Fitzsimmons R J, Ryaby J T, Mohan S, Magee F P, Baylink D J
Department of Medicine, Loma Linda University, Jerry L. Pettis VA Hospital, California 92354, USA.
Endocrinology. 1995 Jul;136(7):3100-6. doi: 10.1210/endo.136.7.7789337.
In vitro exposure to low-energy, combined magnetic fields (CMF) increased the release of insulin-like growth factor (IGF)-II from human TE-85 osteosarcoma cells. Short-term CMF exposure of only 10 min increased IGF-II levels in conditioned medium 1 h post CMF exposure. IGF-II levels were measured with a radioreceptor assay using H-35 cells that contain abundant IGF-II but not IGF-I receptors. This assay also uses a recently validated BioGel P-10 acid gel filtration method to remove IGF binding protein before quantitation of either IGF-I or IGF-II. In addition to an increase in IGF-II levels, DNA synthesis, as an index of cell proliferation, was increased during the 24-h period post CMF exposure. A monoclonal antibody against IGF-II blocked the increase in cell proliferation following CMF exposure, whereas a control monoclonal antibody against osteocalcin did not attenuate the mitogenic action of CMF exposure. The effect of CMF exposure to increase both cell proliferation and IGF-II was cell-density dependent with greater stimulation by CMF observed at lower densities. Together, these data are consistent with the hypothesis that CMF exposure stimulates release/production of IGF-II from bone cells and that increased IGF-II then promotes an increase in cell proliferation.
体外暴露于低能量复合磁场(CMF)可增加人TE - 85骨肉瘤细胞中胰岛素样生长因子(IGF)-II的释放。仅10分钟的短期CMF暴露可在CMF暴露后1小时增加条件培养基中的IGF-II水平。使用含有丰富IGF-II但不含IGF-I受体的H-35细胞通过放射受体测定法测量IGF-II水平。该测定法还使用最近验证的BioGel P-10酸性凝胶过滤方法在定量IGF-I或IGF-II之前去除IGF结合蛋白。除了IGF-II水平增加外,作为细胞增殖指标的DNA合成在CMF暴露后的24小时内增加。抗IGF-II单克隆抗体可阻断CMF暴露后细胞增殖的增加,而抗骨钙素对照单克隆抗体则不会减弱CMF暴露的促有丝分裂作用。CMF暴露增加细胞增殖和IGF-II的作用呈细胞密度依赖性,在较低密度下观察到CMF的刺激作用更强。总之,这些数据与以下假设一致:CMF暴露刺激骨细胞释放/产生IGF-II,而增加的IGF-II随后促进细胞增殖增加。