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首页> 外文期刊>In vivo. >Expression of matrix metalloproteinases and their inhibitors by rat NK cells: inhibition of their expression by genistein.
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Expression of matrix metalloproteinases and their inhibitors by rat NK cells: inhibition of their expression by genistein.

机译:大鼠NK细胞表达基质金属蛋白酶及其抑制剂:染料木黄酮抑制其表达。

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摘要

In this study, we describe rat NK cell-derived MMPs including membrane-type MMPs (MT-MMPs) and tissue inhibitors of MMP (TIMPs). RT-PCR analysis from cDNA of rat A-NK cells revealed mRNA for MMP-2, MMP-9, MMP-7, MMP-10, MMP-11, MMP-13, MT1-MMP, MT2-MMP, TIMP-1, and TIMP-2. The RNK-16 cells expressed mRNA for MMP-7, MMP-10, MMP-11, MT1-MMP, MT2-MMP, TIMP-1, and TIMP-2, in addition to MMP-3 and MMP-13. Western blot analysis confirmed proteins for MT1-MMP and MT2-MMP in RNK-16 cells. TIMP-1 in rat A-NK cells was present at molecular mass of 34-kDa protein which may represent a highly glycosylated form. Genistein, a natural isoflavone found in soybeans, inhibited proliferation of RNK-16 cells in dosage dependent manner. In addition, it down-regulated the expression of MMP-13, MT1-MMP, TIMP-1 and TIMP-2. Moreover, genistein greatly impaired the ability of RNK-16 cells to invade through a model basement membrane. This effect might be mediated by the observed down-regulation of MMP-13 and MT1-MMP.
机译:在这项研究中,我们描述了大鼠NK细胞衍生的MMP,包括膜型MMP(MT-MMPs)和MMP的组织抑制剂(TIMPs)。大鼠A-NK细胞cDNA的RT-PCR分析显示MMP-2,MMP-9,MMP-7,MMP-10,MMP-11,MMP-13,MT1-MMP,MT2-MMP,TIMP-1的mRNA和TIMP-2。除了MMP-3和MMP-13,RNK-16细胞还表达MMP-7,MMP-10,MMP-11,MT1-MMP,MT2-MMP,TIMP-1和TIMP-2的mRNA。蛋白质印迹分析证实了RNK-16细胞中MT1-MMP和MT2-MMP的蛋白质。大鼠A-NK细胞中TIMP-1的分子质量为34-kDa,可能代表高度糖基化的形式。金雀异黄素是大豆中发现的天然异黄酮,它以剂量依赖的方式抑制RNK-16细胞的增殖。此外,它下调了MMP-13,MT1-MMP,TIMP-1和TIMP-2的表达。此外,金雀异黄素极大地损害了RNK-16细胞侵袭模型基底膜的能力。这种作用可能是由观察到的MMP-13和MT1-MMP的下调介导的。

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