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白细胞介素-6在MPP+和四氢异喹啉诱导的PC12细胞死亡中的可能作用。

Possible role of interleukin-6 in PC12 cell death induced by MPP+ and tetrahydroisoquinoline.

作者信息

Shimma Naoko, Akiyama Nobuteru, Umezawa Michiko, Okuma Yasunobu, Nomura Yasuyuki, Saito Takeshi, Horie Syunji, Murayama Toshihiko

机构信息

Laboratory of Chemical Pharmacology, Graduate School of Pharmaceutical Sciences, Chiba University, Japan.

出版信息

J Pharmacol Sci. 2003 Dec;93(4):471-7. doi: 10.1254/jphs.93.471.

Abstract

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.

摘要

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。

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