›› 2016, Vol. 36 ›› Issue (2): 101-104.

• 基础研究 • 上一篇    下一篇

低氧诱导因子-2α在不同应力加载髁突软骨细胞中的表达及意义

李文1,丁王辉1,谈龙2,施洁珺1   

  1. 1. 浙江大学医学院附属口腔医院
    2. 浙江大学附属口腔医学院
  • 收稿日期:2015-08-28 修回日期:2015-11-08 出版日期:2016-02-28 发布日期:2016-02-29
  • 通讯作者: 施洁珺 E-mail:sjiejun2013@163.com
  • 基金资助:
    浙江省自然科学基金项目;浙江省科技厅公益技术应用研究项目

The expression and significance of HIF2α in condyle chondrocytes under different stress loadings

  • Received:2015-08-28 Revised:2015-11-08 Online:2016-02-28 Published:2016-02-29

摘要: [摘要] 目的 研究低氧诱导因子-2α(HIF-2α)及其下游分解代谢因子(MMP3,MMP13,ADAMTs-4)在不同应力加载髁突软骨细胞中的表达变化情况。方法 对培养到第3代的新生SD大鼠髁突软骨细胞采用5%的低氧培养箱培养。0.5 Hz下分别加载0,1 000,2 000,4 000单位压力,2 h后立即收集样本,台盼蓝染色,光镜下观察细胞形态并计数细胞数,计算死细胞率。采用westernblot及RTPCR技术检测HIF-2α及其下游分解代谢因子(MMP3, MMP13,ADAMTs-4)的蛋白及基因表达。结果 随着压力的增加,髁突软骨细胞死亡率显著上升(P<0.05)。HIF-2α及其下游分解代谢因子(MMP3, MMP13,ADAMTs-4)的表达相应增加(P<0.05)。结论 超负荷压力激活HIF-2α,继而激活下游分解代谢因子可能是导致髁突软骨损伤的一个机制。

关键词: 低氧诱导因子-2α, 分解代谢因子, 低氧培养, 应力加载, 髁突软骨

Abstract: Abstract: Objective To explore the expression of HIF-2α and its downstream catabolic factors (MMP3, MMP13, ADAMTs-4) in the mandibular condyle chondrocytes (MCC) under different stress loadings. Methods The third generation of MCC were cultured in 5% hypoxia. The uniaxial pressure of 0,1000,2000,4000 units strain (ust) were exerted on the MCC for 2 h. Then the specimens were collected and dyed by trypan blue staining. The morphology and number of cells were observed under a light microscope, and the cell mortality was calculated. Westernblot and RTPCR were performed to detect the changes of expression of HIF-2α and its downstream catabolic factors (MMP3, MMP13, ADAMTs-4). Results With the increase of pressure, the cell mortality increased (P<0.05). The expression of HIF-2α and its downstream catabolic factors (MMP3, MMP13, ADAMTs-4) increased with the increase of pressure (P<0.05). Conclusion The activation of HIF-2α and its downstream catabolic factors by overload pressure may be responsible for the damage of condyle chondrocytes.

Key words: HIF-2α, Catabolic factor, Hypoxia, Stress loading, Condyle chondrocyte

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