Instituto de Bioquímica Médica, Programa de Bioquímica e Biofísica Celular, Universidade Federal do Rio de Janeiro, Rio de Janeiro 21944-590, Brazil.
Neurotox Res. 2010 Aug;18(2):112-23. doi: 10.1007/s12640-009-9133-y. Epub 2009 Dec 1.
2,4-Dinitrophenol (DNP) is classically known as a mitochondrial uncoupler and, at high concentrations, is toxic to a variety of cells. However, it has recently been shown that, at subtoxic concentrations, DNP protects neurons against a variety of insults and promotes neuronal differentiation and neuritogenesis. The molecular and cellular mechanisms underlying the beneficial neuroactive properties of DNP are still largely unknown. We have now used DNA microarray analysis to investigate changes in gene expression in rat hippocampal neurons in culture treated with low micromolar concentrations of DNP. Under conditions that did not affect neuronal viability, high-energy phosphate levels or mitochondrial oxygen consumption, DNP induced up-regulation of 275 genes and down-regulation of 231 genes. Significantly, several up-regulated genes were linked to intracellular cAMP signaling, known to be involved in neurite outgrowth, synaptic plasticity, and neuronal survival. Differential expression of specific genes was validated by quantitative RT-PCR using independent samples. Results shed light on molecular mechanisms underlying neuroprotection by DNP and point to possible targets for development of novel therapeutics for neurodegenerative disorders.
2,4-二硝基苯酚(DNP)是一种经典的线粒体解偶联剂,在高浓度下,对多种细胞有毒。然而,最近的研究表明,在亚毒性浓度下,DNP 可以保护神经元免受多种损伤,并促进神经元分化和突起生长。DNP 发挥有益的神经活性特性的分子和细胞机制在很大程度上仍然未知。我们现在使用 DNA 微阵列分析来研究在低毫摩尔浓度的 DNP 处理的大鼠海马神经元培养物中的基因表达变化。在不影响神经元活力、高能磷酸水平或线粒体耗氧量的条件下,DNP 诱导了 275 个基因的上调和 231 个基因的下调。重要的是,几个上调的基因与细胞内 cAMP 信号通路有关,已知该信号通路参与轴突生长、突触可塑性和神经元存活。使用独立样本的定量 RT-PCR 验证了特定基因的差异表达。这些结果揭示了 DNP 神经保护作用的分子机制,并为开发治疗神经退行性疾病的新型治疗方法提供了可能的靶点。