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黄芩素 II 通过抑制人皮肤成纤维细胞中 MMP-1 的转录来抑制 I 型胶原的降解。

Skullcapflavone II Inhibits Degradation of Type I Collagen by Suppressing MMP-1 Transcription in Human Skin Fibroblasts.

机构信息

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.

出版信息

Int J Mol Sci. 2019 Jun 4;20(11):2734. doi: 10.3390/ijms20112734.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c685/6600147/59300694fc90/ijms-20-02734-g001.jpg

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