TGF- β 1介导全反式维甲酸上调大鼠系膜细胞中MMP-2的表达

W. Lin , N. Zhang , S. Zhang , J. Gu , M. Guo
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引用次数: 0

摘要

基质金属蛋白酶-2(MMP-2)降解基底膜胶原,其异常表达与肾小球肾炎和肾小球硬化有关。全反式维甲酸(ATRA)已被证明可以预防年龄相关性肾小球硬化。我们的研究结果表明,ATRA上调了培养的系膜细胞中MMP-2mRNA的表达和MMP-2蛋白的分泌,并增加了MMP-2的酶活性。此外,ATRA还引起转化生长因子-β(TGF-β1)肽分泌的剂量依赖性增加。由于TGF-β1调节系膜细胞中MMP-2的表达,因此TGF-β1可能参与ATRA诱导的MMP-2表达。使用反义TGF-β1 RNA策略,反义TGF-β1构建体几乎完全阻断了反义转染子中活性TGF-β1-肽的分泌。Northern印迹分析显示,用10–6M ATRA处理72小时的转染子既不增加也不降低MMP-2信使核糖核酸(mRNA)的水平。此外,在存在10–6M ATRA的情况下,向系膜细胞添加抗TGF-β1抗体可剂量依赖性地降低ATRA诱导的MMP-2表达。这些数据表明TGF-β1可能参与ATRA诱导的MMP-2表达。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Upregulation of MMP-2 by all-trans retinoic acid is mediated by TGF- β 1 in cultured rat mesangial cell

Matrix metalloproteinase-2 (MMP-2) degrades basement membrane collagen and its abnormal expression is associated with glomerulonephritis and glomerulosclerosis. All-trans retinoic acid (ATRA) has been indicated as preventing age-related glomerulosclerosis. The results of our study showed that ATRA upregulated expression of MMP-2 mRNA and secretion of MMP-2 proteins, and increased enzymatic activity of MMP-2 in cultured mesangial cell. In addition, ATRA also caused a dose-dependent increase in the secretion of transforming growth factor-β (TGF-β1) peptides. Since TGF-β1 regulated the expression of MMP-2 in mesangial cell, it is possible that TGF-β1 is involved in ATRA-induced MMP-2 expression. Using antisense TGF-β1 RNA strategy, antisense TGF-β1 construct almost completely blocked secretion of active TGF-β1 peptides in the antisense-bearing transfectants. Northern blot analysis showed that the transfectants treated with 10–6M ATRA for 72 h neither increased nor decreased the levels of MMP-2 messenger ribonucleic acid (mRNA). Moreover, addition of anti-TGF-β1 antibodies to mesangial cell in the presence of 10–6M ATRA reduced ATRA-induced MMP-2 expression dose dependently. These data suggest that TGF-β1 might be involved in ATRA-induced MMP-2 expression.

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