Z Zhu, T Tang, Z He, F Wang, H Chen, G Chen, J Zhou, S Liu, J Wang, W Tian, D Chen, X Wu, X Liu, Z Zhou, S Liu
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The expression of runt-related transcription factor 2, collagen I, osterix, osteocalcin and alkaline phosphatase were compared between the static and the experimental groups. In addition, the cytoskeleton was detected using phalloidin staining while YAP phosphorylation states and nuclear location were identified using immunofluorescence. The results showed that mechanical stretching loading increased the expression of osteogenic genes and proteins in the OPLL group, while it had no significant effect on the control group. When OPLL cells were stretched, YAP exhibited an obvious nuclear translocation and the Wnt/β-catenin pathway was activated. Knocking down YAP or β-catenin could weaken the impact upon osteogenic differentiation induced by mechanical stimulation. 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引用次数: 1
摘要
后纵韧带骨化(OPLL)的发病机制尚不清楚。机械刺激是OPLL的重要致病因素之一。yes-associated protein (YAP)作为机械刺激转导信号之一,与Wnt/β-catenin信号通路相互作用,在成骨分化中发挥重要作用。本研究旨在证明YAP-Wnt/β-catenin轴在机械应力诱导的细胞分化中的作用。取OPLL和非OPLL患者后纵韧带组织原代细胞进行单轴正弦循环拉伸(5%,0.5 Hz, 3 d),比较静态组和实验组中矮型相关转录因子2、ⅰ型胶原、骨蛋白、骨钙素和碱性磷酸酶的表达。此外,使用phalloidin染色检测细胞骨架,使用免疫荧光鉴定YAP磷酸化状态和核位置。结果显示,机械拉伸载荷增加了OPLL组成骨基因和成骨蛋白的表达,而对对照组无显著影响。当OPLL细胞被拉伸时,YAP表现出明显的核易位,Wnt/β-catenin通路被激活。抑制YAP或β-catenin可减弱机械刺激对成骨分化的影响。yap介导的机械刺激通过Wnt/β-catenin通路促进OPLL细胞成骨分化,且该过程不依赖于Hippo通路。
Uniaxial cyclic stretch enhances osteogenic differentiation of OPLL-derived primary cells via YAP-Wnt/β-catenin axis.
The pathogenesis of posterior longitudinal ligament ossification (OPLL) remains inadequately understood. Mechanical stimulation is one of the important pathogenic factors in OPLL. As one of the mechanical stimulation transduction signals, the yes-associated protein (YAP) interacts with the Wnt/β-catenin signalling pathway, which plays an important role in osteogenic differentiation. This study aimed to demonstrate the role of YAP-Wnt/β-catenin axis in cell differentiation induced by mechanical stress. Primary cells extracted from posterior longitudinal ligament tissues from OPLL or non-OPLL patients were subjected to sinusoidal uniaxial cyclic stretch (5 %, 0.5 Hz, 3 d). The expression of runt-related transcription factor 2, collagen I, osterix, osteocalcin and alkaline phosphatase were compared between the static and the experimental groups. In addition, the cytoskeleton was detected using phalloidin staining while YAP phosphorylation states and nuclear location were identified using immunofluorescence. The results showed that mechanical stretching loading increased the expression of osteogenic genes and proteins in the OPLL group, while it had no significant effect on the control group. When OPLL cells were stretched, YAP exhibited an obvious nuclear translocation and the Wnt/β-catenin pathway was activated. Knocking down YAP or β-catenin could weaken the impact upon osteogenic differentiation induced by mechanical stimulation. YAP-mediated mechanical stimulation promoted osteogenic differentiation of OPLL cells through Wnt/β-catenin pathway and this progress was independent of the Hippo pathway.
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