PO-046 Gene expression profiling of peripheral blood mononuclear cells in young male trampoline athletes

Li Gao, Yongjie Yang, Enyuan Li, J. Mao
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Abstract

Objective Evidence indicates that physical activity influence bone health. However, the molecular mechanisms mediating the beneficial adaptations to exercise are not well understood. The purpose of this study was to examine the differentially expressed genes in PBMC between athletes and healthy controls, and to analyze the important functional genes and signal pathways that cause increased bone mineral density in athletes, in order to further reveal the molecular mechanisms of exercise promoting bone health. Methods Five professional trampoline athletes and five age-matched untrained college students participated in this study. Used the human expression Microarray V4.0 expression profiling chip to detect differentially expressed genes in the two groups, and performed KEGG Pathway analysis and application of STRING database to construct protein interaction Network; Real-Time PCR technology was used to verify the expression of some differential genes.  Results Compared with healthy controls, there were significant improvement in lumbar spine bone mineral density, and 236 up-regulated as well as 265 down-regulated in serum samples of athletes. The differentially expressed genes involved 28 signal pathways, such as cell adhesion molecules. Protein interaction network showed that MYC was at the core node position. Real-time PCR results showed that the expression levels of CD40 and ITGα6 genes in the athletes were up-regulated compared with the healthy controls, the detection results were consistent with that of the gene chip. Conclusions The findings highlight that long-term high-intensity trampoline training could induce transcriptional changes in PBMC of the athletes. These data suggest that gene expression fingerprints can serve as a powerful research tool to design novel strategies for monitoring exercise. The findings of the study also provide support for the notion that PBMC could be used as a substitute to study exercise training that affects bone health.
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年轻男性蹦床运动员外周血单核细胞PO-046基因表达谱分析
客观证据表明,体育活动影响骨骼健康。然而,介导对运动的有益适应的分子机制尚不清楚。本研究旨在检测运动员与健康对照者PBMC中差异表达基因,分析导致运动员骨密度增高的重要功能基因和信号通路,进一步揭示运动促进骨骼健康的分子机制。方法以5名专业蹦床运动员和5名年龄匹配的大学生为研究对象。使用human expression Microarray V4.0表达谱芯片检测两组差异表达基因,并进行KEGG Pathway分析,应用STRING数据库构建蛋白互作网络;采用Real-Time PCR技术验证部分差异基因的表达情况。结果与健康对照相比,运动员腰椎骨密度有明显改善,血清中有236个骨密度上调,265个骨密度下调。差异表达基因涉及28个信号通路,如细胞粘附分子。蛋白相互作用网络显示MYC位于核心节点位置。Real-time PCR结果显示,运动员体内CD40和ITGα6基因表达水平较健康对照上调,检测结果与基因芯片检测结果一致。结论长期高强度蹦床训练可引起运动员PBMC的转录改变。这些数据表明,基因表达指纹图谱可以作为一种强大的研究工具,用于设计监测运动的新策略。这项研究的发现也为PBMC可以作为研究运动训练影响骨骼健康的替代品的观点提供了支持。
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