Department of Biochemistry, College of Life Science and Biotechnology, Yonsei University, Seoul 03722, Korea.
Graduate school of Pharmaceutical Sciences, College of Pharmacy, Ewha Womans University, Seoul 03790, Korea.
Int J Mol Sci. 2019 Jun 4;20(11):2734. doi: 10.3390/ijms20112734.
Skullcapflavone II is a flavonoid derived from the root of , a herbal medicine used for anti-inflammatory and anti-cancer therapies. We analyzed the effect of skullcapflavone II on the expression of matrix metalloproteinase-1 (MMP-1) and integrity of type I collagen in foreskin fibroblasts. Skullcapflavone II did not affect the secretion of type I collagen but reduced the secretion of MMP-1 in a dose- and time-dependent manner. Real-time reverse transcription-PCR and reporter gene assays showed that skullcapflavone II reduced MMP-1 expression at the transcriptional level. Skullcapflavone II inhibited the serum-induced activation of the extracellular signal-regulated kinase (ERK) and c-Jun N-terminal kinase (JNK) signaling pathways required for MMP-1 transactivation. Skullcapflavone II also reduced tumor necrosis factor (TNF)-α-induced nuclear factor kappa light chain enhancer of activated B cells (NF-κB) activation and subsequent MMP-1 expression. In three-dimensional culture of fibroblasts, skullcapflavone II down-regulated TNF-α-induced MMP-1 secretion and reduced breakdown of type I collagen. These results indicate that skullcapflavone II is a novel biomolecule that down-regulates MMP-1 expression in foreskin fibroblasts and therefore could be useful in therapies for maintaining the integrity of extracellular matrix.
黄芩素 II 是一种黄酮类化合物,来源于草药黄芩的根,用于抗炎和抗癌治疗。我们分析了黄芩素 II 对包皮成纤维细胞中基质金属蛋白酶-1(MMP-1)表达和 I 型胶原完整性的影响。黄芩素 II 不影响 I 型胶原的分泌,但以剂量和时间依赖的方式减少 MMP-1 的分泌。实时逆转录-PCR 和报告基因分析表明,黄芩素 II 可在转录水平降低 MMP-1 的表达。黄芩素 II 抑制了 MMP-1 反式激活所需的细胞外信号调节激酶(ERK)和 c-Jun N-末端激酶(JNK)信号通路的血清诱导激活。黄芩素 II 还减少了肿瘤坏死因子(TNF)-α诱导的核因子 kappa 轻链增强子的激活 B 细胞(NF-κB)激活和随后的 MMP-1 表达。在成纤维细胞的三维培养中,黄芩素 II 下调了 TNF-α诱导的 MMP-1 分泌,并减少了 I 型胶原的分解。这些结果表明,黄芩素 II 是一种新型生物分子,可下调包皮成纤维细胞中 MMP-1 的表达,因此可用于维持细胞外基质完整性的治疗。