Wacholtz M C, Minakuchi R, Lipsky P E
Harold C. Simmons Arthritis Research Center, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas 75235.
Cell Immunol. 1991 Jul;135(2):285-98. doi: 10.1016/0008-8749(91)90274-f.
The effect of cyclic AMP-elevating agents on mitogen-stimulated IL2 production was examined. Prostaglandin E2 (PGE2) inhibited IL2 production by human peripheral blood T cells stimulated with PHA. In contrast, PGE2 did not inhibit PHA-stimulated IL2 production by the human leukemic T cell line. Jurkat, and often slightly enhanced IL2 production by those cells. Other cyclic adenosine monophosphate (cAMP) elevating agents (forskolin, isoproterenol, and the cAMP analogue, dibutyryl cAMP) also inhibited lectin-stimulated IL2 production by T cells, but could not inhibit IL2 production by Jurkat cells. Of the cAMP-elevating agents examined, only cholera toxin (CT) inhibited IL2 production by both Jurkat cells and peripheral blood T cells. Although phorbol myristate acetate (PMA) greatly enhanced PHA-stimulated IL2 production by Jurkat cells. CT remained markedly inhibitory. The combination of PMA and the calcium ionophore, ionomycin, also induced IL2 production by Jurkat cells, and this was similarly suppressed by CT, suggesting that a step after initial second messenger generation was inhibited. A prolonged increase in intracellular cAMP levels was induced by CT in both T cells and Jurkat cells, but the maximal level and the length of elevation achieved in T cells were much less than those observed in Jurkat cells. In contrast, PGE2 caused only a modest and transient increase in intracellular cAMP levels in Jurkat cells compared to that noted with T cells. PGE2 induced a more marked and sustained increase in cAMP levels in Jurkat cells treated with isobutylmethylxanthine (IBMX), a phosphodiesterase inhibitor. Moreover, in the presence of IBMX, PGE2 caused a marked inhibition of IL2 production by PHA-stimulated Jurkat cells. Differences in the capacity of PGE2 to induce cAMP could not be explained by disparities in the level of cAMP phosphodiesterase activity as this was comparable in Jurkat cells and in T cells. Thus, these observations indicate that IL2 production by both peripheral T cells and Jurkat cells can be modulated by cAMP-elevating agents. The data suggest that the diminished capacity of PGE2 to inhibit IL2 production by Jurkat cells reflects both a diminished capacity of PGE2 to induce increases in cAMP levels in these cells and an increase in the threshold of cAMP required to inhibit Jurkat cells.
研究了环磷酸腺苷(cAMP)升高剂对丝裂原刺激的白细胞介素2(IL2)产生的影响。前列腺素E2(PGE2)抑制了用植物血凝素(PHA)刺激的人外周血T细胞产生IL2。相比之下,PGE2并不抑制人白血病T细胞系Jurkat细胞由PHA刺激产生的IL2,而且常常会略微增强这些细胞产生IL2的能力。其他环磷酸腺苷(cAMP)升高剂(福斯高林、异丙肾上腺素和cAMP类似物二丁酰cAMP)也抑制T细胞由凝集素刺激产生的IL2,但不能抑制Jurkat细胞产生IL2。在所研究的cAMP升高剂中,只有霍乱毒素(CT)抑制Jurkat细胞和外周血T细胞产生IL2。虽然佛波酯(PMA)极大地增强了Jurkat细胞由PHA刺激产生的IL2,但CT仍然具有明显的抑制作用。PMA和钙离子载体离子霉素的组合也诱导Jurkat细胞产生IL2,而CT同样抑制了这种诱导,这表明在最初的第二信使产生之后的一个步骤受到了抑制。CT在T细胞和Jurkat细胞中均诱导细胞内cAMP水平的持续升高,但T细胞中达到的最大水平和升高的持续时间远低于Jurkat细胞中观察到的情况。相比之下,与T细胞相比,PGE2仅使Jurkat细胞内的cAMP水平有适度且短暂的升高。PGE2在用磷酸二酯酶抑制剂异丁基甲基黄嘌呤(IBMX)处理的Jurkat细胞中诱导cAMP水平有更明显且持续的升高。此外,在存在IBMX的情况下,PGE2显著抑制了PHA刺激的Jurkat细胞产生IL2。PGE2诱导cAMP的能力差异不能用cAMP磷酸二酯酶活性水平的差异来解释,因为Jurkat细胞和T细胞中的该活性相当。因此,这些观察结果表明外周T细胞和Jurkat细胞产生IL2均可受到cAMP升高剂的调节。数据表明,PGE2抑制Jurkat细胞产生IL2的能力减弱既反映了PGE2在这些细胞中诱导cAMP水平升高的能力减弱,也反映了抑制Jurkat细胞所需的cAMP阈值升高。