State Key Laboratory of Oral Diseases, Sichuan University, Prosthodontics Department, West China Stomatology Hospital, Chengdu, People's Republic of China.
Cell Biol Int. 2010 Mar 19;34(5):425-32. doi: 10.1042/CBI20090061.
Although osteocytes have long been regarded as mechanosensors for translating mechanical signals into biochemical signals to regulate the other bone cells, the global gene expression patterns and pathways of osteocytes responding to mechanical stimulation are not well defined. We investigated CCF (cyclic compressive force) responsive gene expression patterns at different time-points using Mouse genome-wide oligonucleotide microarrays with an osteocyte-like MLO-Y4 cell model. We performed a SOM (self-organizing maps) clustering algorithm based on pattern similarity to organize clusters of temporal expression patterns, and used qRT-PCR (quantitative reverse transcriptase PCR) analysis to validate expression patterns of selected genes. We also used functional and pathway analysis to evaluate the biological features of the data. In this study, we derived a biological hypothesis from the gene expression profiles that CCF triggers a tightly regulated transcriptional programme to induce bone resorption cell signalling and involves common pathways in osteocytes.
尽管破骨细胞长期以来一直被认为是将机械信号转化为生化信号的机械传感器,以调节其他骨细胞,但破骨细胞对机械刺激的整体基因表达模式和途径尚未得到很好的定义。我们使用类似于成骨细胞的 MLO-Y4 细胞模型的 Mouse genome-wide oligonucleotide microarrays,研究了 CCF(循环压缩力)对不同时间点基因表达模式的响应。我们使用基于模式相似性的 SOM(自组织映射)聚类算法对时间表达模式进行聚类组织,并使用 qRT-PCR(定量逆转录聚合酶链反应)分析来验证所选基因的表达模式。我们还使用功能和途径分析来评估数据的生物学特征。在这项研究中,我们从基因表达谱中得出了一个生物学假设,即 CCF 触发了一个严格调控的转录程序,以诱导骨吸收细胞信号,并涉及破骨细胞中的常见途径。