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阿魏酸内酯通过靶向 Sonic Hedgehog 通路促进间充质干细胞的软骨分化。

Targeting of the Sonic Hedgehog pathway by atractylenolides promotes chondrogenic differentiation of mesenchymal stem cells.

机构信息

School of Chinese Herbal Medicine, Guangzhou University of Chinese Medicine, Guangzhou, China.

出版信息

Biol Pharm Bull. 2012;35(8):1328-35. doi: 10.1248/bpb.b12-00265.

Abstract

Molecules that enhance chondrogenic differentiation in mesenchymal stem cells (MSCs) were identified and isolated using an in vitro Gli reporter gene assay in MSCs incorporating a Sonic Hedgehog (Shh) target. Atractylenolide III, which promoted Gli1-mediated transcriptional activity, was isolated from an ethyl acetate extract of the Rhizoma, Atractylodis macrocephalae. After dehydration, atractylenolide III was transformed to atractylenolide I. Both atractylenolides were confirmed by MS, UV, IR, 1H- and 13C-NMR spectra. Atractylenolide III (which contains -OH at the 8-position) and atractylenolide I (which lacks -OH at the 8-position) were found to effectively promote the activity of the Gli promoter. While the hydroxyl group of atractylenolide III was not essential for the effect of atractylenolide, its effect was dependent on Shh signaling. Phenotypic cellular analysis indicated that atractylenolides induced MSCs to differentiate into chondrocytes, as shown by increased expression of specific chondrogenic markers including collagen II, aggrecan and the cartilage related transcription factor, Sox9. Atractylenolides significantly increased the expression of Shh and its target gene Gli-1, indicating that Shh signaling was activated by atractylenolides. Moreover, inhibition of Shh signaling reduced the effect of atractylenolides on the chondrogenic phenotype. The discovery that atractylenolides induce chondrocytes from MSCs is promising for bony disease therapy.

摘要

从整合了 Sonic Hedgehog(Shh)靶标的间充质干细胞(MSCs)的体外 Gli 报告基因测定中鉴定和分离了增强 MSCs 软骨分化的分子。从白术根茎的乙酸乙酯提取物中分离出了促进 Gli1 介导的转录活性的苍术内酯 III。苍术内酯 III 经脱水后转化为苍术内酯 I。通过 MS、UV、IR、1H-和 13C-NMR 谱证实了这两种苍术内酯的存在。苍术内酯 III(8 位含有-OH)和苍术内酯 I(8 位不含-OH)均能有效促进 Gli 启动子的活性。虽然苍术内酯 III 的羟基对苍术内酯的作用不是必需的,但它的作用取决于 Shh 信号。表型细胞分析表明,苍术内酯诱导 MSCs 分化为软骨细胞,具体表现在特异性软骨标志物如胶原 II、聚集蛋白聚糖和软骨相关转录因子 Sox9 的表达增加。苍术内酯显著增加了 Shh 及其靶基因 Gli-1 的表达,表明 Shh 信号被苍术内酯激活。此外,Shh 信号的抑制降低了苍术内酯对软骨表型的作用。苍术内酯诱导 MSCs 产生软骨细胞的发现为骨疾病治疗提供了希望。

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