Stainier D Y, Gilbert W
Department of Cellular and Developmental Biology, Harvard University, Cambridge, Massachusetts 02138.
J Neurosci. 1989 Jul;9(7):2468-85. doi: 10.1523/JNEUROSCI.09-07-02468.1989.
A monoclonal antibody, B30, obtained with whole cells from embryonic brain as an immunogen, recognizes a neuronal cell surface antigen that appears only in 2 distinct systems in the developing mouse brain: the trigeminal system and the cerebellum. In the trigeminal system, B30 labels the surface of neurons, including their axons and their transient dendrites, in 2 groups of cells: the centrally located mesencephalic trigeminal nucleus and the peripheral trigeminal ganglion. Immunoreactivity is detectable during axon outgrowth, peaks around the seventh postnatal day, and disappears around 2 weeks after birth. In the cerebellum, B30 labels 2 layers of cells during development. Perinatally, and for about a week after birth, the layer of premigratory granule cells stains. After their maturation, Purkinje cells start to stain and by 12 d postnatally all the Purkinje cell bodies, their axons, and their dendritic trees show strong immunoreactivity. Subsequently, and in the adult, this staining is lost from some cells to reveal bands of antigen positive and negative Purkinje cells. Initial biochemical characterization of the epitope shows that it is carried on 2 minor gangliosides.
一种单克隆抗体B30,以胚胎脑全细胞作为免疫原获得,可识别一种神经元细胞表面抗原,该抗原仅在发育中的小鼠脑中的两个不同系统中出现:三叉神经系统和小脑。在三叉神经系统中,B30标记两组细胞中神经元的表面,包括它们的轴突和短暂的树突:位于中枢的中脑三叉神经核和外周三叉神经节。在轴突生长期间可检测到免疫反应性,在出生后第7天左右达到峰值,并在出生后约2周消失。在小脑中,B30在发育过程中标记两层细胞。在围产期以及出生后约一周,迁移前颗粒细胞层染色。它们成熟后,浦肯野细胞开始染色,到出生后12天,所有浦肯野细胞体、它们的轴突和树突都显示出强烈的免疫反应性。随后,在成年期,一些细胞失去这种染色,从而显示出抗原阳性和阴性浦肯野细胞带。该表位的初步生化特征表明它存在于两种次要神经节苷脂上。