙龈成纤维细胞的基质金属蛋白酶(MMP)及其抑制剂,组织基质金属蛋白酶抑制剂(TIMPs)的表达和产生。我们的结果是从2种不同的测定,半定量逆转录酶-聚合酶链反应(RT-PCR)和酶谱学中获得的,清楚地表明,HGF成纤维细胞中MMP-1和MMP-2的表达和产生明显低于HGF。 NG。有趣的是,NG细胞的TIMP-1和TIMP-2表达被证明比HGF的表达略高。 HGF成纤维细胞大量产生的针对转化生长因子β1(TGF-beta 1)的抗体的添加导致MMP-1的轻微增加和MMP-2的表达减少,而TIMP-1和TIMP-2表达不受影响。这些表达和产生的模式表明增强的TGF-β1产生降低了HGF成纤维细胞的蛋白水解活性,这有利于ECM的积累。

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