Burger M, Hess M W, Cottier H
Immunol Lett. 1986 Mar;12(2-3):121-5. doi: 10.1016/0165-2478(86)90093-3.
The proliferation of mouse spleen cells and T-lymphocytes, initiated by the calcium ionophore A 23187 was studied by a serum-free culture technique. In contrast to Con A, A 23187 was capable of stimulating cells only if 2-mercaptoethanol, cysteine and glutathione (reduced form), respectively, were present in the culture medium. In the absence of one of these compounds a stimulating activity of A 23187 was observed only with high concentrations of cells (i.e., 10(7)/ml). With glutathione present, the cells could be stimulated only at concentrations of A 23187 which were found to be suboptimal in cultures with 2-mercaptoethanol. Human serum, fetal calf serum and bovine serum albumin shifted the active and optimally stimulating concentrations of A 23187 to higher values. A similar effect was observed with sera- and Con A-treated cells. The effect of sera and albumin was paralleled by a protecting effect of cells against high concentrations of A 23187.
采用无血清培养技术研究了钙离子载体A 23187引发的小鼠脾细胞和T淋巴细胞增殖情况。与刀豆蛋白A不同,只有当培养基中分别存在2-巯基乙醇、半胱氨酸和谷胱甘肽(还原型)时,A 23187才有能力刺激细胞。若缺少其中一种化合物,只有在高细胞浓度(即10⁷/ml)时才观察到A 23187的刺激活性。有谷胱甘肽存在时,只有在A 23187浓度低于含2-巯基乙醇培养中的最适浓度时,细胞才能被刺激。人血清、胎牛血清和牛血清白蛋白会使A 23187的活性和最佳刺激浓度升高。在经血清和刀豆蛋白A处理的细胞中也观察到类似效果。血清和白蛋白的作用与细胞对高浓度A 23187的保护作用相似。