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Prion-induced Activation of Cholesterogenic Gene Expression by Srebp2 in Neuronal Cells

机译:re病毒诱导的神经细胞Srebp2致胆源性基因表达的激活。

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摘要

Prion diseases are neurodegenerative diseases associated with the accumulation of a pathogenic isoform of the host-encoded prion protein. The cellular responses to prion infection are not well defined. By performing microarray analysis on cultured neuronal cells infected with prion strain 22L, in the group of up-regulated genes we observed predominantly genes of the cholesterol pathway. Increased transcript levels of at least nine enzymes involved in cholesterol synthesis, including the gene for the rate-limiting hydroxymethylglutaryl-CoA reductase, were detected. Up-regulation of cholesterogenic genes was attributable to a prion-dependent increase in the amount and activity of the sterol regulatory element-binding protein Srebp2, resulting in elevated levels of total and free cellular cholesterol. The up-regulation of cholesterol biosynthesis appeared to be a characteristic response of neurons to prion challenge, as cholesterogenic transcripts were also elevated in persistently infected GT-1 cells and prion-exposed primary hippocampal neurons but not in microglial cells and primary astrocytes. These results convincingly demonstrate that prion propagation not only depends on the availability of cholesterol but that neuronal cells themselves respond to prions with specific up-regulation of cholesterol biosynthesis.
机译:on病毒是与宿主编码的ion病毒蛋白的致病同工型积累有关的神经退行性疾病。对病毒感染的细胞反应尚不明确。通过对感染了ion病毒22L的培养神经元细胞进行微阵列分析,在上调基因组中,我们观察到了胆固醇途径的主要基因。检测到至少九种参与胆固醇合成的酶(包括限速羟甲基戊二酰辅酶A还原酶的基因)的转录水平增加。胆甾醇生成基因的上调归因于固醇调节元件结合蛋白Srebp2的数量和活性的病毒依赖性增加,导致总和游离细胞胆固醇水平升高。胆固醇生物合成的上调似乎是神经元对病毒激发的特征性反应,因为持续感染的GT-1细胞和and病毒暴露的原代海马神经元中胆固醇生成的转录物也升高,但在小胶质细胞和原代星形胶质细胞中却没有。这些结果令人信服地证明that病毒的繁殖不仅取决于胆固醇的可用性,而且神经元细胞本身对病毒的反应是胆固醇生物合成的特定上调。

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