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丹酚酸B通过激活ERK信号通路促进人间充质干细胞的成骨分化。

Salvianolic acid B promotes osteogenesis of human mesenchymal stem cells through activating ERK signaling pathway.

作者信息

Xu Daohua, Xu Liangliang, Zhou Chenhui, Lee Wayne Y W, Wu Tie, Cui Liao, Li Gang

机构信息

Department of Pharmacology, Guangdong Medical College, Dongguan, PR China; Department of Orthopaedics & Traumatology, The Chinese University of Hong Kong, Prince of Wales Hospital, Shatin, Hong Kong, China.

Department of Orthopaedics & Traumatology, The Chinese University of Hong Kong, Prince of Wales Hospital, Shatin, Hong Kong, China; Li Ka Shing Institute of Health Sciences, The Chinese University of Hong Kong, Prince of Wales Hospital, Shatin, Hong Kong, China; Lui Che Woo Institute of Innovative Medicine, Faculty of Medicine, The Chinese University of Hong Kong, Hong Kong, China.

出版信息

Int J Biochem Cell Biol. 2014 Jun;51:1-9. doi: 10.1016/j.biocel.2014.03.005. Epub 2014 Mar 19.

Abstract

Salvianolic acid B, a major bioactive component of Chinese medicine herb, Salvia miltiorrhiza, is widely used for treatment of cardiovascular diseases. Our recent studies have shown that Salvianolic acid B can prevent development of osteoporosis. However, the underlying mechanisms are still not clarified clearly. In the present study, we aim to investigate the effects of Salvianolic acid B on viability and osteogenic differentiation of human mesenchymal stem cells (hMSCs). The results showed Salvianolic acid B (Sal B) had no obvious toxic effects on hMSCs, whereas Sal B supplementation (5μM) increased the alkaline phosphatase activity, osteopontin, Runx2 and osterix expression in hMSCs. Under osteogenic induction condition, Sal B (5μM) significantly promoted mineralization; and when the extracellular-signal-regulated kinases signaling (ERK) pathway was blocked, the anabolic effects of Sal B were diminished, indicating that Sal B promoted osteogenesis of hMSCs through activating ERK signaling pathway. The current study confirms that Sal B promotes osteogenesis of hMSCs with no cytotoxicity, and it may be used as a potential therapeutic agent for the management of osteoporosis.

摘要

丹酚酸B是中药丹参的主要生物活性成分,广泛用于治疗心血管疾病。我们最近的研究表明,丹酚酸B可以预防骨质疏松症的发展。然而,其潜在机制仍未完全阐明。在本研究中,我们旨在研究丹酚酸B对人骨髓间充质干细胞(hMSCs)活力和成骨分化的影响。结果表明,丹酚酸B(Sal B)对hMSCs没有明显的毒性作用,而补充Sal B(5μM)可增加hMSCs中的碱性磷酸酶活性、骨桥蛋白、Runx2和osterix表达。在成骨诱导条件下,Sal B(5μM)显著促进矿化;当细胞外信号调节激酶信号(ERK)通路被阻断时,Sal B的合成代谢作用减弱,表明Sal B通过激活ERK信号通路促进hMSCs的成骨作用。目前的研究证实,Sal B可促进hMSCs的成骨作用且无细胞毒性,它可能作为一种潜在的治疗药物用于骨质疏松症的治疗。

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