缺氧再氧化过程中一氧化氮对细胞自噬和糖酵解的抑制会损害细胞生物能量并促进原代神经元的细胞死亡。

Free radical biology & medicine Pub Date : 2013-12-01 Epub Date: 2013-09-19 DOI:10.1016/j.freeradbiomed.2013.09.006
Gloria A Benavides, Qiuli Liang, Matthew Dodson, Victor Darley-Usmar, Jianhua Zhang
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引用次数: 45

摘要

已知过量的一氧化氮(NO)产生会损害线粒体蛋白和自噬修复途径,因此可能导致神经毒性。因此,我们假设,在低氧条件下,神经元自噬途径对活性氧和氮类蛋白质损伤的保护可能会被NO破坏,并加剧生物能量功能障碍。大鼠初级皮质神经元在缺氧条件下与正常缺氧条件下具有相同的基础细胞呼吸,而暴露于no的细胞在缺氧条件下线粒体呼吸逐渐减少。再氧化后,一氧化氮处理细胞的呼吸不能恢复到缺氧前的水平。一氧化氮存在下的缺氧-再氧化与自噬抑制有关,自噬抑制剂3-甲基腺嘌呤加重了再氧化过程中无法恢复的情况。缺氧的影响可以通过抑制常压条件下的糖酵解通量来概括。在常氧和低氧条件下,一氧化氮暴露均能立即刺激糖酵解,但长时间的一氧化氮暴露与缺氧条件下线粒体呼吸的不可逆抑制有关,可抑制糖酵解。重要的是,我们发现,只有当培养基中没有葡萄糖或糖酵解被2-脱氧-d-葡萄糖抑制时,一氧化氮才会在常氧条件下抑制基础呼吸,这揭示了一种新的一氧化氮依赖的糖酵解调节的线粒体呼吸抑制机制。综上所述,这些数据表明线粒体呼吸、糖酵解和自噬之间存在氧依赖性相互作用,以保护暴露于NO的神经元细胞。重要的是,他们表明线粒体功能障碍与暴露于NO诱导的糖酵解通量失败密切相关。此外,这些研究为了解自噬和NO如何在神经炎症诱导的细胞损伤中发挥相互作用提供了新的见解,这与我们对过量NO产生的神经退行性疾病病理的理解有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Inhibition of autophagy and glycolysis by nitric oxide during hypoxia-reoxygenation impairs cellular bioenergetics and promotes cell death in primary neurons.

Inhibition of autophagy and glycolysis by nitric oxide during hypoxia-reoxygenation impairs cellular bioenergetics and promotes cell death in primary neurons.

Inhibition of autophagy and glycolysis by nitric oxide during hypoxia-reoxygenation impairs cellular bioenergetics and promotes cell death in primary neurons.

Excessive nitric oxide (NO) production is known to damage mitochondrial proteins and the autophagy repair pathway and so can potentially contribute to neurotoxicity. Accordingly, we hypothesized that protection against protein damage from reactive oxygen and nitrogen species under conditions of low oxygen by the autophagy pathway in neurons would be impaired by NO and enhance bioenergetic dysfunction. Rat primary cortical neurons had the same basal cellular respiration in hypoxia as in normoxia, whereas NO-exposed cells exhibited a gradual decrease in mitochondrial respiration in hypoxia. Upon reoxygenation, the respiration in NO-treated cells did not recover to prehypoxic levels. Hypoxia-reoxygenation in the presence of NO was associated with inhibition of autophagy, and the inability to recover during reoxygenation was exacerbated by an inhibitor of autophagy, 3-methyladenine. The effects of hypoxia could be recapitulated by inhibiting glycolytic flux under normoxic conditions. Under both normoxic and hypoxic conditions NO exposure induced immediate stimulation of glycolysis, but prolonged NO exposure, associated with irreversible inhibition of mitochondrial respiration in hypoxia, inhibited glycolysis. Importantly, we found that NO inhibited basal respiration under normoxic conditions only when glucose was absent from the medium or glycolysis was inhibited by 2-deoxy-d-glucose, revealing a novel NO-dependent mechanism for the inhibition of mitochondrial respiration that is modulated by glycolysis. Taken together these data suggest an oxygen-dependent interaction between mitochondrial respiration, glycolysis, and autophagy in protecting neuronal cells exposed to NO. Importantly, they indicate that mitochondrial dysfunction is intimately linked to a failure of glycolytic flux induced by exposure to NO. In addition, these studies provide new insights into the understanding of how autophagy and NO may play interactive roles in neuroinflammation-induced cellular damage, which is pertinent to our understanding of the pathology of neurodegenerative diseases in which excessive NO is generated.

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