Goodman M G, Weigle W O
J Immunol. 1978 May;120(5):1453-9.
Recent evidence has indicated that addition of 2-mercaptoethanol (2-ME) to culture medium is able to activate murine lymphocytes to undergo blastogenesis, to synthesize polyclonal antibody, and to develop cytotoxicity to both autologous and heterologous target cells. In order to explore the basis for these phenomena, a study of the physical interaction between the cell and 2-ME was undertaken by using a radiolabeled preparation of 2-ME. Uptake of labeled 2-ME increased over the initial 24 hr of culture, after which a steady state was achieved. Cells were found to have maximal susceptibility to activation by 2-ME after incubation for 24 hr in the absence of the thiol compound. This observation was not explicable in terms of any alteration in the kinetics of 2-ME uptake. The amount of labeled 2-ME taken up was a function of the 2-ME concentration with which the cell was incubated, with the exception of the concentration range that is optimal for mitogenesis. At this range, the curve was suggestive of a saturation effect. Uptake by B cell cultures was found to exceed that by T cell cultures. Uptake was shown to result from interaction with protein, to be independent of metabolic energy, to be governed by temperature-dependent kinetics, and to be highly specific.
最近的证据表明,在培养基中添加2-巯基乙醇(2-ME)能够激活小鼠淋巴细胞,使其发生细胞增殖、合成多克隆抗体,并对自体和异源靶细胞产生细胞毒性。为了探究这些现象的基础,使用放射性标记的2-ME制剂对细胞与2-ME之间的物理相互作用进行了研究。在培养的最初24小时内,标记的2-ME摄取量增加,之后达到稳定状态。发现在不存在硫醇化合物的情况下孵育24小时后,细胞对2-ME激活具有最大敏感性。就2-ME摄取动力学的任何改变而言,这一观察结果无法解释。摄取的标记2-ME量是细胞孵育时2-ME浓度的函数,但有丝分裂原形成的最佳浓度范围除外。在此范围内,曲线提示存在饱和效应。发现B细胞培养物的摄取量超过T细胞培养物。已表明摄取是由与蛋白质的相互作用引起的,与代谢能量无关,受温度依赖性动力学支配,且具有高度特异性。