Matsuoka I, Satake R, Kurihara K
Brain Res. 1986 Jan;389(1-2):133-43. doi: 10.1016/0165-3806(86)90181-1.
Culture medium conditioned over C6 glioma cells (GCM) contains factors which induce neurite outgrowth from clonal rat pheochromocytoma (PC12) cells. The effects of GCM on the cell-substratum adhesion of PC12 cells, which is an early event required for the neurite outgrowth, were investigated. The results obtained are as follows. Addition of GCM promoted the adhesion of PC12 cells specifically to collagen-coated tissue culture dish. The GCM-promoted adhesion of PC12 cells was prevented by the treatment of the cells with cytochalasin B, concanavalin A and glycosidase mixture suggesting the contribution of microfilaments and cell surface carbohydrates in the cell adhesion. GCM did not increase significantly the intracellular content of cAMP and the extent of cell adhesion promoted by cAMP or dibutyryl-cAMP was much less than that by GCM. Two active factors contained in GCM were separated by either gel filtration or chromatofocusing using the cell adhesion assay as an index. The first factor with an apparent mol. wt. around 40,000 had the abilities to induce the neurite outgrowth and to enhance the choline acetyltransferase activity in addition to the ability to promote the adhesion of PC12 cells. The second factor with an apparent mol. wt. around 10,000 was devoid of the ability to induce the neurite outgrowth, but had the abilities to enhance the choline acetyltransferase activity and to promote the adhesion of PC12 cells. Both factors were sensitive to trypsin digestion and relatively heat stable. The significance of these factors in the neuronal differentiation was discussed.
经C6胶质瘤细胞处理的条件培养基(GCM)含有能诱导克隆大鼠嗜铬细胞瘤(PC12)细胞长出神经突的因子。研究了GCM对PC12细胞与底物黏附的影响,这是神经突生长所需的早期事件。所得结果如下。添加GCM可促进PC12细胞特异性黏附于胶原包被的组织培养皿。用细胞松弛素B、伴刀豆球蛋白A和糖苷酶混合物处理细胞可阻止GCM促进的PC12细胞黏附,提示微丝和细胞表面碳水化合物在细胞黏附中起作用。GCM并未显著增加细胞内cAMP含量,且cAMP或二丁酰-cAMP促进的细胞黏附程度远低于GCM。以细胞黏附试验为指标,通过凝胶过滤或色谱聚焦法分离了GCM中所含的两种活性因子。第一种因子表观分子量约为40,000,除了具有促进PC12细胞黏附的能力外,还具有诱导神经突生长和增强胆碱乙酰转移酶活性的能力。第二种因子表观分子量约为10,000,缺乏诱导神经突生长的能力,但具有增强胆碱乙酰转移酶活性和促进PC12细胞黏附的能力。两种因子均对胰蛋白酶消化敏感且相对耐热。讨论了这些因子在神经元分化中的意义。