机械牵张应力刺激成骨细胞的差异蛋白质组学研究
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国家自然科学基金资助项目 (30870594)


Differential proteomic analysis on osteoblasts stimulated by mechanical strain
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    摘要:

    目的 应用蛋白质组学方法分析人成骨样细胞Saos2在牵张应力作用下蛋白质表达的差异,为更全面地阐明成骨细胞对牵张应力的反应机制提供分子基础。方法 将Saos2分为加力组与对照组,采用Flexcell牵张应力加载系统,用12%大小的应力值进行力学刺激24 h后,应用蛋白质双向凝胶电泳分离蛋白样品,质谱技术鉴定差异表达蛋白点,并用生物信息学分析差异蛋白参与的生物学过程和主要功能。结果 对照组和加力组分别得到 (1031±41)和 (928±25)个蛋白质点,质谱鉴定出肽酰脯氨酰异构酶A样3、线粒体ATP合成酶、抗氧化蛋白1、丝切蛋白1、蛋白磷酸酶1、延伸因子2等17个表达增高的差异蛋白质,涉及应激反应、能量代谢、细胞增殖、细胞骨架重建、信号转导及成骨分化等生物学功能。结论 成骨细胞在机械牵张应力作用下蛋白表达发生显著变化,这些差异蛋白参与了成骨细胞力学反应机制的不同过程。

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    Objective To identify the differentially expressed proteins and clarify the major proteins involved in the molecular mechanism of osteoblasts under mechanical strain loading. Method Saos2 osteoblastic cells were subjected to 12% elongation for 24 hours by using Flexcell strain loading system. Proteins extracted from Saos2 cells were separated by twodimensional electrophoresis (2DE). Differential expressed protein spots among groups were submitted to matrixassisted laser desorption/ionization time of flight mass spectrometer (MALDITOF MS) assay and peptide mass fingerprinting (PMF) identification. The SwissProt and NCBI databases were used to obtain further information about proteins identified. Results Saos2 stimulated by mechanical strain showed a significant difference in 2DE system compared with the control group. A total of (1031±41) or (928±25) protein spots were resolved by 2DE of controls or experimental groups extractions respectively. 17 significant up  regulated proteins were identified. These associated proteins fell into 6 groups, including stress reaction, energy metabolism, cell proliferation, reconstruction of cytoskeleton, signaling and osteogenesis. Conclusions The Saos2 can express differential proteins stimulated by mechanical strains and these proteins may play an important role in molecular mechanism of osteoblasts under mechanical strain loading.

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李菲菲,丁寅,冯雪,王欢,陈富林,李立文.机械牵张应力刺激成骨细胞的差异蛋白质组学研究[J].医用生物力学,2010,25(6):406-411

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  • 收稿日期:2010-11-16
  • 最后修改日期:2010-11-22
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