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首页> 外文期刊>Journal of Asian natural products research >Effects of osthole on apoptosis and TGF-besta_1 of hypertrophic scar fibroblasts
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Effects of osthole on apoptosis and TGF-besta_1 of hypertrophic scar fibroblasts

机译:蛇床子素对肥厚性瘢痕成纤维细胞凋亡和TGF-besta_1的影响

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摘要

Osthole, 7-methoxy-8-[3-methylpent-2-enyl]coumarin (1), was extracted from a Chinese herb Cnidium monnieri (L.) Cuss. It showed immunity strengthening, anti-tumor, anti-hepatitis, and anti-osteoporosis activities in previous studies. Our goals are to study the effects of 1 on cell proliferation and TGF-beta of hypertrophic scar fibroblasts. Our results showed that 1 induced apoptosis and inhibited cell proliferation in hypertrophic scar fibroblasts. 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay showed that its IC_(50) value toward hypertrophic scar fibroblasts was 15.5 +- 2.2 mumol/l. Furthermore, the results of cell growth curve matched with the above results. Inducing apoptosis by 1 in hypertrophic scar fibroblasts was assessed by various morphological and biochemical characteristics, including cell shrinkage, chromatin condensation, membrane blebbing, formation of apoptotic bodies, and DNA ladder formation. A typical 'Sub-G_1 peak' was also checked through flow cytometry. We used immunohistochemistry to observe the expression of TGF-beta_1. Also, we found that 1 could obviously inhibit the expression of TGF-beta_1 of fibroblasts derived from hypertrophic scar compared with the control group (P < 0.05). These results suggest that 1 inhibits the growth of hypertrophic scar fibroblasts through apoptosis and decreases the expression of TGF-beta_1
机译:从中草药Cnidium monnieri(L.)Cuss中提取出7-甲氧基-8- [3-甲基戊-2-烯基]香豆素(1)的臭虫。在以前的研究中,它显示出增强免疫力,抗肿瘤,抗肝炎和抗骨质疏松的活性。我们的目标是研究1对肥厚性瘢痕成纤维细胞的细胞增殖和TGF-β的影响。我们的结果表明1在肥厚性瘢痕成纤维细胞中诱导凋亡并抑制细胞增殖。 3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四唑溴化物(MTT)分析表明,其对肥厚性瘢痕成纤维细胞的IC_(50)值为15.5±2.2μmol/ l。此外,细胞生长曲线的结果与上述结果一致。通过各种形态学和生化特征,包括细胞收缩,染色质浓缩,膜起泡,凋亡小体形成和DNA梯形形成,对肥厚性瘢痕成纤维细胞中1诱导的凋亡进行了评估。还通过流式细胞仪检查了典型的“ Sub-G_1峰”。我们使用免疫组织化学观察了TGF-beta_1的表达。此外,我们发现,与对照组相比,1可以明显抑制肥厚性瘢痕来源的成纤维细胞TGF-β_1的表达(P <0.05)。这些结果表明1通过凋亡抑制增生性瘢痕成纤维细胞的生长,并降低TGF-beta_1的表达。

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