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首页> 外文期刊>Matrix biology: Journal of the International Society for Matrix Biology >Effect of adenovirus-mediated overexpression of decorin on metalloproteinases, tissue inhibitors of metalloproteinases and cytokines secretion by human gingival fibroblasts.
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Effect of adenovirus-mediated overexpression of decorin on metalloproteinases, tissue inhibitors of metalloproteinases and cytokines secretion by human gingival fibroblasts.

机译:腺病毒介导的decorin过表达对人牙龈成纤维细胞金属蛋白酶,金属蛋白酶组织抑制剂和细胞因子分泌的影响。

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摘要

Decorin is a small leucine-rich proteoglycan that plays a role in control of cell proliferation, cell migration, collagen fibrillogenesis and modulation of the activity of TGF-beta. In the present study, we investigated the effects of decorin on the production of metalloproteinases (MMP-1, -2, -3, -9 and -13), tissue inhibitors of metalloproteinases (TIMP-1, -2) and cytokines (TGF-beta, IL-1beta, IL-4 and TNF-alpha). Decorin was overexpressed in cultured human gingival fibroblasts using adenovirus-mediated gene transfer. Decorin infection resulted in decreased protein levels of MMP-1 and MMP-3 whereas MMP-2 and TIMP-2 secretion was increased. MMP-9, MMP-13 and TIMP-1 were not affected by decorin infection. Cytokine measurements by ELISA showed that decorin overexpression reduced TGF-beta and IL-1beta. In contrast, IL-4 and TNF-alpha levels were markedly increased in decorin-infected cells. These results suggest that decorin could modulate the expression of certain metalloproteinases and their inhibitors, as well as the production of cytokines. Altogether, our data suggest that decorin might play a pivotal role in tissue remodeling by acting on the balance between extracellular matrix synthesis and degradation.
机译:Decorin是一种富含亮氨酸的小蛋白聚糖,在控制细胞增殖,细胞迁移,胶原原纤维形成和调节TGF-β的活性中发挥作用。在本研究中,我们调查了除芯蛋白对金属蛋白酶(MMP-1,-2,-3,-9和-13),金属蛋白酶组织抑制剂(TIMP-1,-2)和细胞因子(TGF)产生的影响-β,IL-1β,IL-4和TNF-α)。使用腺病毒介导的基因转移,Decorin在培养的人类牙龈成纤维细胞中过表达。 Decorin感染导致MMP-1和MMP-3蛋白质水平降低,而MMP-2和TIMP-2分泌增加。 MMP-9,MMP-13和TIMP-1不受甲壳素感染的影响。通过ELISA进行的细胞因子测量表明,核心蛋白聚糖过表达降低了TGF-beta和IL-1beta。相反,在被核心蛋白聚糖感染的细胞中,IL-4和TNF-α水平明显升高。这些结果表明,核心蛋白聚糖可以调节某些金属蛋白酶及其抑制剂的表达,以及细胞因子的产生。总而言之,我们的数据表明,核心蛋白聚糖可能通过作用于细胞外基质合成与降解之间的平衡而在组织重塑中发挥关键作用。

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