Stallcup W B, Beasley L
J Neurosci. 1987 Sep;7(9):2737-44. doi: 10.1523/JNEUROSCI.07-09-02737.1987.
We have studied the expression of the NG2 chondroitin sulfate proteoglycan on bipotential glial precursor cells in cultures of postnatal rat optic nerve. Purified populations of these precursor cells were prepared by panning dissociated optic nerve cells on dishes coated with monoclonal A2B5 antibody. Using immunofluorescence double staining, we found that NG2 was present on almost 95% of the purified A2B5+ precursor cells. The NG2 core protein from optic nerve cells was identified by immune precipitation and PAGE and was found to be identical to the 300,000 Da NG2 core protein from a clonal rat cell line B49. Over a culture period of 5 d in medium containing 10% fetal calf serum, more than 80% of the NG2+ precursor cells acquired the glial fibrillary acidic protein (GFAP), an astrocyte-specific marker. Under these conditions, fewer than 10% of the NG2+ cells expressed galactocerebroside (GC), an oligodendrocyte-specific marker. These GFAP+GC- type II astrocytes continued to express the NG2 antigen for up to 10 d in culture. During a 5 d culture period in hormonally supplemented, serum-free medium, fewer than 15% of the NG2+ cells expressed GFAP, while up to 40% expressed GC. The NG2 antigen continued to be expressed for only a short period of time by these GFAP-GC+ oligodendrocytes, so that mature oligodendrocytes in the cultures became NG2-. These results support our previous suggestion that the NG2 antigen is found on a class of neural cells that can differentiate along more than one pathway.
我们研究了硫酸软骨素蛋白聚糖NG2在新生大鼠视神经培养物中的双潜能神经胶质前体细胞上的表达。通过将解离的视神经细胞铺在包被有单克隆抗体A2B5的培养皿上,制备了这些前体细胞的纯化群体。利用免疫荧光双重染色,我们发现几乎95%的纯化A2B5 +前体细胞上存在NG2。通过免疫沉淀和聚丙烯酰胺凝胶电泳鉴定了来自视神经细胞的NG2核心蛋白,发现其与来自克隆大鼠细胞系B49的300,000 Da的NG2核心蛋白相同。在含有10%胎牛血清的培养基中培养5天的过程中,超过80%的NG2 +前体细胞获得了胶质纤维酸性蛋白(GFAP),这是一种星形胶质细胞特异性标志物。在这些条件下,少于10%的NG2 +细胞表达半乳糖脑苷脂(GC),这是一种少突胶质细胞特异性标志物。这些GFAP + GC - II型星形胶质细胞在培养中持续表达NG2抗原长达10天。在添加激素的无血清培养基中培养5天的过程中,少于15%的NG2 +细胞表达GFAP,而高达40%的细胞表达GC。这些GFAP - GC +少突胶质细胞仅在短时间内持续表达NG2抗原,因此培养物中的成熟少突胶质细胞变为NG2 -。这些结果支持了我们之前的推测,即在一类可沿多条途径分化的神经细胞上发现了NG2抗原。