Hu Jun, Liao Haojie, Ma Zebin, Chen Hongjiang, Huang Zhonglian, Zhang Yuantao, Yu Menglei, Chen Youbin, Xu Jiankun
Department of Orthopaedics, the First Affiliated Hospital, Shantou University Medical College, Guangdong Province, China.
The Sun-Yat-Sen Memorial Hospital, Sun-Yat-Sen University, Guangdong Province, China.
Sci Rep. 2016 Feb 11;6:20875. doi: 10.1038/srep20875.
Extracorporeal shockwave (ESW) has been shown of great potential in promoting the osteogenesis of bone marrow mesenchymal stem cells (BMSCs), but it is unknown whether this osteogenic promotion effect can also be achieved in other MSCs (i.e., tendon-derived stem cells (TDSCs) and adipose-derived stem cells (ADSCs)). In the current study, we aimed not only to compare the osteogenic effects of BMSCs induced by ESW to those of TDSCs and ADSCs; but also to investigate the underlying mechanisms. We show here that ESW (0.16 mj/mm(2)) significantly promoted the osteogenic differentiation in all the tested types of MSCs, accompanied with the downregulation of miR-138, but the activation of FAK, ERK1/2, and RUNX2. The enhancement of osteogenesis in these MSCs was consistently abolished when the cells were pretreated with one of the following conditions: overexpression of miR-138, FAK knockdown using specific siRNA, and U0126, implying that all of these elements are indispensable for mediating the effect of ESW. Moreover, our study provides converging genetic and molecular evidence that the miR-138-FAK-ERK1/2-RUNX2 machinery can be generally activated in ESW-preconditioned MSCs, suggesting that ESW may be a promising therapeutic strategy for the enhancement of osteogenesis of MSCs, regardless of their origins.
体外冲击波(ESW)已被证明在促进骨髓间充质干细胞(BMSC)成骨方面具有巨大潜力,但尚不清楚这种成骨促进作用是否也能在其他间充质干细胞(即肌腱衍生干细胞(TDSC)和脂肪衍生干细胞(ADSC))中实现。在本研究中,我们不仅旨在比较ESW诱导的BMSC与TDSC和ADSC的成骨效果,还旨在研究其潜在机制。我们在此表明,ESW(0.16 mj/mm(2))显著促进了所有测试类型间充质干细胞的成骨分化,同时伴有miR-138的下调,但FAK、ERK1/2和RUNX2的激活。当细胞用以下条件之一预处理时,这些间充质干细胞的成骨增强作用始终被消除:miR-138过表达、使用特异性siRNA敲低FAK以及U0126,这意味着所有这些因素对于介导ESW的作用都是不可或缺的。此外,我们的研究提供了一致的遗传和分子证据,表明miR-138-FAK-ERK1/2-RUNX2机制在ESW预处理的间充质干细胞中通常可以被激活,这表明ESW可能是一种有前途的治疗策略,用于增强间充质干细胞的成骨作用,无论其来源如何。