Acta Chimica Sinica ›› 2011, Vol. 69 ›› Issue (03): 284-290. Previous Articles     Next Articles

Full Papers

非洲绿猴肾上皮细胞的损伤模型及其对草酸钙生长的调控作用

张生,杨如娥,欧阳健明*   

  1. (暨南大学生物矿化与结石病防治研究所 广州 510632)
  • 投稿日期:2010-05-08 修回日期:2010-07-10 发布日期:2010-09-20
  • 通讯作者: 欧阳健明 E-mail:toyjm@jnu.edu.cn
  • 基金资助:

    细胞调控草酸钙生物矿化的分子机制

Injury Model of African Green Monkey Kidney Epithelial Cell and Its Modulation on Calcium Oxalate Formation

ZHANG Sheng, YANG Ru-E, OUYang-Jian-Ming   

  1. (Institute of Biomineralization and Lithiasis Research, Jinan University, Guangzhou 510632)
  • Received:2010-05-08 Revised:2010-07-10 Published:2010-09-20

H2O2 was used to injure African green monkey renal epithelial cells (Vero). The injury degree of Vero cells was characterized by detecting the cell survival rate, the concentration change of superoxide dismutase (SOD) in culture medium, the release of malondialdehyde (MDA) and the change of expression quantity of osteopontin (OPN) on cellular surface. The injured degree of Vero cells by H2O2 was time-dependent and concentration-dependent. After injured, the release quantity of MDA increased, the concentration of SOD decreased and the expression quantity of OPN increased significantly, thus resulting in an increase of the adherent quantity of crystals. The modulation of cells before and after injury to the growth of calcium oxalate (CaOxa) crystals was investigated by scanning electron microscopy (SEM) and X-ray diffraction (XRD). The CaOxa crystals induced by the cells in control group contained simultaneously calcium oxalate monohydrate (COM) and dihydrate (COD) crystals, and these crystals had obtuse edges and corners. However, the crystals induced by the cells in injured group were mainly COM crystals, and they had irregular shape with sharp edges and corners. Consequently, the risk of CaOxa stones formation increased after the cells were injured. The oxidative injury model of Vero cells established in this paper was in favor of understanding the formation mechanism of calcium oxalate stones in cell level.

Key words: biomineralization, calcium oxalate, cell modulation, oxidative damage