Buchmüller-Rouiller Y, Betz-Corradin S, Mauël J
Institute of Biochemistry, Epalinges, Switzerland.
J Immunol. 1992 Feb 15;148(4):1171-5.
Calcium ionophore A23187 can mimic IFN-gamma-induced macrophage activation for intracellular Leishmania killing and secretion of L-arginine-derived nitrite. Because the effects of ionophore are not restricted to calcium mobilization but also involve alterations of phospholipid metabolism, we have examined the role of PGE2 in the activation process. Macrophages exposed to A23187 or IFN-gamma in the presence of LPS and FCS secreted significant amounts of PGE2 independently of the presence of L-arginine in the incubation medium. The addition of the cyclooxygenase inhibitor indomethacin or omission of FCS abrogated PGE2 secretion but had little effect on nitrite production or intracellular killing. The addition of exogenous PGE2, of agents increasing PGE2 production such as arachidonic acid and colchicine, or of an analogue of cAMP, dibutyryl cAMP inhibited A23187 + LPS-induced activation whereas that mediated by IFN-gamma + LPS remained unimpaired. Our results indicate that PGE2 can modulate activation induced by A23187 but not by IFN-gamma, probably by a process involving cAMP. Conceivably, ionophore can mimic IFN-gamma for the induction of activation but lacks the capacity to help maintain the activated state because of its inability to desensitize macrophages to negative regulation by PGE2, as suggested previously for IFN-gamma-dependent activation.
钙离子载体A23187可模拟γ干扰素诱导的巨噬细胞活化,以杀伤细胞内利什曼原虫并分泌L-精氨酸衍生的亚硝酸盐。由于离子载体的作用不仅限于钙离子动员,还涉及磷脂代谢的改变,因此我们研究了前列腺素E2(PGE2)在活化过程中的作用。在脂多糖(LPS)和胎牛血清(FCS)存在的情况下,暴露于A23187或γ干扰素的巨噬细胞会分泌大量PGE2,这与孵育培养基中L-精氨酸的存在无关。添加环氧化酶抑制剂吲哚美辛或去除FCS可消除PGE2的分泌,但对亚硝酸盐的产生或细胞内杀伤作用影响不大。添加外源性PGE2、增加PGE2产生的试剂(如花生四烯酸和秋水仙碱)或环磷酸腺苷(cAMP)类似物二丁酰cAMP可抑制A23187 + LPS诱导的活化,而γ干扰素+ LPS介导的活化则不受影响。我们的结果表明,PGE2可能通过涉及cAMP的过程调节由A23187诱导的活化,但不调节由γ干扰素诱导的活化。可以想象,离子载体可以模拟γ干扰素诱导活化,但由于其无法使巨噬细胞对PGE2的负调节脱敏,因此缺乏维持活化状态的能力,正如先前对γ干扰素依赖性活化所建议的那样。