Zhang Wei, Zhang LiCheng, Zhou Yan, Ji XinRan, Liu JianHeng, Liu DaoHong, Yin Peng, Peng Ye, Hao Ming, Zhang LiHai, Tang PeiFu
Department of Orthopaedics, General Hospital of Chinese PLA, No. 28 Fuxing Road, Haidian District, Beijing 100853, China.
Medical Department, Affiliated Hospital of Chinese PLA General Hospital, Beijing 100048, China.
Biomed Res Int. 2015;2015:309747. doi: 10.1155/2015/309747. Epub 2015 Nov 1.
Various stimulators have been reported to promote MSC osteogenic differentiation via different pathways such as bone morphogenetic protein 9 (BMP9) through influencing COX-2 and miR-548d-5p through targeting peroxisome proliferator-activated receptor-γ (PPARγ). Whether synergistic effects between BMP9 and miR-548d-5p existed in promoting osteogenesis from MSCs was unclear. In the study, the potential synergistic effects of BMP9 and miR-548d-5p on human MSC differentiation were investigated. Osteogenic differentiation of MSCs treated with BMP9 or miR-548d-5p was detected with multimodality of methods. The results demonstrated that BMP9 and miR-548d-5p significantly influenced COX-2 and PPARγ, respectively. BMP9 also influenced the expression of PPARγ, but no significant effect of miR-548d-5p on COX-2 was observed. When BMP9 and miR-548d-5p were combined, more potent effects on both COX-2 and PPARγ were observed than BMP9 or miR-548d-5p alone. Consistently, osteogenic analysis at different timepoints demonstrated that osteogenic genes, ALP activity, calcium deposition, OPN protein, and matrix mineralization were remarkably upregulated by BMP9/miR-548d-5p compared with BMP9 or miR-548d-5p alone, indicating the synergetic effects of BMP9 and miR-548d-5p on osteogenic differentiation of MSCs. Our study demonstrated that regulating different osteogenic regulators may be an effective strategy to promote bone tissue regeneration for bone defects.
据报道,各种刺激物可通过不同途径促进间充质干细胞(MSC)的成骨分化,例如骨形态发生蛋白9(BMP9)通过影响环氧化酶-2(COX-2)以及通过靶向过氧化物酶体增殖物激活受体γ(PPARγ)影响微小RNA-548d-5p(miR-548d-5p)。目前尚不清楚BMP9与miR-548d-5p在促进MSC成骨过程中是否存在协同作用。在本研究中,我们对BMP9与miR-548d-5p在人MSC分化方面的潜在协同作用进行了研究。采用多种方法检测了经BMP9或miR-548d-5p处理的MSC的成骨分化情况。结果表明,BMP9和miR-548d-5p分别对COX-2和PPARγ有显著影响。BMP9也影响PPARγ的表达,但未观察到miR-548d-5p对COX-2有显著影响。当BMP9与miR-548d-5p联合使用时,与单独使用BMP9或miR-548d-5p相比,对COX-2和PPARγ均观察到更强的作用。同样,在不同时间点进行的成骨分析表明,与单独使用BMP9或miR-548d-5p相比,BMP9/miR-548d-5p显著上调了成骨基因水平、碱性磷酸酶(ALP)活性、钙沉积、骨桥蛋白(OPN)蛋白水平以及基质矿化水平,表明BMP9与miR-548d-5p对MSC的成骨分化具有协同作用。我们的研究表明,调节不同的成骨调节因子可能是促进骨缺损骨组织再生的有效策略。