Allen W K, Akeson R
J Neurosci. 1985 Feb;5(2):284-96. doi: 10.1523/JNEUROSCI.05-02-00284.1985.
A monoclonal antibody (Mab) has been developed which recognizes a family of cell surface glycoproteins found in high levels of rat olfactory receptor neurons. This Mab, designated 2B8, was produced by the fusion of X63-Ag8.653 myeloma cells and spleen cells of a mouse immunized with PC12 rat pheochromocytoma cells. Immunofluorescence analyses of cryostat sections of neonatal olfactory epithelium show prominent 2B8 binding to receptor neurons. Within the olfactory bulb only the glomerular and olfactory nerve layers show 2B8 binding. All other neural structures in the main olfactory bulb have background levels of reactivity. Analyses of 2B8 binding to particulate protein preparations from several central and peripheral nervous system components demonstrated highest 2B8 antigen specific activity in olfactory bulb and epithelium and detectable levels in dorsal root ganglia (DRG), whole cerebrum, cerebellum, and brainstem. However, 2B8 antigen could not be detected in non-olfactory structures by immunofluorescence. Some non-neural tissues also had the ability to bind 2B8 Mab in the particulate protein radioimmunoassay. In order to compare the 2B8-reactive molecules found in each tissue, Mab was applied to polyacrylamide gels of unlabeled membrane proteins. A family of molecules with diverse molecular weights was found. Some were unique to individual tissues whereas others were shared among tissues. Olfactory bulb and epithelium had a unique band with Mr = 215,000 and another band with Mr = 142,000. The 142,000-dalton band was also found with PC12 cells. PC12 cells also had several bands of lesser molecular weight, including 51,000 and 43,000. Testes membranes had immunoreactive bands only at Mr = 46,000 and 43,000. Bone marrow, perinatal liver, and DRG each expressed a single 2B8-reactive band with Mr = approximately 114,000. Salivary gland had four reactive bands, two common to it and only PC12 cells, the 114,000-dalton band which is similar to that found in adult rat bone marrow and DRG, and a unique band at Mr = 152,000. 2B8 immunoprecipitates of olfactory bulb and epithelium were analyzed for glycosyl groups by lectin reactivity. Wheat germ agglutinin and Ricinus communus agglutinin I bound the 2B8 antigens using two distinct assay methods. This suggests that the 2B8 antigens recognized in the olfactory system are glycoproteins having sialic acid and D-galactosyl components.(ABSTRACT TRUNCATED AT 400 WORDS)
已研发出一种单克隆抗体(Mab),它可识别在大鼠嗅觉受体神经元中高表达的一类细胞表面糖蛋白。这种名为2B8的单克隆抗体是由X63 - Ag8.653骨髓瘤细胞与用PC12大鼠嗜铬细胞瘤细胞免疫的小鼠脾细胞融合产生的。对新生小鼠嗅觉上皮冷冻切片的免疫荧光分析显示,2B8与受体神经元有显著结合。在嗅球内,只有肾小球层和嗅神经层显示2B8结合。主嗅球中的所有其他神经结构的反应性处于背景水平。对来自几个中枢和外周神经系统成分的颗粒状蛋白质制剂进行2B8结合分析表明,2B8抗原特异性活性在嗅球和上皮中最高,在背根神经节(DRG)、全脑、小脑和脑干中可检测到。然而,通过免疫荧光在非嗅觉结构中未检测到2B8抗原。在颗粒状蛋白质放射免疫分析中,一些非神经组织也有结合2B8单克隆抗体的能力。为了比较在每个组织中发现的与2B8反应的分子,将单克隆抗体应用于未标记膜蛋白的聚丙烯酰胺凝胶。发现了一系列分子量不同的分子。有些是个别组织特有的,而有些则在组织间共享。嗅球和上皮有一条Mr = 215,000的独特条带和另一条Mr = 142,000的条带。在PC12细胞中也发现了142,000道尔顿的条带。PC12细胞还有几条分子量较小的条带,包括51,000和43,000。睾丸膜的免疫反应条带仅在Mr = 46,000和43,000处。骨髓、围产期肝脏和DRG各自表达一条Mr约为114,000的单一2B8反应条带。唾液腺有四条反应条带,两条是它和PC12细胞共有的,114,000道尔顿的条带与成年大鼠骨髓和DRG中的相似,还有一条Mr = 152,000的独特条带。通过凝集素反应性分析嗅球和上皮的2B8免疫沉淀物中的糖基。麦胚凝集素和蓖麻凝集素I使用两种不同的检测方法结合2B8抗原。这表明在嗅觉系统中识别的2B8抗原是具有唾液酸和D - 半乳糖基成分的糖蛋白。(摘要截短至400字)