Shimma Naoko, Akiyama Nobuteru, Umezawa Michiko, Okuma Yasunobu, Nomura Yasuyuki, Saito Takeshi, Horie Syunji, Murayama Toshihiko
Laboratory of Chemical Pharmacology, Graduate School of Pharmaceutical Sciences, Chiba University, Japan.
J Pharmacol Sci. 2003 Dec;93(4):471-7. doi: 10.1254/jphs.93.471.
Interleukin (IL)-6 has been shown to protect neuronal cells from cell death induced by various stimulants. Although neuronal cells including PC12 cells were shown to produce IL-6, little is known about the effects of dopaminergic neurotoxins, 1,2,3,4-tetrahydroisoquinoline (TIQ) and 1-methyl-4-phenylpyridinium ion (MPP(+)), on IL-6 expression in PC12 cells. In the present study, we investigated the role of IL-6 in the TIQ- and MPP(+)-induced cell death in PC12 cells. Treatment with 3.2 mM TIQ for 24 h caused a delayed cell death (lactate dehydrogenase (LDH) leakage and nuclear DNA fragmentation) markedly 72 h after the addition. Addition of 0.4 mM MPP(+) caused LDH leakage and nuclear DNA fragmentation 24 h after the addition. The cell death induced by MPP(+) was inhibited by an inhibitor of caspases, z-Val-Ala-Asp(OMe)-fluoromethylketone. The cell death induced by TIQ or MPP(+) was inhibited by nerve growth factor and 10% serum and significantly enhanced by the treatment with anti-IL-6 antibody. Both neurotoxins decreased the IL-6 mRNA level in PC12 cells without changing the other tested mRNA levels (IL-1 alpha, beta-actin, etc.). These findings suggest that dopaminergic neurotoxins cause cell death in PC12 cells at least partially by changing IL-6 expression.
白细胞介素(IL)-6已被证明可保护神经元细胞免受各种刺激物诱导的细胞死亡。尽管包括PC12细胞在内的神经元细胞已被证明可产生IL-6,但关于多巴胺能神经毒素1,2,3,4-四氢异喹啉(TIQ)和1-甲基-4-苯基吡啶离子(MPP(+))对PC12细胞中IL-6表达的影响知之甚少。在本研究中,我们研究了IL-6在TIQ和MPP(+)诱导的PC12细胞死亡中的作用。用3.2 mM TIQ处理24小时会导致延迟性细胞死亡(乳酸脱氢酶(LDH)泄漏和核DNA片段化),在添加后72小时明显出现。添加0.4 mM MPP(+)会在添加后24小时导致LDH泄漏和核DNA片段化。MPP(+)诱导的细胞死亡被半胱天冬酶抑制剂z-Val-Ala-Asp(OMe)-氟甲基酮抑制。TIQ或MPP(+)诱导的细胞死亡被神经生长因子和10%血清抑制,并通过用抗IL-6抗体处理而显著增强。两种神经毒素均降低了PC12细胞中IL-6 mRNA水平,而不改变其他测试的mRNA水平(IL-1α、β-肌动蛋白等)。这些发现表明,多巴胺能神经毒素至少部分通过改变IL-6表达导致PC12细胞死亡。