Chandler C E, Parsons L M, Hosang M, Shooter E M
J Biol Chem. 1984 Jun 10;259(11):6882-9.
A nerve growth factor (NGF) receptor interactive monoclonal antibody (192-IgG) which enhances beta-NGF binding to PC12 cells has been produced. The hybridoma clone was obtained by fusing Sp2/0- Ag14 myeloma cells with splenocytes from Balb/C mice which had been immunized with n-octyl glucoside solubilized proteins from isolated PC12 cell plasma membranes. The antibody is an IgG, which does not bind beta-NGF. It binds to the same number of sites on PC12 cells at low temperature as does beta-NGF. The 192-IgG increases the apparent affinity of beta-NGF binding to fast receptors on PC12 cells at low temperature by a factor of 2.5- to 4-fold and enhances the photoactivatable cross-linking of beta-NGF to the same receptor while decreasing the cross-linking of beta-NGF to the slow NGF receptor. At 37 degrees C 192-IgG partially inhibits the regeneration of neurites from primed PC12 cells. The 192-IgG also reduces the rate of appearance of binding to slow NGF receptors and increases the proportion of beta-NGF bound to fast receptors at 37 degrees C. These results implicate the slow receptor as the mediator of the biological response. This antibody provides a tool for examining steps in the mechanism of action of beta-NGF after binding to the receptor.
已制备出一种增强β-神经生长因子(NGF)与PC12细胞结合的神经生长因子(NGF)受体相互作用单克隆抗体(192-IgG)。该杂交瘤克隆是通过将Sp2/0-Ag14骨髓瘤细胞与来自用从分离的PC12细胞质膜中用正辛基葡糖苷溶解的蛋白质免疫的Balb/C小鼠的脾细胞融合而获得的。该抗体是一种IgG,不与β-NGF结合。在低温下,它与PC12细胞上相同数量的位点结合,与β-NGF相同。192-IgG在低温下将β-NGF与PC12细胞上快速受体结合的表观亲和力提高了2.5至4倍,并增强了β-NGF与同一受体的光可活化交联,同时减少了β-NGF与慢速NGF受体的交联。在37℃时,192-IgG部分抑制预致敏的PC12细胞神经突的再生。192-IgG还降低了与慢速NGF受体结合的出现速率,并在37℃时增加了与快速受体结合的β-NGF的比例。这些结果表明慢速受体是生物学反应的介导者。该抗体为研究β-NGF与受体结合后作用机制的步骤提供了一种工具。