Făgăraşan M O, Eskay R, Axelrod J
National Institute on Alcohol Abuse and Alcoholism, Laboratory of Metabolism and Molecular Biology, Bethesda, MD 20892.
Proc Natl Acad Sci U S A. 1989 Mar;86(6):2070-3. doi: 10.1073/pnas.86.6.2070.
Previous work has shown that corticotropin releasing factor, vasoactive intestinal peptide, phorbol ester, and forskolin cause the secretion of adrenocorticotropic hormone and beta-endorphin from the AtT-20 mouse pituitary cell line. Human recombinant interleukin 1 alpha and 1 beta also stimulated adrenocorticotropic hormone and beta-endorphin secretion from AtT-20 cells in a time- and dose-related manner. The effect appeared only after pretreatment with interleukin 1 (IL-1) for at least 18 hr and was maximum at 24 hr. After pretreatment of the cells over a period of time with IL-1, the secretion induced by corticotropin releasing factor and vasoactive intestinal peptide was increased in more than an additive manner. The enhancement of corticotropin releasing factor-induced beta-endorphin release produced by IL-1 was apparent after 12 hr and reached a maximum at 24 hr. IL-1 did not affect forskolin-induced cAMP generation but enhanced the effect of forskolin on beta-endorphin secretion. This suggests that IL-1 does not induce adenylate cyclase and that forskolin causes the secretion of beta-endorphin by a mechanism independent of cAMP. IL-1 enhanced phorbol ester-induced beta-endorphin secretion. After prolonged treatment with phorbol ester (an activator of protein kinase C), the secretion induced by phorbol ester was abolished as well as the enhancement induced by IL-1. However, prolonged treatment with phorbol ester had no effect on IL-1-induced beta-endorphin secretion. These observations suggest that IL-1 enhances peptide-generated secretion of beta-endorphin by inducing protein kinase C.
先前的研究表明,促肾上腺皮质激素释放因子、血管活性肠肽、佛波酯和福斯高林可促使AtT-20小鼠垂体细胞系分泌促肾上腺皮质激素和β-内啡肽。人重组白细胞介素1α和1β也以时间和剂量相关的方式刺激AtT-20细胞分泌促肾上腺皮质激素和β-内啡肽。该效应仅在白细胞介素1(IL-1)预处理至少18小时后才出现,并在24小时时达到最大值。在用IL-1对细胞进行一段时间的预处理后,促肾上腺皮质激素释放因子和血管活性肠肽诱导的分泌以超过相加的方式增加。IL-1对促肾上腺皮质激素释放因子诱导β-内啡肽释放的增强作用在12小时后明显,并在24小时时达到最大值。IL-1不影响福斯高林诱导的环磷酸腺苷(cAMP)生成,但增强了福斯高林对β-内啡肽分泌的作用。这表明IL-1不诱导腺苷酸环化酶,且福斯高林通过一种独立于cAMP的机制促使β-内啡肽分泌。IL-1增强了佛波酯诱导的β-内啡肽分泌。在用佛波酯(蛋白激酶C的激活剂)进行长时间处理后,佛波酯诱导的分泌以及IL-1诱导的增强作用均被消除。然而,用佛波酯进行长时间处理对IL-1诱导的β-内啡肽分泌没有影响。这些观察结果表明,IL-1通过诱导蛋白激酶C来增强肽生成的β-内啡肽分泌。