Shiomura Y, Hirokawa N
Department of Anatomy and Cell Biology, School of Medicine, University of Tokyo, Japan.
Brain Res. 1989 Nov 20;502(2):356-64. doi: 10.1016/0006-8993(89)90632-x.
A novel microtubule associated protein (MAP) was identified with a monoclonal antibody (mAb) among rat brain microtubule (MT) proteins. This MAP, which is found in a heat-stable MAP fraction, is co-polymerized with tubulin from rat brain homogenates both in cycled and in taxol-driven assembly purifications. When the heat-stable fraction of MT proteins and purified tubulin are assembled in vitro without taxol, 205 kDa MAP is identified in the MT pellet. Immunofluorescent studies using the mAb against this MAP on sections of a rat spinal cord, hippocampus, retina and cerebellar cortex, showed that 205 kDa MAP was localized in not only neural cell bodies, dendrites, and axons, but also in glial cells. This 205 kDa MAP is clearly distinct from previously reported MAPs as to molecular mass, heat stability, immunoreactivity, distribution among tissues or within a neuron, and the developmental aspect of the postnatal cerebellar cortex. As for development, the 205 kDa MAP has already been seen to appear at postnatal day 3. Throughout the postnatal development of the cerebellar cortex, 205 kDa MAP is expressed in developing Purkinje cells, with the staining reaction being particularly intense in the more superficially positioned parallel fiber profiles. This points out the possible important functions of 205 kDa MAP in the morphogenesis of parallel fiber axons.
在大鼠脑微管(MT)蛋白中,通过单克隆抗体(mAb)鉴定出一种新型微管相关蛋白(MAP)。这种MAP存在于热稳定的MAP组分中,在循环组装和紫杉醇驱动的组装纯化过程中,均与大鼠脑匀浆中的微管蛋白共聚合。当MT蛋白的热稳定组分和纯化的微管蛋白在无紫杉醇的情况下进行体外组装时,在MT沉淀中可鉴定出205 kDa的MAP。使用针对这种MAP的mAb对大鼠脊髓、海马、视网膜和小脑皮质切片进行免疫荧光研究,结果显示205 kDa的MAP不仅定位于神经细胞体、树突和轴突,还定位于神经胶质细胞。这种205 kDa的MAP在分子量、热稳定性、免疫反应性、组织间或神经元内的分布以及出生后小脑皮质的发育方面,均与先前报道的MAP明显不同。关于发育,在出生后第3天即可观察到205 kDa的MAP出现。在小脑皮质的整个出生后发育过程中,205 kDa的MAP在发育中的浦肯野细胞中表达,在位置较浅的平行纤维区域染色反应尤为强烈。这表明205 kDa的MAP在平行纤维轴突的形态发生中可能具有重要功能。