Longhua Hospital and Key Laboratory of Ministry of Education of China, Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Department of Orthopedic Surgery, LSU Health Sciences Center, Shreveport, LA, USA.
Sci Rep. 2017 Aug 1;7(1):7002. doi: 10.1038/s41598-017-07633-7.
Oleanolic acid (OA), a pentacyclic triterpenoid, has been shown to modulate multiple signaling pathways in a variety of cell linages. But the mechanisms underlying OA-mediated mesenchymal stromal cell (MSC) osteogenic differentiation are not known. In this study, we examined effects of OA on cell viability, osteogenic differentiation in MSCs, and the involvement of Notch and BMP signaling. OA induced bone marrow derived MSC differentiation towards osteoprogenitor cells and inhibited Notch signaling in a dose dependent manner. Constitutive activation of Notch signaling fully blocked OA induced MSC osteogenic differentiation. The expression level of early osteogenic marker genes, ALP, Runx2, and type I collagen, which play a critical role in MSC to osteoblast transition and servers as a downstream target of BMP signaling, was significantly induced by OA. Furthermore, BMP2 mediated MSC osteogenic differentiation was significantly enhance by OA treatment, indicating a synergistic effect between BMP2 and OA. Our results suggest that OA is a promising bioactive agent for bone tissue regeneration, and inhibition of Notch signaling is required for its osteogenic effects on MSCs.
齐墩果酸(OA)是一种五环三萜,已被证明可调节多种细胞谱系中的多种信号通路。但是,OA 介导间充质基质细胞(MSC)成骨分化的机制尚不清楚。在这项研究中,我们研究了 OA 对细胞活力,MSC 成骨分化的影响以及 Notch 和 BMP 信号的参与。OA 诱导骨髓来源的 MSC 向成骨前体细胞分化,并呈剂量依赖性抑制 Notch 信号。Notch 信号的组成性激活完全阻止了 OA 诱导的 MSC 成骨分化。ALP、Runx2 和 I 型胶原等早期成骨标记基因的表达水平显着受 OA 诱导,这些基因在 MSC 向成骨细胞的转化中起关键作用,并且是 BMP 信号的下游靶标。此外,OA 处理显着增强了 BMP2 介导的 MSC 成骨分化,表明 BMP2 和 OA 之间存在协同作用。我们的研究结果表明,OA 是一种有前途的骨组织再生生物活性物质,并且抑制 Notch 信号对于 OA 对 MSC 的成骨作用是必需的。