Li Chen-Shuang, Zheng Zhong, Su Xiao-Xia, Wang Fei, Ling Michelle, Zou Min, Zhou Hong
Key Laboratory of Shaanxi Province for Craniofacial Precision Medicine Research, College of Stomatology, Xi'an Jiaotong University, Xi'an, Shaanxi 710004, China; Department of Orthodontics, College of Stomatology, Xi'an Jiaotong University, Xi'an, Shaanxi 710004, China.
Division of Growth and Development and Section of Orthodontics, School of Dentistry, University of California, Los Angeles, CA 90095, USA.
Biomed Res Int. 2016;2016:3764372. doi: 10.1155/2016/3764372. Epub 2016 Feb 16.
Human umbilical cord mesenchymal stem cells (hUCMSCs) are recognized as candidate progenitor cells for bone regeneration. However, the mechanism of hUCMSC osteogenesis remains unclear. In this study, we revealed that mitogen-activated protein kinases (MAPKs) signaling is involved in hUCMSC osteogenic differentiation in vitro. Particularly, the activation of c-Jun N-terminal kinases (JNK) and p38 signaling pathways maintained a consistent level in hUCMSCs through the entire 21-day osteogenic differentiation period. At the same time, the activation of extracellular signal-regulated kinases (ERK) signaling significantly increased from day 5, peaked at day 9, and declined thereafter. Moreover, gene profiling of osteogenic markers, alkaline phosphatase (ALP) activity measurement, and alizarin red staining demonstrated that the application of U0126, a specific inhibitor for ERK activation, completely prohibited hUCMSC osteogenic differentiation. However, when U0126 was removed from the culture at day 9, ERK activation and osteogenic differentiation of hUCMSCs were partially recovered. Together, these findings demonstrate that the activation of ERK signaling is essential for hUCMSC osteogenic differentiation, which points out the significance of ERK signaling pathway to regulate the osteogenic differentiation of hUCMSCs as an alternative cell source for bone tissue engineering.
人脐带间充质干细胞(hUCMSCs)被认为是骨再生的候选祖细胞。然而,hUCMSC成骨的机制仍不清楚。在本研究中,我们揭示丝裂原活化蛋白激酶(MAPKs)信号通路参与体外hUCMSC的成骨分化。特别是,在整个21天的成骨分化期,c-Jun氨基末端激酶(JNK)和p38信号通路的激活在hUCMSCs中维持在一致水平。同时,细胞外信号调节激酶(ERK)信号通路的激活从第5天开始显著增加,在第9天达到峰值,此后下降。此外,成骨标志物的基因谱分析、碱性磷酸酶(ALP)活性测定和茜素红染色表明,ERK激活的特异性抑制剂U0126的应用完全抑制了hUCMSC的成骨分化。然而,当在第9天从培养物中去除U0126时,hUCMSCs的ERK激活和成骨分化部分恢复。总之,这些发现表明ERK信号通路的激活对hUCMSC的成骨分化至关重要,这指出了ERK信号通路在调节hUCMSCs成骨分化作为骨组织工程替代细胞来源方面的重要性。