Matsuda Y, Okitsu A, Sato S, Koito H, Yamamoto H
Department of Immunology, National Institute of Neuroscience, Tokyo, Japan.
Neurosci Lett. 1996 Feb 23;205(2):87-90. doi: 10.1016/0304-3940(96)12381-8.
A soluble chimera protein consisting of the extracellular region of mouse myelin-associated glycoprotein (MAG) and the Fc region of human immunoglobulin G1, MAG-IgG, was prepared by transfecting an expression vector, BCMGSneo, containing the corresponding fused gene into mouse myeloma P3U1 cells. It was found that this MAG derivative promoted neurite growth of mouse cerebellar neurons in culture. In the presence of MAG-IgG the rates of neurite-bearing cells were significantly increased, and the neurites were distinctly lengthened. It was also observed that the anti-MAG monoclonal antibody inhibited this stimulation of neurite extension, supporting the specificity of the effect of MAG-IgG. These results suggest that soluble MAG derivative might act as a neurotrophic factor in the developing brain.
通过将含有相应融合基因的表达载体BCMGSneo转染到小鼠骨髓瘤P3U1细胞中,制备了一种可溶性嵌合蛋白,其由小鼠髓鞘相关糖蛋白(MAG)的细胞外区域和人免疫球蛋白G1的Fc区域组成,即MAG-IgG。研究发现,这种MAG衍生物可促进培养的小鼠小脑神经元的神经突生长。在存在MAG-IgG的情况下,有神经突的细胞比例显著增加,且神经突明显延长。还观察到抗MAG单克隆抗体抑制了这种对神经突延伸的刺激作用,这支持了MAG-IgG作用的特异性。这些结果表明,可溶性MAG衍生物可能在发育中的大脑中充当神经营养因子。