动态流体剪切作用下T/C-28a2软骨细胞微阵列分析

J. Abulencia, R. Gaspard, John Quackenbush, K. Konstantopoulos
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引用次数: 0

摘要

使用32,448个元件的微阵列检测了软骨细胞系T/C-28a2在剪切流下的行为。平行板流室产生20 dyn/cm/sup 2/的剪切应力水平,持续1.5或24小时(h),之后测量基因调控。微阵列分析显示,在两个时间点,影响增殖/分化、细胞外基质/细胞骨架和炎症的基因受到差异调节。核糖核酸酶保护试验对基因子集进行,以确认从微阵列获得的数据。然而,对类风湿性关节炎(RA)患者炎症组织和滑膜中前列腺素生成的环氧化酶-2 (COX-2)基因进行了进一步的研究。Western杂交显示COX-2蛋白在24 h时存在,但在6或12 h时不存在。免疫荧光显微镜显示COX-2蛋白在剪切24 h后定位于细胞质中,在1.5 h后不存在。通过检测不同动态流体剪切条件下软骨细胞的整体基因表达谱,可能对类风湿性关节炎等软骨相关疾病的发病机制产生新的见解。
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Microarray analysis of the chondrocytic cell line T/C-28a2 under dynamic fluid shear
The behavior of the chondrocytic cell line T/C-28a2 under shear flow was examined using a 32,448 element microarray. A parallel plate flow chamber was used to generate a shear stress level of 20 dyn/cm/sup 2/ for 1.5 or 24 hours (h), after which gene regulation was measured. Microarray analysis revealed differentially regulated genes affecting proliferation/differentiation, extracellular matrix/cytoskeleton, and inflammation at both time points. A ribonuclease protection assay was performed on a subset of genes to confirm the data obtained from the microarray. However, the cyclooxygenase-2 (COX-2) gene, which plays a role in the prostaglandin production in inflamed tissues and the synovium of rheumatoid arthritis (RA) patients, was studied further. Western hybridization revealed that COX-2 protein is present at 24 h, but not at 6 or 12 h. Also, immunofluorescence microscopy shows that COX-2 protein localizes in the cytosol after 24 h of shear, and is not present after 1.5 h. By examining the overall gene expression profiles of chondrocytes under different conditions of dynamic fluid shear, new insights on the pathogenesis of cartilage related diseases such as rheumatoid arthritis might be generated.
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