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A Common Carcinogen Benzo[a]pyrene Causes Neuronal Death in Mouse via Microglial Activation

机译:常见的致癌物苯并[a] via通过小胶质细胞激活导致小鼠神经元死亡

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Background Benzo[a]pyrene (B[a]P) belongs to a class of polycyclic aromatic hydrocarbons that serve as micropollutants in the environment. B[a]P has been reported as a probable carcinogen in humans. Exposure to B[a]P can take place by ingestion of contaminated (especially grilled, roasted or smoked) food or water, or inhalation of polluted air. There are reports available that also suggests neurotoxicity as a result of B[a]P exposure, but the exact mechanism of action is unknown. Methodology/Principal Findings Using neuroblastoma cell line and primary cortical neuron culture, we demonstrated that B[a]P has no direct neurotoxic effect. We utilized both in vivo and in vitro systems to demonstrate that B[a]P causes microglial activation. Using microglial cell line and primary microglial culture, we showed for the first time that B[a]P administration results in elevation of reactive oxygen species within the microglia thereby causing depression of antioxidant protein levels; enhanced expression of inducible nitric oxide synthase, that results in increased production of NO from the cells. Synthesis and secretion of proinflammatory cytokines were also elevated within the microglia, possibly via the p38MAP kinase pathway. All these factors contributed to bystander death of neurons, in vitro. When administered to animals, B[a]P was found to cause microglial activation and astrogliosis in the brain with subsequent increase in proinflammatory cytokine levels. Conclusions/Significance Contrary to earlier published reports we found that B[a]P has no direct neurotoxic activity. However, it kills neurons in a bystander mechanism by activating the immune cells of the brain viz the microglia. For the first time, we have provided conclusive evidence regarding the mechanism by which the micropollutant B[a]P may actually cause damage to the central nervous system. In today's perspective, where rising pollution levels globally are a matter of grave concern, our study throws light on other health hazards that such pollutants may exert.
机译:背景技术苯并[a] py(B [a] P)属于一类多环芳烃,在环境中用作微污染物。据报道,B [a] P在人类中可能是致癌物。摄入受污染的(尤其是烤制,烤制或熏制的)食物或水,或吸入污染的空气,可能会接触到B [a] P。有报道表明,由于B [a] P暴露,也会引起神经毒性,但确切的作用机制尚不清楚。方法/主要发现使用成神经细胞瘤细胞系和原代皮层神经元培养,我们证明B [a] P没有直接的神经毒性作用。我们利用体内和体外系统来证明B [a] P引起小胶质细胞活化。使用小神经胶质细胞系和原代小神经胶质细胞培养,我们首次表明B [a] P给药可导致小胶质细胞内活性氧的升高,从而导致抗氧化蛋白水平降低;诱导型一氧化氮合酶表达的增强,导致细胞中NO的产生增加。促炎细胞因子的合成和分泌也可能通过p38MAP激酶途径在小胶质细胞中升高。所有这些因素在体外导致神经元旁观者死亡。当对动物给药时,发现B [a] P会引起大脑中的小胶质细胞活化和星形胶质细胞沉着,并随之增加促炎细胞因子水平。结论/重要性与先前发表的报道相反,我们发现B [a] P没有直接的神经毒性活性。然而,它通过激活大脑的免疫细胞(即小胶质细胞)以旁观者机制杀死神经元。首次,我们提供了有关微污染物B [a] P可能实际上导致中枢神经系统损害的机制的确凿证据。从当今的角度来看,在全球范围内日益严重的污染问题上,我们的研究揭示了此类污染物可能造成的其他健康危害。

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