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首页> 外文期刊>Inflammation research: Official journal of the European Histamine Research Society >Hydrogen peroxide induces apoptosis of chondrocytes; involvement of calcium ion and extracellular signal-regulated protein kinase.
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Hydrogen peroxide induces apoptosis of chondrocytes; involvement of calcium ion and extracellular signal-regulated protein kinase.

机译:过氧化氢诱导软骨细胞凋亡;钙离子和细胞外信号调节蛋白激酶的参与。

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OBJECTIVE: Recent observations demonstrated that reactive oxygen species facilitate cartilage degradation. We demonstrated that hydrogen peroxide (H2O2) caused inhibition of proteoglycan synthesis, induction of apoptosis and stimulation of extracellular signal-regulated protein kinase (ERK) of the chondrocytes (Inflamm Res 48: 399-403, 1999). To determine whether activation of ERK is involved in the induction of chondrocyte apoptosis, we examined the signal transduction pathways in this hydrogen peroxide induced apoptosis. DESIGN: Bovine articular chondrocytes were cultured. To determine the induction of apoptosis, Annexin V staining and terminal deoxynucleotidyl transferase were used. The activity of caspase-3 was measured using an apopain assay kit. Intracellular Ca2+ imaging was observed after fura2-AM loading. RESULTS: Hydrogen peroxide enhanced annexin V positive apoptotic cells and caspase-3 activity, which is an executor of apoptosis. Hydrogen peroxide also enhanced intracellular Ca2+ and preincubation with the intracellular Ca2+ chelator protected chondrocytes against hydrogen peroxide-induced cell apoptosis, indicating that an increase in the cytosolic Ca2+ plays a decisive role in this action. When ERK activity was blocked with geldanamycin and PD098059, increased apoptosis was evident. CONCLUSION: Hydrogen peroxide induces chondrocyte apoptosis via Ca2+ signaling, and ERK is involved in these signal transduction pathways.
机译:目的:最近的观察表明,活性氧促进软骨降解。我们证明过氧化氢(H2O2)抑制软骨蛋白聚糖合成,诱导凋亡和刺激软骨细胞的细胞外信号调节蛋白激酶(ERK)(Inflamm Res 48:399-403,1999)。为了确定ERK的激活是否参与软骨细胞凋亡的诱导,我们检查了这种过氧化氢诱导的细胞凋亡中的信号转导途径。设计:培养牛关节软骨细胞。为了确定凋亡的诱导,使用膜联蛋白V染色和末端脱氧核苷酸转移酶。使用Apopain分析试剂盒测量caspase-3的活性。 fura2-AM加载后观察到细胞内Ca2 +成像。结果:过氧化氢增强了膜联蛋白V阳性凋亡细胞和caspase-3的活性,这是凋亡的执行者。过氧化氢还增强了细胞内Ca2 +,并与细胞内Ca2 +螯合剂预孵育保护了软骨细胞免受过氧化氢诱导的细胞凋亡,表明胞质Ca2 +的增加在该作用中起决定性作用。当格尔德霉素和PD098059阻断ERK活性时,细胞凋亡明显增加。结论:过氧化氢通过Ca 2+信号传导诱导软骨细胞凋亡,而ERK参与这些信号传导途径。

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