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cDNA microarray analysis of the differentially expressed genes involved in murine pre-osteoclast RAW264.7 cells proliferation stimulated by dexamethasone

机译:地塞米松刺激的小鼠破骨细胞RAW264.7细胞增殖中涉及的差异表达基因的cDNA微阵列分析

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摘要

Glucocorticoids (GCs) are hormones with anti-inflammatory and immuno-suppressive effects. The use of hormonal medicine like GCs may cause systemic adverse effects. In the present study, the cellular response of murine pre-osteoclast cell line RAW264.7 to dexamethasone (DEX) was investigated and the result demonstrated that DEX may stimulate RAW264.7 cells proliferation. Changes in gene expression involved in RAW264.7 cells proliferation stimulated by dexamethasone were investigated using cDNA microarrays containing 1000 cDNAs. It was found that 67 genes were regulated by DEX and could be grouped into 8 functional categories, including cell cycle regulation, cell survival, metabolism, pro-inflammatory effect, cytoskeleton, proteasome, signaling transduction and transcription factors. Moreover, some signaling pathways that involve in modulation of DEX on RAW264.7 cells functions were identified, including p53, 14-3-3 gamma, MAPK, Elk-1, I kappa B and Ifn related pathways. (c) 2007 Elsevier Inc. All rights reserved.
机译:糖皮质激素(GCs)是具有抗炎和免疫抑制作用的激素。使用激素类药物(如GC)可能会导致全身性不良反应。在本研究中,研究了鼠破骨细胞破细胞RAW264.7对地塞米松(DEX)的细胞应答,结果表明DEX可以刺激RAW264.7细胞增殖。使用包含1000个cDNA的cDNA微阵列研究了地塞米松刺激的RAW264.7细胞增殖所涉及的基因表达变化。发现有67个基因受DEX调控,可分为8个功能类别,包括细胞周期调控,细胞存活,代谢,促炎作用,细胞骨架,蛋白酶体,信号转导和转录因子。此外,鉴定了一些在RAW264.7细胞功能上涉及DEX调节的信号传导途径,包括p53、14-3-3γ,MAPK,Elk-1,IκB和Ifn相关途径。 (c)2007 Elsevier Inc.保留所有权利。

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