Vincent F, Brun H, Clain E, Ronot X, Adolphe M
Laboratoire de Pharmacologie Cellulaire de I'E.P.H.E., Institut Biomédical des Cordeliers, Paris, France.
J Cell Physiol. 1989 Nov;141(2):262-6. doi: 10.1002/jcp.1041410205.
It can be postulated that among the factors implicated in cartilaginous lesions, oxygen-derived free radicals seem to have a prominent part. To investigate this hypothesis, rabbit articular chondrocyte cultures have been exposed to oxygen-derived reactive species generated by the hypoxanthine-xanthine oxydase system. We observed a dose-dependent decrease of cellular growth. In order to explain this result, cell cycle progression and binucleate cell fractions have been studied. A greater number of binucleate cells and an increase in cell volume were observed. Flow cytometry analysis revealed a perturbation in cell cycle progression leading to a significant increase in the proportion of cells in G2 phase and an important augmentation in cell protein content confirmed by biochemical assays. This model shows which type of alteration can be induced by oxygen-derived free radicals in vitro. In addition, we deem this model to be useful for studying degenerative processes and for screening drugs that can scavenge oxygen-free radicals.
可以推测,在与软骨损伤有关的因素中,氧衍生的自由基似乎起着重要作用。为了研究这一假设,兔关节软骨细胞培养物已暴露于由次黄嘌呤-黄嘌呤氧化酶系统产生的氧衍生反应性物质中。我们观察到细胞生长呈剂量依赖性下降。为了解释这一结果,对细胞周期进程和双核细胞比例进行了研究。观察到双核细胞数量增加且细胞体积增大。流式细胞术分析显示细胞周期进程受到干扰,导致G2期细胞比例显著增加,生化分析证实细胞蛋白质含量也有重要增加。该模型显示了氧衍生自由基在体外可诱导哪种类型的改变。此外,我们认为该模型对于研究退行性过程以及筛选可清除氧自由基的药物是有用的。