Wu Xingjing, Zhang Yongtao, Guo Xiong, Xu Hongguang, Xu Zhujun, Duan Dapeng, Wang Kunzheng
Department of Orthopedics, The Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi 710004, China.
Department of Orthopedics, The Affiliated Hospital of Qingdao University, Qingdao, Shandong 266061, China.
Gene. 2015 Jul 1;565(1):22-9. doi: 10.1016/j.gene.2015.03.072. Epub 2015 Apr 8.
Accumulating evidence has recently indicated a vital role of microRNAs (miRNAs) in the development of various bone diseases. However, the biological role of miRNAs in the pathogenesis of non-traumatic osteonecrosis of femoral head (ONFH) has not yet been investigated. The present study aimed to profile the differential miRNA expression between non-traumatic ONFH and femoral neck fracture and to develop further understanding of the molecular mechanisms involved in the pathogenesis of non-traumatic ONFH. Femoral heads from 4 patients with non-traumatic ONFH and 4 with femoral neck fracture were used to analyze the miRNA expression profiles in bone tissue using the Exiqon miRCURY™ LNA Array (v.18.0). The results of miRNA microarray analysis were further confirmed by real-time quantitative polymerase chain reaction (qPCR). The differentially expressed miRNA target genes and signaling pathways involved were predicted by bioinformatics analysis. MiRNA microarray chip analysis revealed that 22 miRNAs were significantly up-regulated and 17 were significantly down-regulated in the non-traumatic ONFH samples compared with the femoral neck fracture samples. The real-time qPCR also confirmed the microarray data. Bioinformatics analysis demonstrated that toll-like receptor (TLR), neurotrophin and NOD-like receptor signaling pathway were most likely to be regulated by these differential miRNAs. This miRNA microarray study reveals significant differences in miRNA expression between patients with non-traumatic ONFH and those with femoral neck fracture. Our data also manifests that the signaling pathways regulated by these differentially expressed miRNAs might be important in the pathogenesis of non-traumatic ONFH.
最近越来越多的证据表明,微小RNA(miRNA)在各种骨疾病的发展中起着至关重要的作用。然而,miRNA在非创伤性股骨头坏死(ONFH)发病机制中的生物学作用尚未得到研究。本研究旨在分析非创伤性ONFH与股骨颈骨折之间miRNA表达的差异,并进一步了解非创伤性ONFH发病机制中涉及的分子机制。使用Exiqon miRCURY™ LNA Array(v.18.0)对4例非创伤性ONFH患者和4例股骨颈骨折患者的股骨头进行分析,以检测骨组织中的miRNA表达谱。通过实时定量聚合酶链反应(qPCR)进一步证实了miRNA微阵列分析的结果。通过生物信息学分析预测了差异表达的miRNA靶基因和相关信号通路。miRNA微阵列芯片分析显示,与股骨颈骨折样本相比,非创伤性ONFH样本中有22种miRNA显著上调,17种显著下调。实时qPCR也证实了微阵列数据。生物信息学分析表明,Toll样受体(TLR)、神经营养因子和NOD样受体信号通路最有可能受这些差异miRNA的调控。这项miRNA微阵列研究揭示了非创伤性ONFH患者与股骨颈骨折患者之间miRNA表达的显著差异。我们的数据还表明,这些差异表达的miRNA调控的信号通路可能在非创伤性ONFH的发病机制中起重要作用。