Burchiel S W, Warner N L
J Immunol. 1980 Mar;124(3):1016-21.
Cyclic AMP-elevating agents have been shown to increase the expression of Fc receptors on the Abelson virus-induced pre-B cell tumor ABE-8. Such agents included isoproterenol, PGE1, 3-isobutyl-1-methyl xanthine, and 8 BrcAMP. The positive inductive effect produced by these agents was inhibited by 8 BrcGMP and PGF2 alpha, which putatively elevate cyclic GMP levels. Other agents also shown to induce Fc receptor expression were LPS and certain batches of fetal calf sera. In contrast to the inductive effect produced by cyclic AMP elevating agents, 8 BrcGMP and PGF2 alpha were unable to reverse the increased Fc receptor expression produced by LPS and fetal calf sera. Thus, these latter agents may act via a qualitatively different mechanism in producing a change in phenotypic expression. The results of this study are discussed in terms of the use of tumor cells as a model system for studying the pharmacologic control of lymphocyte differentiation.
环磷酸腺苷(cAMP)升高剂已被证明可增加阿贝尔森病毒诱导的前B细胞肿瘤ABE - 8上Fc受体的表达。这类试剂包括异丙肾上腺素、前列腺素E1、3 - 异丁基 - 1 - 甲基黄嘌呤和8 - 溴环磷酸腺苷(8 BrcAMP)。这些试剂产生的正向诱导作用被8 - 溴环磷酸鸟苷(8 BrcGMP)和前列腺素F2α抑制,这两种物质可能会提高环磷酸鸟苷(cGMP)水平。其他也被证明可诱导Fc受体表达的试剂有脂多糖(LPS)和某些批次的胎牛血清。与cAMP升高剂产生的诱导作用相反,8 BrcGMP和前列腺素F2α无法逆转LPS和胎牛血清所导致的Fc受体表达增加。因此,后一类试剂在产生表型表达变化时可能通过一种性质不同的机制起作用。本研究结果将根据使用肿瘤细胞作为研究淋巴细胞分化的药理学控制的模型系统来进行讨论。