Heredia M, Gascuel J, Ramón-Cueto A, Santacana M, Avila J, Masson C, Valverde F
Departamento Fisiología y Farmacología, Facultad de Medicina, Universidad de Salamanca, Spain.
Glia. 1998 Nov;24(3):352-64. doi: 10.1002/(sici)1098-1136(199811)24:3<352::aid-glia10>3.0.co;2-y.
We produced and characterized two monoclonal antibodies, termed 1.9.E and 4.11.C, that specifically recognize olfactory bulb ensheathing glia. Both antibodies were generated using the olfactory nerve layer (ONL) of newborn rat olfactory bulbs (P0, P1) as immunogens. The specificity of these antibodies was tested by immunofluorescence techniques on tissue sections and cultures of adult and neonatal rat olfactory bulbs, and by Western blot analysis. 1.9.E labeled the ONL and glomerular layer of the olfactory bulb (OB) of adult rats. In newborn rats, 1.9.E immunostained ensheathing cells from the ONL and peripheral olfactory fascicles. Furthermore, 1.9.E reacted with some processes of the radial glia in the periventricular germinal layer of the newborn rat. Although 4.11.C also specifically labeled ensheathing cells in the adult OB, it did not stain any cell type in the ONL of newborn rats. The lack of double labeling with either 1.9.E or 4.11.C and anti-olfactory marker protein (OMP) antibody, a specific marker for olfactory axons, indicated that none of the monoclonals recognized olfactory axons. Double immunostaining of adult OB cultures with 1.9.E or 4.11.C and anti-p75-nerve growth factor receptor revealed that both antibodies specifically recognized ensheathing glia in those cultures. Filaments were strongly labeled throughout the entire cytoplasm of ensheathing cells, suggesting that 1.9.E and 4.11.C immunoreacted with ensheathing glia cytoskeleton. 4.11.C stained a few Schwann cells in adult sciatic nerve sections. Moreover, 4.11.C immunostained cortical astrocyte cultures from newborn rats (P1). In Western blot analysis both antibodies recognized a major component, migrating with an apparent molecular weight of 60 kDa, from olfactory nerve and glomerular layer (ONGL) extracts of adult and neonatal rats. The pattern of immunoreactivity of 1.9.E and 4.11.C antibodies suggest that both antibodies are specific markers for olfactory ensheathing glia in the adult rat central nervous system (CNS).
我们制备并鉴定了两种单克隆抗体,分别命名为1.9.E和4.11.C,它们能特异性识别嗅球被膜胶质细胞。这两种抗体均以新生大鼠(出生后0天、1天)嗅球的嗅神经层(ONL)作为免疫原产生。通过免疫荧光技术对成年和新生大鼠嗅球的组织切片及培养物进行检测,并通过蛋白质免疫印迹分析,来测试这些抗体的特异性。1.9.E标记成年大鼠嗅球(OB)的嗅神经层和肾小球层。在新生大鼠中,1.9.E免疫染色嗅神经层和外周嗅束的被膜细胞。此外,1.9.E与新生大鼠脑室周围生发层的放射状胶质细胞的一些突起发生反应。虽然4.11.C也能特异性标记成年嗅球中的被膜细胞,但它不能对新生大鼠嗅神经层中的任何细胞类型进行染色。1.9.E或4.11.C与抗嗅觉标记蛋白(OMP)抗体(一种嗅轴突的特异性标记物)均未出现双重标记,这表明这些单克隆抗体均不能识别嗅轴突。用1.9.E或4.11.C与抗p75神经生长因子受体对成年嗅球培养物进行双重免疫染色,结果显示这两种抗体均能在这些培养物中特异性识别被膜胶质细胞。在被膜细胞的整个细胞质中,细丝均被强烈标记,这表明1.9.E和4.11.C与被膜胶质细胞的细胞骨架发生了免疫反应。4.11.C对成年坐骨神经切片中的一些雪旺细胞进行了染色。此外,4.11.C对新生大鼠(出生后1天)的皮质星形胶质细胞培养物进行了免疫染色。在蛋白质免疫印迹分析中,这两种抗体均识别出成年和新生大鼠嗅神经和肾小球层(ONGL)提取物中的一种主要成分,其表观分子量为60 kDa。1.9.E和4.11.C抗体的免疫反应模式表明,这两种抗体都是成年大鼠中枢神经系统(CNS)中嗅球被膜胶质细胞的特异性标记物。