Clinical Toxicology Laboratory (Formerly, Developmental Toxicology Laboratory), Department of Medical Elementology and Toxicology, Jamia Hamdard (Hamdard University), New Delhi 110062, India.
Neurotoxicology. 2013 May;36:24-33. doi: 10.1016/j.neuro.2013.01.008. Epub 2013 Feb 6.
Survival along with optimal proliferation of neuronal precursors determines the outcomes of the endogenous cellular repair in CNS. Cellular-oxidation based cell death has been described in several neurodegenerative disorders. Therefore, this study was aimed at the identification of the potent targets of oxidative damage to the neuronal precursors and its effective prevention by a natural flavonoid, Quercetin. Neuronal precursor cells (NPCs), Nestin+ and GFAP (Glial fibrillary acidic protein)+ were isolated and cultured from adult rat SVZ (subventricular zone). These cells were challenged with a single dose of H2O2 (50μM) and/or pre-treated with different concentrations of Quercetin. H2O2 severely limited the cellular viability and expansion of the neurospheres. Cellular-oxidation studies revealed reduction in glutathione dependent redox buffering along with depletion of enzymatic cellular antioxidants that might potentiate the nitrite (NO2(-)) and superoxide anion (O2(-)) mediated peroxynitrite (ONOO(-)) formation and irreversible protein nitration. We identified depleted PK-M2 (M2 isoform of pyruvate kinase) activity and apoptosis of NPCs revealed by the genomic DNA fragmentation and elevated PARP (poly ADP ribose polymerase) activity along with increased Caspase activity initiated by severely depolarised mitochondrial membranes. However, the pre-treatment of Quercetin in a dose-response manner prevented these changes and restored the expansion of neurospheres preferably by neutralizing the oxidative conditions and thereby reducing peroxynitrite formation, protein nitration and PK-M2 depletion. Our results unravel the potential interactions of oxidative environment and respiration in the survival and activation of precursors and offer a promise shown by a natural flavonoid in the protective strategy for neuronal precursors of adult brain.
神经元前体细胞的存活和最佳增殖决定了中枢神经系统内源性细胞修复的结果。几种神经退行性疾病中都描述了基于细胞氧化的细胞死亡。因此,本研究旨在确定氧化应激对神经元前体细胞的潜在靶标,并通过天然类黄酮槲皮素有效预防其损伤。从成年大鼠 SVZ(侧脑室下区)中分离和培养神经元前体细胞(NPCs)、Nestin+和 GFAP+(神经胶质纤维酸性蛋白)。这些细胞用 50μM 的 H2O2 单一剂量处理,或用不同浓度的槲皮素预先处理。H2O2 严重限制了神经球的细胞活力和扩增。细胞氧化研究显示谷胱甘肽依赖的氧化还原缓冲减少,同时细胞抗氧化酶耗竭,这可能增强亚硝酸盐(NO2-)和超氧阴离子(O2-)介导的过氧亚硝酸盐(ONOO-)形成和不可逆的蛋白质硝化。我们发现 NPCs 的 PK-M2(丙酮酸激酶 M2 同工型)活性耗竭和细胞凋亡,表现为基因组 DNA 片段化和 PARP(多聚 ADP 核糖聚合酶)活性升高,以及线粒体膜严重去极化引发的 Caspase 活性升高。然而,槲皮素以剂量反应方式的预处理可以防止这些变化,并通过中和氧化条件,从而减少过氧亚硝酸盐形成、蛋白质硝化和 PK-M2 耗竭,优先恢复神经球的扩增。我们的结果揭示了氧化环境和呼吸在前体细胞存活和激活中的潜在相互作用,并展示了天然类黄酮在成年大脑神经元前体细胞保护策略中的应用前景。